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̼Æ×Êý¾Ý ÈçÏ »¯ºÏÎï1 209.86, 76.37, 49.45, 41.52, 39.05, 33.53, 30.87, 30.75, 28.73, 18.23, 17.02, 15.41, 15.23, 14.64, 11.19 »¯ºÏÎï2 141.79, 134.09, 126.01, 112.15, 83.37, 78.19, 50.77, 47.25, 34.96, 33.19, 29.71, 27.10, 22.32, 21.86. [ Last edited by chzhbin on 2012-5-10 at 13:05 ] |
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»¯ºÏÎï1 ²éѯ½á¹û£º¹²²éµ½76¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (1S,4S,5S,6R,7S,10S)-dihydroxymaaliane C15H26O2 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2000 48(11) 77-80 Three New Sesquiterpenoid Glucosides of Ficus pumila Fruit Junichi KITAJIMA,Kaoru KIMIZUKA,and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 10¦Î-hydroxy-isocampheren-11-ene C15H24O ÏàËÆ¶È:66.6% Phytochemistry 1999 50 1213-1218 Santalane and isocampherenane sesquiterpenoids from Illicium tsangii Koon-Sin Ngo, Geo}rey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Allo-aromadendrane-10 ¦Á,14-diol C15H26O2 ÏàËÆ¶È:66.6% Archives of Pharmacal Research 2008 31 21-27 A new sesquiterpene and other terpenoid constituents of Chisocheton penduliflorus Jarinporn Phongmaykin, Takuya Kumamoto, Tsutomu Ishikawa, Rutt Suttisri and Ekarin Saifah Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (1S,10S)-9¦Á-hydroxy-allo-aromadendrane C15H26O ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (1R,10R)-9¦Â-hydroxyaromadendrane C15H26O ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (1R,10R)-aromadendran-9-one C15H24O ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (1R,10R)-13-hydroxyaromadendr-9-one C15H24O2 ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 2¦Â,9¦Â-dihydroxyaromadendr-1(10)-ene C15H24O2 ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 2¦Â,9¦Á-dihydroxyaromadendr-1(10)-ene C15H24O2 ÏàËÆ¶È:60% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 2a C15H22O3 ÏàËÆ¶È:60% Journal of Natural Products 2004 67 31-36 Africane-Type Sesquiterpenoids from the Argentine Liverwort Porella swartziana and Their Antibacterial Activity Graciela Bovi Mitre, Norma Kamiya, Alicia Bardn, and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . maadiol ÏàËÆ¶È:60% Phytochemistry 1992 31 3511-3514 Sesquiterpenoids and iridoid glycosides from Valeriana fauriei Koichi Nishiya, Takefumi Kimura, Koichi Takeya, Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 4¦Á,7¦Â-dihydroxy-10¦ÂH-guai-5-en-1¦Â,8¦Â-endoxide C15H24O3 ÏàËÆ¶È:60% Molecules 2011 16 518-522 A New Sesquiterpene with a Novel 1¦Â, 8¦Â-Oxygen Bridge from Heteropappus altaicus (willd.) Novopokr. Yi-Feng Han, Xiao-Jing Gao and Hai Huang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (1 S,13S,15S,28S)-2,12,14,14,29,29-Hexamethyl-18,25-dioxa-3,4,10,11-tetraazatricyclo[26.1.1.1(13,15)]hentriaconta-2,11-dien-5,9,19,24-tetrone ÏàËÆ¶È:56.2% Chemistry of Natural Compounds 2011 Vol. 47, No. 2 210-214 SYNTHESIS FROM (+)-¦Á-PINENE OF OPTICALLY ACTIVE MACROCYCLES CONTAINING CYCLOBUTANE, ESTER,AZINE, OR HYDRAZIDE GROUPS G. Yu. Ishmuratov,G. R. Mingaleeva, O. O. Shakhanova,R. R. Muslukhov, M. P. Yakovleva, L. P. Botsman,and A. G. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (1S,13S,15S,28S)-2,12,14,14,29,29-hexamethyl-18,25-dioxa-3,4,10,11-tetraazatricyclo[26.1.1.1(13,15)]-hentriaconta-2,11-diene-5,9,19,24-tetraone ÏàËÆ¶È:56.2% Russian Journal of Organic Chemistry 2011 47 1416-1425 Synthesis of macrocyclic azino and dihydrazido diesters by consecutive [2 + 1]- and [1 + 1]-condensations G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, O. O. Shakhanova and R. R. Muslukhov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . dendronobilin H C15H26O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2007 Vol. 90 2386 Nine New Sesquiterpenes from Dendrobium nobile Xue Zhanga)b)c), Hong-Wei Liud), Hao Gaoa)b)c), Hui-Ying Hane), Nai-Li Wangb)e), Hou-Ming Wuf), Xin-Sheng Yaoe), and Zhao Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ent-4-epi-maaliol C15H26O ÏàËÆ¶È:53.3% Phytochemistry 2005 66 599-609 Sesquiterpene constituents from the essential oil of the liverwort Plagiochila asplenioides Adewale Martins Adio, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (4S)-3¦Á,10¦Á,12,15-tetrahydroxycadinane ÏàËÆ¶È:53.3% Phytochemistry 2002 59 479-488 Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740 Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 2¦Â-hydroxyaromadendr-1(10)-en-9-one ÏàËÆ¶È:53.3% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (1S,10S)-1¦Á,2¦Â,9¦Â, 10btetrahydroxyaromadendrane C15H26O4 ÏàËÆ¶È:53.3% Phytochemistry 2002 60 475-481 Aromadendrane transformations by Curvularia lunata ATCC 12017 Dwight O. Collins, William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . [1RS,2RS,5E,9SR,10RS]-1,5,8,8-tetramethylbicyclo[8.1.0]undec-5-ene-2,9-diol C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2005 68 1441-1442 A Stable Rearrangement Product of Humulene-4,5-epoxide Raymond M. Carman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 1¦Â,7¦Á-dihydroxyeudesman-4(15)-ene C15H26O2 ÏàËÆ¶È:53.3% Planta Medica 2005 71 268-272 New Sesquiterpenes from Erigeron annus Li, Xin; Yang, Min; Han, Yi-Feng; Gao, Kun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . compound 1 ÏàËÆ¶È:53.3% Phytochemistry 2000 55 749-753 The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . N-ethylisocarvomenthylamine ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 1980 16 397-402 SYNTHESIS AND STUDY OF THE STRUCTURE OF NEW N-SUBSTITUTED 2-METHYL-5-(1-METHYLETHYL)CYCLOHEXYLAMINES I. I, Bardyshev, N. G. Kozlov, T. K. Vyalimyae, and T. I. Pekhk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . N-propylisocarvomenthylamine ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 1980 16 397-402 SYNTHESIS AND STUDY OF THE STRUCTURE OF NEW N-SUBSTITUTED 2-METHYL-5-(1-METHYLETHYL)CYCLOHEXYLAMINES I. I, Bardyshev, N. G. Kozlov, T. K. Vyalimyae, and T. I. Pekhk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 8-oxo eremophila-6,9-dien-12-oic acid ÏàËÆ¶È:53.3% Chinese Chemical Letters 1998 9 61-64 Eremophilane Sesquiterpenes from Cacalia Roborowskii Suo Ming ZHANG,Gui Ling ZHAO,Rong LI and Guo Qiang LIN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 1¦Â,7¦Á-dihydroxyeudesma-4(15)-en C15H26O2 ÏàËÆ¶È:53.3% Chinese Chemical Letters 2005 16 61-63 New Eudesmenes from Erigeron annus Xin LI, Qiu Hong WU, Kun GAO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 1,1,3,4,6-Pentamethyl-4a,5,6,7,8,8a-hexahydro-1H-isochromene ÏàËÆ¶È:53.3% Molecules 2009 14 2780-2800 Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® Laura Chapado, Pablo J. Linares-Palomino, Concepci¨®n Bad¨ªa, Sof¨ªa Salido, Manuel Nogueras, Adolfo S¨¢nchez and Joaqu¨ªn Altarejos Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . pterodontriol E C15H28O3 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2006 8 303-307 Two eudesmane sesquiterpenes from Laggera pterodonta Y.-B. LIU, W. JIA, W.-Y. GAO, A.-H. ZHAO, Y.-W. ZHANG, Y. TAKAISHI and H.-Q. DUAN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . (-)-ledol C15H26O ÏàËÆ¶È:53.3% Natural Product Research 2000 14 447-452 (-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . compound 1b ÏàËÆ¶È:53.3% Natural Product Research 2000 14 447-452 (-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . ¦Á-santal-11-ene-10-one C15H22O ÏàËÆ¶È:53.3% Phytochemistry 1999 50 1213-1218 Santalane and isocampherenane sesquiterpenoids from Illicium tsangii Koon-Sin Ngo, Geo}rey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . 11-hydroxy-isocampheren-9-ene ÏàËÆ¶È:53.3% Phytochemistry 1999 50 1213-1218 Santalane and isocampherenane sesquiterpenoids from Illicium tsangii Koon-Sin Ngo, Geo}rey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . isocampheren-11-ene-10-one C15H24O2 ÏàËÆ¶È:53.3% Phytochemistry 1999 50 1213-1218 Santalane and isocampherenane sesquiterpenoids from Illicium tsangii Koon-Sin Ngo, Geo}rey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 8-Oxo-eremophila-6,9-dien-12-oic acid C15H20O3 ÏàËÆ¶È:53.3% Phytochemistry 1998 48 519-524 Eremophilane sesquiterpenes from Cacalia roborowskii Suoming Zhang, Guiling Zhao, Rong Li, Guoquiang Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . (¡À)-[1S-(1¦Â,4¦Â,4a¦Â,6¦Á,8a¦Á)]-1,6-Dimethyl-4-(1-methylethyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-1,6-naphthalenediol ÏàËÆ¶È:53.3% Phytochemistry 1996 42 1097-1103 Three new oxygenated cadinanes from Baccharis species Carmen L. Queiroga, Vera L. Ferracini, A. J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . (11S)-5¦ÂH-eudesmane-3¦Á,13-diol C15H28O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1994 Vol 57 1189 Synthetic Studies of Sesquiterpenes with a cis-Fused Decalin System, 4. Synthesis of (+)-5¦ÂH-Eudesma-3,11-diene, (-)-5¦ÂH-Eudesmane-4¦Â,11-diol, and (+)-5¦ÂH-Eudesmane-4¦Á,11-diol, and Structure Revision of a Natural Eudesmane-4,11-diol Isolated from Pluchea Masayoshi Ando, Koji Arai, Kazuhira Kikuchi, Koji Isogai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . ptychanolide ÏàËÆ¶È:53.3% Phytochemistry 1993 32 335-348 Terpenoids of the liverwort Frullanoides densifolia and Trocholejeunea sandvicensis Motoo Tori, Hernita Arbiyanti, Zenei Taira, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . tamariscol ÏàËÆ¶È:53.3% Phytochemistry 1991 30 2295-2300 Geographical distribution of tamariscol, a mossy odorous sesquiterpene alcohol, in the liverwort Frullania tamarisci and related species Yoshinori Asakawa, Masakazu Sono, Mariko Wakamatsu, Keiko Kondo, Sinske Hattori, Masami Mizutani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . (1S,6S,8S,21S)-2,5,7,7,22,22-Hexamethyl-11,18-dioxa-3,4-diazatricyclo[19.1.1.1(6,8)]tetracosa-2,4-dien-12,17-dione ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2011 Vol. 47, No. 2 210-214 SYNTHESIS FROM (+)-¦Á-PINENE OF OPTICALLY ACTIVE MACROCYCLES CONTAINING CYCLOBUTANE, ESTER,AZINE, OR HYDRAZIDE GROUPS G. Yu. Ishmuratov,G. R. Mingaleeva, O. O. Shakhanova,R. R. Muslukhov, M. P. Yakovleva, L. P. Botsman,and A. G. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . (2S,3R)-Diethyl-2-(cyclobutylmethyl)-3-hydroxy-2-methylsuccinate C14H24O5 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2011 19 2696-2706 Geminal dialkyl derivatives of N-substituted pantothenamides: Synthesis and antibacterial activity T. Olukayode Akinnusi, Kenward Vong, Karine Auclair Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . Dihydro-¦Á-santaldiol C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 2012 77 304-311 ¦Á-Santalol derivatives from Santalum album and their cytotoxic activities Yukiko Matsuo ,Yoshihiro Mimaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . compound 2 ÏàËÆ¶È:53.3% Tetrahedron Letters 2000 41 2737-2740 Diastereodivergent synthesis of the C8¨CC18 precursor and C1¡ä¨CC11¡ä subunit of pamamycin 607 induced by a chiral sulfoxide group Guy Solladi¨¦, Xavier J. Salom-Roig, Gilles Hanquet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . mandassidione C15H22O2 ÏàËÆ¶È:53.3% Phytochemistry 1988 27 3319-3321 Mandassidione and other sesquiterpenic ketones from Cyperus articulatus B. Nyasse,R. Ghogomu,Tih B.L. Sondengam,M. T. Martin,B. Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . bis-(Dimethyldithiocarbamyl)thioethyl-¦Á-diethylphosphoryl- methane C13H27N2O3PS5 ÏàËÆ¶È:53.3% Journal of Heterocyclic Chemistry 2005 42 103-108 An approach to biologically important S-heterocycles,dithiocarbamyls,and their relevant phosphono derivatives Maha D. Khidre,Azza A. Kamel and Wafaa M. Abdou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . ethyl 2-diazo-4-[(1R)-1,3,3-trimethyl-2-methylenecyclohexyl]-3-oxobutanoate ÏàËÆ¶È:53.3% Indian Journal of Chemistry 2009 48B 413-422 Enantiospecific total synthesis of ent-10,11-thapsan-10-ol Srikrishna,A; Anebouselvy,K Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . Compound 14 ÏàËÆ¶È:53.3% Magnetic Resonance in Chmesitry 2003 41 1034-1037 Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . Dihydro-¦Á-santalen-12-one C15H24O ÏàËÆ¶È:53.3% Phytochemistry 1984 23 595-597 Sesquiterpenes from severinia buxifolia Wu Tian-Shung, Masatake Niwa, Hiroshi Furukawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . compound 4 ÏàËÆ¶È:53.3% Phytochemistry 1984 23 1647-1649 Oxidized aristolane sesquiterpenes from Aristolochia debilis Gerhard R¨¹cker, Ralf Mayer, Eberhard Breitmaier, Georg Will, Armin Kirfel, Mohamed El Kordy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . Terebinthene ÏàËÆ¶È:53.3% Phytochemistry 2010 71 1371-1374 Spirocyclopropane-type sesquiterpene hydrocarbons from Schinus terebinthifolius Raddi Rita Richter, Stephan H. von Reuß, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . ptychanolide C15H22O3 ÏàËÆ¶È:53.3% Tetrahedron letters 1981 22 5307-5310 Ptychanolide, a sesquiterpenoid with a new type skeleton from the liverwort ptychanthus striatus (lehm. et lindenb.) nees Reiji Takeda, Hideo Naoki, Takashi Iwashita, Yoshio Hirose Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . 1¦Â,5¦Á-dihydroxy-11¦ÁH-eudesma-4(15)-en-12,8¦Â-olide C15H22O4 ÏàËÆ¶È:53.3% Tetrahedron 2010 66 9379-9388 New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages Jiang-Jiang Qin, Hui-Zi Jin, Jia-Xian Zhu, Jian-Jun Fu, Qi Zeng, Xiang-Rong Cheng, Yan Zhu, Lei Shan, Shou-De Zhang, Yue-Xing Pan, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 52 . (-)-10(R)-hydroxyalloaromadendrane C15H26O ÏàËÆ¶È:53.3% Tetrahedron 1996 52 2359-2368 Terpenoids with antifouling activity against barnacle larvae from the marine sponge Acanthella cavernosa Hiroshi Hirota, Yasuhiko Tomono, Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 53 . (4S,2'S,3'S)-3-(3'-azido-2'-methylpentyl)-4-isopropyl-2-oxazolidinone C13H22N2O3 ÏàËÆ¶È:53.3% The Journal of Organic Chemistry 2002 67 1760-1767 Kulokekahilide-1, a Cytotoxic Depsipeptide from the Cephalaspidean Mollusk Philinopsis speciosa Junji Kimura, Yuuki Takada, Tomoko Inayoshi, Yoichi Nakao, Gilles Goetz, Wesley Y. Yoshida, and Paul J. Scheuer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 54 . 9¦Â-hydroxy-6,7¦ÁH,11¦ÂH-eudesm-4-en-6,12-olide ÏàËÆ¶È:53.3% Tetrahedron 1995 51 5609-5616 Synthesis of 9-oxyfunctionalized eudesmanes from artemisin Victoria Bargues, Gonzalo Blay, Begoña Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 55 . allohimachalol C15H26O ÏàËÆ¶È:53.3% Tetrahedron 1999 55 759-770 Allohimachalane, seco-allohimachalane and himachalane sesquiterpenes from Illicium tsangii Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 56 . (1S,6S,8S,21S)-2,5,7,7,22,22-hexamethyl-11,18-dioxa-3,4-diazatricyclo[19.1.1.1(6,8)]tetracosa-2,4-diene-12,17-dione ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2011 47 1416-1425 Synthesis of macrocyclic azino and dihydrazido diesters by consecutive [2 + 1]- and [1 + 1]-condensations G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, O. O. Shakhanova and R. R. Muslukhov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 57 . peribysin F C15H26O4 ÏàËÆ¶È:53.3% The Journal of Antibiotics 2005 58 185-191 Absolute Stereostructures of Cell-adhesion Inhibitors, Peribysins A, E, F and G, Produced by a Sea Hare-derived Periconia sp. FREE Takeshi Yamada, Mitsunobu Doi, Atsuko Miura, Waka Harada, Mika Hiramura, Katsuhiko Minoura, Reiko Tanaka and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 58 . 6¦Â-Hydroxypathoulol C15H26O2 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2011 94 218-223 New Patchoulol-Type Sesquiterpenoids from Pogostemon cablin Lei Zhou, Min Xu, Chong-Ren Yang, Yi-Fei Wang and Ying-Jun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 59 . compound 2a ÏàËÆ¶È:52.9% Chemical & Pharmaceutical Bulletin 2006 54 1370-1379 Studies on Nepalese Crude Drugs. XXIX. Chemical Constituents of Dronapuspi, the Whole Herb of Leucas cephalotes SPRENG. Yukinori Miyaichi, Akiko Segawa and Tsuyoshi Tomimori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 60 . Stanozolol ÏàËÆ¶È:52.9% Steroids 1992 57 537-550 17-Epimerization of 17¦Á-methyl anabolic steroids in humans: metabolism and synthesis of 17¦Á-hydroxy-17¦Â-methyl steroids Willi Schänzer, Georg Opfermann, Manfred Donike Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 61 . 3¦Á,4¦Á-dihydroxyclerodan-15-oic acid C20H36O4 ÏàËÆ¶È:50% Helvetica Chimica Acta 2003 Vol. 86 3187 Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 62 . 3¦Á,4¦Á-dihydroxyclerodan-15-oic acid C20H36O4 ÏàËÆ¶È:50% Helvetica Chimica Acta 2003 Vol. 86 3187 Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 63 . ketone C18H30O ÏàËÆ¶È:50% Journal of Natural Products 1997 60 1261-1264 Cyclic Peroxides and Related Norterpenes from a Southern Australian Marine Sponge, Mycale sp. Robert J. Capon, Simone J. Rochfort, and Simon P. B. Ovenden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 64 . [(1aR,3aR,4S,5R,7aR,7bS)-Decahydro-4,5,7¦Á,7¦Â-tetramethylnaphtho[1,2-b]oxiren-4-yl]acetaldehyde C16H26O2 ÏàËÆ¶È:50% Chemistry & Biodiversity 2009 6 447-458 Structure¨C Activity Relationship Studies on the Mosquito Toxicity and Biting Deterrency of Callicarpenal Derivatives Charles L. Cantrell, Jerome A. Klun, Julia Pridgeon, James Becnel, Solomon Green III, and Frank R. Fronczek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 65 . 5,6¦Á-cyclopropano-5¦Á-androst-7-ene-3,17-dione C20H26O2 ÏàËÆ¶È:50% Steroids 2000 65 863-870 Microbial transformation of 3-hydroxy-5,6-cyclopropanocholestanes - An alternative route to 6-methylsteroids Jiann-Long Yan, Shoei-Sheng Lee, K. C. Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 66 . compound 2c ÏàËÆ¶È:50% Journal of Natural Products 1984 Vol 47 592-599 Cmr Spectroscopy of Labdanic Diterpenes and Related Substances Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 67 . compound 19a ÏàËÆ¶È:50% Journal of Natural Products 1984 Vol 47 592-599 Cmr Spectroscopy of Labdanic Diterpenes and Related Substances Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 68 . 16-(furan-2-ylmethylene)-5¦Á-androstan-3,17-dione C24H30O3 ÏàËÆ¶È:50% Steroids 2011 76 709-723 Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 69 . lagaspholone A C20H28O3 ÏàËÆ¶È:50% Organic Letters 2007 Vol. 9, No. 3 489-492 Lagaspholones A and B: Two New Jatropholane-Type Diterpenes from Euphorbia lagascae No¨¦lia Duarte and Maria-Jos¨¦ U. Ferreira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 70 . ¦Â-himachalene C16H24Cl2O3 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2004 59b 1177-1179 Synthesis, Structure, and Absolute Configuration of a New Cyclopropanic Compound Derived from the Sesquiterpene ¦Â-Himachalene Hossni Ziyat, Soufiane El Houssame, Mustapha Ait Ali, My Youssef Ait Itto, Abdellah Karim, RudolfWartchow, and Holger Butenschön Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 71 . (4R,8R,9R)-8-methoxyisocaryolane-9,15-diol C16H28O3 ÏàËÆ¶È:50% Journal of Natural Products 2011 74 1707-1712 Biotransformation of Bioactive Isocaryolanes by Botrytis cinerea Jociani Ascari, Maria Am elia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur an-Patr on, Rosario Hern andez-Gal an, Antonio J. Mac¨ªas-S anchez, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 72 . compound 9 ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 5669-5672 Total synthesis of (¡À)-nakamurol-A and its 13-epimer: tentative assignment of the C-13 relative configuration Josep Bonjoch, Javier Cuesta, Sandra D¨ªaz, Asensio Gonz¨¢lez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 73 . compound 25 ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 6643-6647 An enantiospecific approach to thapsanes from R-carvone: synthesis of (− -thaps-8-en-5-olA. Srikrishna, K. Anebouselvy, T. Jagadeeshwar Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 74 . (1R,3S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3,6,10,10-tetramethyltricyclo[4.4.0.01,3]decan-4-one C20H36O2Si ÏàËÆ¶È:50% Indian Journal of Chemistry 2008 47B 449-459 Enantiospecific synthesis of thaps-8-en-5-ol via stereospecific Srikrishna,A; Anebouselvy,K Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 75 . cis-3-(2-Undecylcyclopropyl)propionic acid C17H32O3 ÏàËÆ¶È:50% Molecules 2011 16 9972-9982 Isolation of C11 Compounds and a Cyclopropane Fatty Acid from an Okinawan Ascidian, Diplosoma sp. Tamanna Rob, Takayuki Ogi, Wilmar Maarisit, Junsei Taira and Katsuhiro Ueda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 76 . isothiocyanate 1 ÏàËÆ¶È:50% Natural Product Research and Development 2003 15 199-202 STUDIES ON THE CHEMICAL CONSTITUENTS OF MARINE SPONGE ACANTHELLASP.FROM THE SOUTH CHINA SEA YAN Xiao-hong; SONG Guo-qiang; ZHOU Xiu-hong; LIU Song-bai; GUO Yue-wei Structure 13C NMR ̼Æ×Ä£Äâͼ |
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»¯ºÏÎï2 ²éѯ½á¹û£º¹²²éµ½90¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . suberosol C C15H24O ÏàËÆ¶È:60% Journal of Natural Products 2002 65 887-891 Suberosols A-D, Four New Sesquiterpenes with ¦Â-Caryophyllene Skeletons from a Taiwanese Gorgonian Coral Subergorgia suberosa Guey-Horng Wang, Atallah F. Ahmed, Jyh-Horng Sheu, Chang-Yih Duh, Ya-Ching Shen, and Li-Tang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 11 ÏàËÆ¶È:58.8% Tetrahedron 1991 47 9411-9418 New examples of acyclic and cyclic C-15 acetogenins from laurencia pinnatifida. Reassignment of the absolute configuration for E and Z pinnatifidienyne. Manuel Noite, Antonio G. Gonzalez, Fernando Cataldo, Mat¨ªas L. Rodr¨ªguez, Ivan Brito Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3,3,6,6-Tetramethyl-9-(2-nitrophenyl)-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-dione C23H26N2O4 ÏàËÆ¶È:57.1% Molecules 2009 14 1468-1474 An Efficient One-Pot Three-Component Synthesis of Fused 1, 4-Dihydropyridines Using HY-Zeolit Mohammad Nikpassand, Manouchehr Mamaghani and Khalil Tabatabaeian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 5 C15H22O2 ÏàËÆ¶È:57.1% Chemical Journal of Chinese Universities 2009 30 1329-1331 First Asymmetric Synthesis of (7R, 10S)-Boivinianin B XU Bo-Yan, SONG Na, LIWen-Ze, XIN Zhi-Jun, LIYing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 5-Cyanotetralin C11H11N ÏàËÆ¶È:57.1% Canadian Journal of Chemistry 2006 84 10-20 Steric effects in the phototransposition reactions of dialkylbenzenes C.M. Gonzalez and J.A. Pincock Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 1-Methyl-2-{[(1R,2S,5R)-6,6-dimethylbicyclo[3.1.1]heptyl-2]methylsulfonyl}-1H-imidazole C14H22N2O2S ÏàËÆ¶È:57.1% Chemistry of Natural Compounds 2012 48 38-42 SYNTHESIS OF NEW MONOTERPENE SULFONYLIMIDAZOLES M. Ya. Demakova,D. V. Sudarikov,S. A. Rubtsova,L. L. Frolova,and A. V. Kuchin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Methyl (1R*,2R*,10 R*)-1,10-Dimethyl-7-oxo-bicyclo[4.4.0]dec-5-ene-2-carboxylate C14H20O3 ÏàËÆ¶È:57.1% Journal of the Chemical Society, Perkin Transactions 1 1991 1919-1922 Total synthesis of kanshone A, a sesquiterpene isolated from Nardostachys chinensis (Valerianaceae) Motoo Tori, Hirosuke Furuta and Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3,3,6,6-Tetramethyl-9-(2-nitrophenyl)-3,4,6,7,9,10-hexahydroacridine-1,8(2H,5H)-dione C23H26N2O4 ÏàËÆ¶È:57.1% Chinese Chemical Letters 2011 22 531-534 Multicomponent synthesis of dihydropyridines catalyzed by l-proline Leila Zare, Mohammad Nikpassand Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 1-Methyl-2-[((1S,2S,5R)-2-isopropyl-5-methylcyclohexyl)sulfanyl]-1H-imidazole C14H24N2S ÏàËÆ¶È:57.1% Chemistry of Natural Compounds 2012 47 899-902 Synthesis of neomenthylsulfanylimidazoles M. Ya. Demakova, D. V. Sudarikov, S. A. Rubtsova, P. A. Slepukhin and A. V. Kuchin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (2R,5R,10S)-2-N-methyl-6-axene C16H29N ÏàËÆ¶È:56.2% Tetrahedron 2006 62 10393-10399 Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa Christopher J. Wegerski, Rachel N. Sonnenschein, Freddy Cabriales, Frederick A. Valeriote, Teatulohi Matainaho, Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (3e,5e)-3,7,11-trimethyl-9-oxododeca-1,3,5-triene C15H24O ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 401-405 New Acyclic Sesquiterpenes and Norsesquiterpenes from the Caribbean Gorgonian Plexaurella grisea Ana Rueda, Eva Zub¨ªa, Mar¨ªa J. Ortega, and Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 9¦Á,15-dihydroxyafricanane C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 1019-1021 New Oxygenated Africanenes from the Soft Coral Sinularia dissecta P. Ramesh, N. Srinivasa Reddy, T. P. Rao, and Y. Venkateswarlu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . clovan-2¦Á,9¦Â-diol C16H28O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 1348-1351 The Biotransformation of Some Clovanes by Botrytis cinerea Isidro G. Collado, James R. Hanson, Antonio J. Mac¨ªas-S¨¢nchez, and D. Mobbs Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3,10-Epoxygermacr-4(14)-en-8-one C15H24O2 ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 1991 27 20-24 NEW TERPENOIDS OF THE ESSENTIAL OIL OF LEDUM PALUSTRE N. I. Belousova, A. V. Tkachev,M. M. Shakirov, and V. A. Khan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . cytotoxic sesquiterpene caryol-7-en-6-ol ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2009 92 375-378 A New Tricyclo[6.3.1.02,5]dodecane Sesquiterpene from Cultures of the Basidiomycete Campanella junghuhnii Rong Liu, Zhong-Yu Zhou, Di Xu, Fei Wang, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ( 1R*,4R*,5Z,9S*)-5-isopropyl-3,3,9-trimethylbicyclo[4. 3.0]nona-5-en-4-ol C15H26O ÏàËÆ¶È:53.3% Journal of Natural Products 1991 Vol 54 1025 New Sesquiterpenes and C15 Acetogenins from the Marine Red Alga Laurencia implicata Anthony D. Wright, Gabriele M. König, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 4-hydroxy-5-brasilene C15H26O ÏàËÆ¶È:53.3% Phytochemistry 1991 30 1921-1927 Brasilane-type sesquiterpenoids from the mediterranean red alga Laurencia obtusa Vincenzo Amico, Salvatore Caccamese, Placido Neri, Giusy Russo, Mario Foti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . isodauc-7(14)-en-6¦Á,10¦Â-diol C15H26O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2010 58 991-994 Sesquiterpenoids and Other Constituents from Senecio argunensis Wei-Dong Xie, Yu-Fang Niu, Peng-Xiang Lai and Kyung-Ho Row Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 2-chloro-3-hydroxy-¦Á-chamigren-9-one C15H23ClO2 ÏàËÆ¶È:53.3% Phytochemistry 1987 26 1053-1057 Chamigrane metabolites from a Jamaican variety of laurencia obtusa Mary R. Brennan,Karen L. Erickson,Donna A. Minott,Keith O. Pascoe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 12aii C15H17NOS ÏàËÆ¶È:53.3% Journal of Heterocyclic Chemistry 2005 42 201-207 Intramolecular photoreactions of thiohomophthalimides with an alkenyl group in their N-Side chain. Regioselective synthesis of heterocycle-fused isoquinoline derivatives through [2+2] photocycloaddition Haruko Takechi,Hajime Takahashi and Minoru Machida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 5d C15H24O2 ÏàËÆ¶È:53.3% Tetrahedron Letters 2005 46 5803-5806 TiF4-mediated biomimetic alkylation-cyclization cascade reaction of 2-trimethylsilylmethyl-1,5-dienes with aldehydes Luigi Anastasia, Elios Giannini, Giuseppe Zanoni, Giovanni Vidari Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . compound 4a C15H24O2 ÏàËÆ¶È:53.3% Tetrahedron 1999 55 9117-9132 New acorane- and cuparane-type sesqui- and new labdane- and seco-labdanne-type diterpenoids from the Japanese liverwort Jungermannia infusca (Mitt.) Steph. Fumihiro Nagashima, Makoto Suzuki, Shigeru Takaoka, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . (9R,9aS)-5,5,9-trimethyl-5,6,7,8,9,9a-hexahydro-1H-benzo[7]annulene-3-carbaldehyde ÏàËÆ¶È:53.3% Journal of Natural Products 2011 74 585-595 Male-Specific Sesquiterpenes from Phyllotreta Flea Beetles Robert J. Bartelt, Bruce W. Zilkowski, Allard A. Coss¨¦, Udo Schnupf, Karl Vermillion, and Frank A. Momany Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 2-{[(1R,2S,5R)-6,6-Dimethylbicyclo[3.1.1]heptyl-2]methylsulfonyl}-1H-benzimidazole C17H22N2O2S ÏàËÆ¶È:52.9% Chemistry of Natural Compounds 2012 48 38-42 SYNTHESIS OF NEW MONOTERPENE SULFONYLIMIDAZOLES M. Ya. Demakova,D. V. Sudarikov,S. A. Rubtsova,L. L. Frolova,and A. V. Kuchin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . (3R,6R)-6-(2-bromo-5-methoxymethoxy-4-methyl)phenyl-2-methylheptane-2,3-diol C17H27O4Br ÏàËÆ¶È:52.9% Heterocycles 2003 61 125-131 Enantiocontrolled Total Synthesis of (+)-Heliannuol D via Palladium-mediated Heterocyclization Hidetoshi Kishuku, Tomoyuki Yoshimura, Toshiyuki Kakehashi, Mitsuru Shindo, and Kozo Shishido* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . compound 12 ÏàËÆ¶È:52.9% Tetrahedron 1991 47 9411-9418 New examples of acyclic and cyclic C-15 acetogenins from laurencia pinnatifida. Reassignment of the absolute configuration for E and Z pinnatifidienyne. Manuel Noite, Antonio G. Gonzalez, Fernando Cataldo, Mat¨ªas L. Rodr¨ªguez, Ivan Brito Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 2-acetyl-3a¦Â-methyl-3a,6,7,7a¦Â-tetrahydro-1H-inden-4-oic acid methyl ester. C14H18O3 ÏàËÆ¶È:50% Journal of Natural Products 2007 70 241-245 Eremophilane-Type Sesquiterpene Derivatives from the Roots of Ligularia lapathifolia Dong-Qing Fei, Shi-Gang Li, Chun-Mei Liu, Gang Wu, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 20R-3¦Â-[(6-deoxy-¦Á-L-mannopyranosyl)oxy]-14¦Â-hydroxybufa-4-enolide C30H46O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1987 35 1839-1846 Studies on Cardiac Ingredients of Plants. III. Structural Confirmation and Biological Activity of Reduced Proscillaridins JUN MORI,SHIN-ICHI NAGAI,JINSAKU SAKAKIBARA,KAZUMI TAKEYA,YOSHIHIRO HOTTA and HIROAKI ANDO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . (5R,6S,9R)-6-Isopropyl-9-methyl-1-oxo-4-thiaspiro[4.5]-decane C12H22SO ÏàËÆ¶È:50% Chemistry of Natural Compounds 2008 44 728-731 OXIDATION OF MENTHONE OXOTHIOLANE A. V. Timshina, S. A. Rubtsova, I. N. Alekseev, M. I. Kodess,E. G. Mamochkina, P. A. Slepukhin, and A. V. Kuchin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . (4R,5R,6S,9R)-6-Isopropyl-9-methyl-1-oxo-4-thiaspiro[4.5]-decane-4-sulfoxide C12H22SO2 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2008 44 728-731 OXIDATION OF MENTHONE OXOTHIOLANE A. V. Timshina, S. A. Rubtsova, I. N. Alekseev, M. I. Kodess,E. G. Mamochkina, P. A. Slepukhin, and A. V. Kuchin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . Hexadeca-10E,12Z-dien-1-ol ÏàËÆ¶È:50% Chemistry of Natural Compounds 1993 29 668-673 INSECT PHEROMONES AND THEIR ANALOGUES XLVIII. A CONVENIENT SYNTHESIS OF THE 10E,12Z- AND 10E,12E- ISOMERS OF HEXADECADIEN-1-OL AND OF HEXADECA-10E,12Z-DIENAL -- COMPONENTS OF THE SEX PHEROMONE OF THE SILKWORM MOTH V. N. Odinokov, G. Yu. Ishmuratov, I. M. Ladenkova,O. V. Sokol'skaya, R. R. Muslukhov, V. R. Akhmetova,E. V. Gorobets, A. V. Kuchin, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . ¦Á¨C(2-Cyclopenten-1-yl)-4-methylbenzenemethanol C13H16O ÏàËÆ¶È:50% Molecules 2001 6 655-662 Use of Cyclic Allylic Bromides in the Zinc¨CMediated Aqueous Barbier¨CGrignard Reaction Gary W. Breton, John H. Shugart, Christine A. Hughey, Brian P. Conrad and Suzanne M. Perala Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 2¦Â−acetoxy-8¦Â,12-epoxy-13,14,15,16-tetranor-ent-labdan-17-ol ÏàËÆ¶È:50% Molecules 2007 12 2605-2620 Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II Luis E. Catal¨¢n, Karen C. Mar¨ªn, H¨¦ctor C. Altamirano, Mauricio C. Fritis and Mar¨ªa C. Chamy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . compoun 9 ÏàËÆ¶È:50% Natural Product Research 1993 2 129-135 Preparation of a Monochiral Terpenoid SynthonfFrom Carvone Using a Stereoselective Intramolecular Nitrile Oxide Cycloaddition J. -P. Gesson; S. A. M. Nieuwenhuis; B. Renoux Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . (2S,2aR,6S,7aS,7bS,8R,9S)-7b-butylhexahydro-9-methyl-4H-2,2,6-(epoxy[1]propanyl[3]ylidene)furo[2,3,4-gh]pyrrolizin-10-one C16H23NO6 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 935-941 Semisynthesis and Acetylcholinesterase Inhibitory Activity of Stemofoline Alkaloids and Analogues Kwankamol Sastraruji, Thanapat Sastraruji, Stephen G. Pyne, Alison T. Ung, Araya Jatisatienr and Wilford Lie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . pectinolide C C14H20O5 ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 583 Structure and Stereochemistry of Pectinolides A-C, Novel Antimicrobial and Cytotoxic 5,6-Dihydro-¦Á-pyrones from Hyptis pectinata Rogelio Pereda-Miranda, Lourdes Hern¨¢ndez, Manuela Judith Villavicencio, Miriam Novelo, Patricia Ibarra, Heebyung Chai, John M. Pezzuto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . 10,12-peroxycalamenene C15H20O2 ÏàËÆ¶È:50% Phytochemistry 1995 40 125-128 Antimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10, 12-Peroxycalamenene, a sesquiterpene endoperoxide C. Thebtaranonth, Y. Thebtaranonth, S. Wanauppathamkul, Y. Yuthavong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . Methyl omphalate ÏàËÆ¶È:50% Phytochemistry 1995 38 651-653 Sesquiterpenes and a phenolic compound from the liverwort Omphalanthus filiformis Motoo Tori, Katsuyuki Nakashima, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . methyl 4-(2-hydroxy-1,5-dimethyl-3-oxohexyl)-1-cyclo-hexene-1-carboxylate C16H26O4 ÏàËÆ¶È:50% Phytochemistry 1993 32 1163-1165 Juvabione analogues from two Abies sachalinensis trees Kenzo Kawai, Chika Takahashi, Tamie Takada, Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . 4,8,8-trimethyl-4-acetylcyclloctanon ÏàËÆ¶È:50% Helvetica Chimica Acta 1976 59 1-13 Die Thermolyse von 2,2,6,7-Tetramethyl-1,7-epidioxybicyclo[4.3.O]non-8-en von Werner Skorianetz und Gunther Ohloff Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . (1R,4R,4aS,8aS)-1,2,3,4,4a,7,8,8a-Octahydro-4-isopropyl-6-methylnaphthalen-1-ol C14H24O ÏàËÆ¶È:50% Organic Letters 2010 Vol.12,No.5 904-907 Total Synthesis of 10-Isocyano-4-cadinene and Determination of Its Absolute Configuration Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata,Erina Yoshimura, Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . (1R,4R,4aS,8aS)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol C14H24O ÏàËÆ¶È:50% The Journal of Organic Chemistry 2011 76 6558-6573 Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . 2,3,4,4a,5,6-hexahydro-7-methyl-pyrido[4,3-b]carbazole C16H18N2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2007 44 539-541 A short synthesis of the hexahydropyrido[4,3-b]carbazole core structure for the synthesis of aspidosperma alkaloids Yavuz Ergun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . 1-methyl-2-[1-(1,1-dimethylethyl)pentyl]-1H-imidazole C13H24N2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2004 41 335-341 Novel nucleophilic CC bond-forming tele-reaction of imidazole ring Shunsaku Ohta,Kentaro Sato,Ikuo Kawasaki,Yuko Yamaguchi,Satoko Nishio and Masayuki Yamashita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . compound 9d C18H21N ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2003 40 113-120 N-phenyl-substituted pyrrolidines,piperidines and azabicyclics by a tandem reduction-double reductive amination reaction Richard A. Bunce,Derrick M. Herron,Jason R. Lewis and Sharadsrikar V. Kotturi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . compound 3e C19H25NO2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2001 38 371-377 Inverse electron-demand 1,3-dipolar cycloaddition reactions of cyclooctyne with pyridinium bis(methoxycarbonyl)methylides Kiyoshi Matsumoto, Naoto Hayashi, Yukio Ikemi, Mitsuo Toda, Takane Uchida, Kinuyo Aoyama and Yoshihiro Miyakoshi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . methyl 2-[(1R,2R,6R)-6-isopropenyl-2-methoxy-3-methylcyclohex-3-enyl]-2-methyl-propionate C16H26O3 ÏàËÆ¶È:50% Indian Journal of Chemistry 2008 47B 1414-1422 Enantiospecific synthesis of (+)-trans-¦Á-himachalene via an intramolecular type II carbonyl ene reaction Srikrishna,A; Kumar,P Ravi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . (1R,7R,8R)-8-methoxy-6,6,9-trimethyl-2-methylenebicyclo[5.4.0]undec-9-en-4-ol C16H26O2 ÏàËÆ¶È:50% Indian Journal of Chemistry 2008 47B 1414-1422 Enantiospecific synthesis of (+)-trans-¦Á-himachalene via an intramolecular type II carbonyl ene reaction Srikrishna,A; Kumar,P Ravi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . 3-(9-(Julolidinyl)ethynyl)-6-methylpyridazine C19H19N3 ÏàËÆ¶È:50% Heterocycles 2010 81 1445-1457 Rod-Like Conjugated Molecules with Ethynylene Linkage and Pyridazines Moieties: Synthesis and Light Emitting Properties Caroline Hadad, Catherine Fiol-Petit, Anne-Sophie Cornec, Georges Dupas, Yvan Ramondenc, and Nelly Pl¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . lyconadin A ÏàËÆ¶È:50% Heterocycles 2009 77 679-729 The Lycopodium Alkaloids Yusuke Hirasawa, Jun'ichi Kobayashi, and Hiroshi Morita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . rac-cis-2-(2-methallyloxy)cyclohexanol C10H18O2 ÏàËÆ¶È:50% Heterocycles 2009 77 1123-1146 Synthesis of Annulated 1,4-Dioxanes and Perhydro-1,4-oxazines by Domino-Wacker-Carbonylation and Domino-Wacker-Mizoroki-Heck Reactions Lutz F. Tietze, Arne Heins, Mohammad Soleiman-Beigi, and Christian Raith Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 52 . 1-(2-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl)cyclohexan-1-ol C16H23NO ÏàËÆ¶È:50% Heterocycles 2004 63 401-409 Alkali Metal-mediated Synthesis of 1- and 4-Substituted N-Alkyl-1,2,3,4-tetrahydroisoquinolines Ugo Azzena,* Luisa Pisano, and Mario Pittalis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 53 . Compound 32 C15H20N2O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 1431-1443 Design, synthesis and preliminary pharmacological evaluation of new piperidine and piperazine derivatives as cognition-enhancers Elisabetta Martini, Carla Ghelardini, Silvia Dei, Luca Guandalini, Dina Manetti, Michele Melchiorre, Monica Norcini, Serena Scapecchi, Elisabetta Teodori, Maria Novella Romanelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 54 . 5-(3-Phenylpropyl)piperidin-2-one C14H19NO ÏàËÆ¶È:50% Helvetica Chimica Acta 2010 93 1180-1186 The Baylis¨CHillman Adducts as Valuable Source for One-Pot Multi-Step Synthesis: A Facile Synthesis of Substituted Piperidin-2-ones Deevi Basavaiah, Raju Jannapu Reddy and Dandamudi V. Lenin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 55 . Compound 5 cis ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2010 48 356-361 Relative acidities and structure analysis of cis and trans isomers of 1, 5-oxazaspiro[5.5] undecane derivatives by multinuclear magnetic resonance (pages 356¨C361) Jorge Antonio Guerrero-Álvarez, Wendy Paloma Mas-Ku, Cesar Garc¨ªas-Morales and Armando Ariza-Castolo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 56 . Compound 22 ÏàËÆ¶È:50% Magnetic Resonance in Chmesitry 2005 43 1057-1062 Complete 1H and 13C NMR spectral assignment of N-aralkylsulfonamides, N-sulfonyl-1, 2, 3, 4-tetrahydroisoquinolines and N-sulfonyl-2, 3, 4, 5-tetrahydro-1H-2-benzazepines. Conformational analysis of N-[((3', 4'-dichlorophenyl)methyl)sulfonyl]-3-methyl-2, Jorge L. Jios, Gustavo P. Romanelli, Juan Carlos Autino, H¨¦ctor E. Giaccio, Helmut Duddeck and Michael Wiebcke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 57 . Compound 2 ÏàËÆ¶È:50% Magnetic Resonance in Chmesitry 2002 40 659-665 Phenylselenenylmenthane derivatives and their enantiomeric discrimination by 1H and 13C NMR spectroscopy in the presence of a chiral dirhodium complex Shahid Malik, Stefan Moeller, Helmut Duddeck and Muhammad Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 58 . Faurinone ÏàËÆ¶È:50% Phytochemistry 1983 22 1505-1506 A structure of faurinone, a sesquiterpene ketone isolated from valeriana officinalis R. Bos, H. Hendriks, J. Kloosterman, G. Sipma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 59 . (R)-1-(1-Hydroxy-3-methylbutan-2-yl)-4-phenyl-1,2,5,6-tetrahydropyridine ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 2063-2068 Solid-phase Zincke route to pyridinium, tetrahydropyridine, and piperidine derivatives: vesamicol analogs Masahiro Eda, Mark J Kurth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 60 . (R)-4-(1,1-Dimethylethyl)-1-(1-hydroxy-3-phenylpropan-2-yl)-1,2,5,6-tetrahydropyridine ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 2063-2068 Solid-phase Zincke route to pyridinium, tetrahydropyridine, and piperidine derivatives: vesamicol analogs Masahiro Eda, Mark J Kurth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 61 . fragment A ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 6057-6060 Total synthesis of aspirin-triggered 15-epi-lipoxin A4 Ana R Rodrı́guez, Bernd W Spur Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 62 . compound 6e ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 607-609 Oxazoline azomethine imines preparation and cycloaddition with phenyl isocyanate Olivier Bedel, Dominique Urban, Yves Langlois Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 63 . compound 24 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 6975-6978 Towards a total synthesis of guanacastepene A: construction of fully functionalized AB and BC ring segments Goverdhan Mehta, Jayant D Umarye, Vanessa Gagliardini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 64 . compound 22 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 8149-8151 Homocoupling of alkyl-, alkenyl-, and arylboronic acids J.R. Falck, Suchismita Mohapatra, Muralidhar Bondlela, Sylesh K. Venkataraman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 65 . compound 10b C16H22S ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 9615-9619 Thermal rearrangements of bis-allenyl thiosulfonates. Synthesis of novel thienothiophene and thieno-oxathiine derivatives Mihail L. Birsa, Marina Cherkinsky, Samuel Braverman Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 66 . compound cis-3a ÏàËÆ¶È:50% Tetrahedron Letters 2003 44 6809-6812 Clean and atom-economic synthesis of octahydroacridines: application to essential oil of citronella Raquel G Jacob, Gelson Perin, Giancarlo V Botteselle, Eder J Lenardão Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 67 . compound 2e ÏàËÆ¶È:50% Tetrahedron Letters 2003 44 9169-9171 A simple and fast procedure for efficient synthesis of ¦Â- and ¦Ã-azidoarylketones Pradeep N.D. Singh, Sivaramakrishnan Muthukrishnan, Rajesh S. Murthy, Rodney F. Klima, Sarah M. Mandel, Michael Hawk, Nina Yarbrough, Anna D. Gudmundsd¨®ttir Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 68 . compound 7 C16H25N ÏàËÆ¶È:50% Tetrahedron Letters 2004 45 3565-3568 Stereoselective synthesis of activated cyclopropanes with an ¦Á-pyridinium acetamide bearing an 8-phenylmenthyl group as the chiral auxiliary Satoshi Kojima, Kyoko Hiroike, Katsuo Ohkata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 69 . compound 19 C16H26O3 ÏàËÆ¶È:50% Tetrahedron Letters 2004 45 6867-6870 Enantiospecific first total synthesis of (+)-trans-¦Á-himachalene A. Srikrishna, P. Ravi Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 70 . compound 24 C16H26O2 ÏàËÆ¶È:50% Tetrahedron Letters 2004 45 6867-6870 Enantiospecific first total synthesis of (+)-trans-¦Á-himachalene A. Srikrishna, P. Ravi Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 71 . compound 2b ÏàËÆ¶È:50% Tetrahedron Letters 2004 45 6733-6736 Access to novel substituted diazaadamantanes via semi-natural tetrahydrocytisine Alexandre V. Ivachtchenko, Alexandre Khvat, Sergey E. Tkachenko, Yuri B. Sandulenko, Vladimir Y. Vvedensky Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 72 . 5-Fluoro-1,2,3,4-tetrahydroacridine C13H12FN ÏàËÆ¶È:50% Tetrahedron Letters 2005 46 767-770 Synthesis of regiospecifically substituted quinolines from anilines Giorgio Chelucci, Ilaria Manca, Gerard A. Pinna Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 73 . compound 3a ÏàËÆ¶È:50% Tetrahedron Letters 2005 46 1039-1044 Ionic liquid accelerated intramolecular hetero-Diels-Alder reactions: a protocol for the synthesis of octahydroacridines J.S. Yadav, B.V.S. Reddy, Lakshindra Chetia, G. Srinivasulu, A.C. Kunwar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 74 . ÃÀàËûຠÏàËÆ¶È:50% Chinese Journal of Medicinal Chemistry 2007 17 314-315 Liposoluble constituents of Dracocephalum tanguticum Maxim. (I) ZHENG Hong-ting, ZHANG Guo-gang, ZHENG Ya-fu, JIN Yin-ping, DU Shu-shan, DENG Zhi-wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 75 . compound 13 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1994 2 1423-1434 Structure¡ªactivity studies leading to potent chloride channel blockers: 5e-tert-butyl-2-[4-(substituted-ethynyl)phenyl]-1,3-dithianes Qing X. Li, John E. Casida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 76 . 1-Phthalimido-7-[[N-ethyl-N-[(2-mesitylene) sulfonyl]-amino]-4-azaheptane ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1996 4 825-836 Synthesis and evaluation of a polyamine phosphinate and phosphonamidate as transition-state analogue inhibitors of spermidine/spermine-N1-acetyltransferase Ronghui Wu, Nada H. Saab, Huatao Huang, Laurie Wiest, Anthony E. Pegg, Robert A. Casero Jr, Patrick M. Woster Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 77 . 9-Methoxycarbonylnonyltriphenylphosphonium bromide ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1997 5 1267-1274 Identification and biosynthesis of (E,E)-10,12-tetradecadienyl acetate in Spodoptera littoralis female sex pheromone gland Isabel Navarro, Esther Mas, Gemma Fabri¨¤s, Francisco Camps Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 78 . 7-[4-Hydroxybutyl]-1,2,3,4-tetrahydronaphthalene-1-one C14H18O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1998 6 2421-2439 The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewisx Paul V. Murphy, Rod E. Hubbard, David T. Manallack, Ruth E. Wills, John G. Montana, Richard J.K. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 79 . 7-Carboxypropyl-1,2,3,4-tetrahydronaphthalene-1-one C14H16O3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1998 6 2421-2439 The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewisx Paul V. Murphy, Rod E. Hubbard, David T. Manallack, Ruth E. Wills, John G. Montana, Richard J.K. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 80 . 6-Carboxypropyl-1,2,3,4-tetrahydronaphthalene C14H18O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1998 6 2421-2439 The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewisx Paul V. Murphy, Rod E. Hubbard, David T. Manallack, Ruth E. Wills, John G. Montana, Richard J.K. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 81 . (2S,2aR,6S,7aS,7bS,8R,9S)-7b-(1-Butenyl)hexahydro-9-methyl-4H-2,2,6-(epoxy[1]propanyl[3]ylidene)furo[2,3,4-gh]pyrrolizin-10-one C16H21NO3 ÏàËÆ¶È:50% Tetrahedron 2012 68 598-602 Oxidation of acyclic alkenes and allyl and benzyl ethers with DIB/t-BuOOH/Mg(OAc)2 Thanapat Sastraruji, Stephen G. Pyne, Alison T. Ung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 82 . 1-Nitro-N-tosylnonan-2-amine C16H26N2O4S ÏàËÆ¶È:50% Tetrahedron 2012 68 1736-1744 The use of samarium or sodium iodide salts as an alternative for the aza-Henry reaction Humberto Rodr¨ªguez-Solla, Carmen Concell¨®n, Noem¨ª Alvaredo, Raquel G. Soengas Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 83 . (20R)-24-Methylenecholestane-3¦Â,21-diol ÏàËÆ¶È:50% Journal of the Chemical Society, Perkin Transactions 1 1984 2277-2282 Steroids from the starfish Euretaster insignis: a novel group of sulphated 3¦Â,21-dihydroxysteroids Maria V. D'Auria, Ester Finamore, Luigi Minale, Cosimo Pizza, Raffaele Riccio, Franco Zollo, Michelle Pusset and Philippe Tirard Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 84 . compound 1bc C21H30N4O4F6 ÏàËÆ¶È:50% Heterocycles 2000 53 1317-1328 Solution Parallel Synthesis of Cyclic Guanidines Christelle Marmillon, Jacques Bompart, Mich¨¨le Calas, Roger Escale,* and Pierre-Antoine Bonnet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 85 . (1S,5R)-6-isopropylidine-1,5-dimethylbicyclo-[3.3.0]octan-3-one C13H20O ÏàËÆ¶È:50% Indian Journal of Chemistry 2011 50B 1092-1106 Enantiospecific first total synthesis of cucumin-H Srikrishna, A; Dethe, Dattatraya H Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 86 . methyl 2,6-dimethyl-10-oxoundeca-(2E,6Z)-dienoate ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2005 41 1228-1229 ChemicallyRationalApproachtotheSynthesisofPrecursorsofthe¡°Prenyl¡±FragmentinEpothilones F.A. Gimalova, Z.A. Yusupov, T.A. Maslova and M.S. Miftakhov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 87 . 5-exo-acetoxy-2,2,3-exotrimethylbicyclo[2.2.1]-heptane C12H20O2 ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2001 37 1418-1429 Reactions of Some Terpenes and Their Derivatives with Acylating Agents in the Presence of Aluminosilicate Catalysts K. P. Volcho, L. E. Tatarova, E. V. Suslov, D. V. Korchagina and N. F. Salakhutdinov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 88 . compound 2 ÏàËÆ¶È:50% Organic Magnetic Resonance 1983 21 122-124 Differentiation of diastereomeric bornane derivatives by 13C NMR spectroscopy Helmut Duddeck, Blagoy Blagoev, Nikolina D. Berova and Vassil Vassilev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 89 . compound 1 ÏàËÆ¶È:50% Organic Magnetic Resonance 1982 19 95-97 The assignment of 13C NMR shift data in clerodanes and related structures J. M. Luteijn, A. Van Veldhuizen and A. De Groot Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 90 . N-tert-Butoxycarbonyl-5-(hexylthiomethyl)pyrrolidin-2-one C16H29NO3S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 5500-5506 Substituted lactam and cyclic azahemiacetals modulate Pseudomonas aeruginosa quorum sensing Venkata L.A. Malladi, Adam J. Sobczak, Natalie Maricic, Senthil Kumar Murugapiran, Lisa Schneper, John Makemson, Kalai Mathee, Stanislaw F. Wnuk Structure 13C NMR ̼Æ×Ä£Äâͼ |
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