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²éѯ½á¹û£º¹²²éµ½506¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1(10)-en-2-oxo-7¦Á-isopropanoleremophilane C15H24O2 ÏàËÆ¶È:93.3% Chemical Research in Chinese Universities 2009 25 480-482 Two Eremophilane-type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana(Hemsl.) Greenm WANG Cai-fang, ZHAO Yu, LIU Yan-ze and ZHANG Zhen-zhong Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (rel)-4¦Â,5¦Â,7¦Â-eremophil-1(10)-en-2-oxo-12-oic acid ÏàËÆ¶È:80% Qu¨ªmica Nova 2013 36 1008-1013 SESQUITERPENOS DE Ocotea lancifolia (Lauraceae) Maria Jos¨¦ de Camargo, Mayker Lazaro Dantas Miranda, Camila Miyuki Kagamida, Edilene Delphino Rodrigues, Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . viridiflorol C15H26O ÏàËÆ¶È:66.6% Acta Botanica Boreali-Occidentalia Sinica 2006 26 2146-2149 Liposoluble Constituents in Eucalyptus globulus Labill. Fruits TAN MAN-Liang, WANG Ye, ZHOU Li-gang, JIANG Wei-bo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5¦Á-hydroxyisopterocarpolone C15H24O3 ÏàËÆ¶È:66.6% Phytochemistry 1996 43 815-817 Eudesmane sesquiterpenes from Artemisia eriopoda Jin-Feng Hu, Su-Ping Bai, Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 7-epiglobulol C15H26O2 ÏàËÆ¶È:66.6% Phytochemistry 1994 37 1023-1025 The hydroxylation of globulol and 7-epiglobulol by Cephalosporium aphidicola James R. Hanson, Peter B. Hitchcock, Revathy Manickavasagar Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (+)-5¦Á-Hydroxy-isop terocarpo lone ÏàËÆ¶È:66.6% Chemical Journal of Chinese Universities 2005 26 1281-1283 Total Syn thes is of 5¦Á-Hydroxy-isopterocarpolone GUAN Yu-Kun,LI Ping,ZHOU Gang,GAO Xiao-Lei,LI Yu-Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4-epi-globulol C15H26O ÏàËÆ¶È:66.6% Journal of the Brazilian Chemical Society 1990 1 105-109 Composition of the Essential Oil of Vassoura. Carmen Lucia Queiroga, Alberto Fukai and Anita J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (-)-10-epi-Globulol ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 1995 1995 1039-1043 New sesquiterpene ethers and other constituents isolated from Brazilian vassoura oil Peter Weyerstahl, Christian Christiansen and Helga Marschall Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . norlongilactone ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2012 37 1973-1976 Sesquiterpenes and monoterpene from Aquilaria sinensis YANG Lin; QIAO Lirui; XIE Dan; DAI Jungui; GUO Shunxing Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . methyl 3-oxoartemisinate structure C16H22O3 ÏàËÆ¶È:62.5% Planta Medica 1996 62 359-360 Production of Methyl 3-Oxoartemisinate from Methyl Artemisinate by Suspension Cell Culture of Mentha piperita Soo-Un Kim and Hyung-Jin Kwon Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (7¦Á,9¦Á,10¦Á)-9,10-epoxy-eremophilan-11-ol C15H26O2 ÏàËÆ¶È:60% Helvetica Chimica Acta 2008 Vol. 91 1712 Two New Eremophilane-Type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana (Hemsl.) Greenm Cai-FangWang, Yu Zhao, Yan-Ze Liu, and Zhen-Zhong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . rhombidiol C15H26O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2005 53(2) 238-240 Eudesmane Sesquiterpenes from the Aquatic Fungus Beltrania rhombica Vatcharin RUKACHAISIRIKUL, Chutanat KAEWBUMRUNG,Souwalak PHONGPAICHIT,and Zubaidah HAJIWANGOH Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . cadinane-4¦Â,5¦Á,10¦Â-triol C15H28O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . muurolane-4¦Â,5¦Â,10¦Â-triol C15H28O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (-)1¦Â,4¦Â,6¦Átrihydroxy-eudesmane C15H28O3 ÏàËÆ¶È:60% Phytochemistry 2008 69 2367-2373 Sesquiterpenoids from Homalomena occulta affect osteoblast proliferation,differentiation and mineralization in vitro Yong-Mei Hu, Chuan Liu, Ka-Wing Cheng, Herman H.-Y. Sung, Lan D. Williams,Zhong-Lin Yang Wen-Cai Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (()-3,7,11-trimethyl-10-dodecen-1,7-diol ÏàËÆ¶È:60% Journal of Natural Products 2002 65 1319-1322 African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (4Z,8¦Á,11S)-caryophyll-4(5)-ene-8,14-diol C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 2000 63 44-47 Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 10¦Á-hydroxyamorphan-4-en-3-one C15H24O2 ÏàËÆ¶È:60% Journal of Natural Products 1997 60 38-40 Bioactive Compounds from Taiwania cryptomerioides Kan He, Lu Zeng, Guoen Shi, Geng-Xian Zhao, John F. Kozlowski, and Jerry L. McLaughlin Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . zingiberene-3,6-¦Á-endoperoxide C15H24O2 ÏàËÆ¶È:60% Planta Medica 1996 62 565-566 Sesquiterpene Peroxides from Senecio selloi and Eupatorium rufescens G. R¨¹cker, E. P. Scherikel, D. Manns, R. Mayer,K. Heiden, and B. M. Heinzmann Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 4¦Â,5¦Á, 10¦Â-trihydroxycadinane C15H26O2 ÏàËÆ¶È:60% Planta Medica 1997 63 250-254 Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti) Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Pterodontic acid C15H22O2 ÏàËÆ¶È:60% Acta Botanica Yunnanica 1996 18£¨3£© 349-352 FOUR NEW SESQUITERPENOIDS FROM LAGGERA PTERODONTA LI Shun-Lin, DING Jing-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (2RS,4RS,6SR)-2-Cyclohexyltetrahydro-6-(2-methylprop-1-en-1-yl)-2H-pyran-4-ol C15H26O2 ÏàËÆ¶È:60% Helvetica Chimica Acta 2009 92 1333-1340 Alkyl-Group Selection in an Acidic-Surfactant-Promoted Reaction of Homoallyl Alcohols and Aldehydes in Water Takanori Hatakeyama, Yuki Chisaka, Chiaki Kuroda Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . laggerone B ÏàËÆ¶È:60% Chinese Chemical Letters 1996 7 1093-1094 EUDESMANES AND EUDESMANOIC GLUCOSIDES FROM LAGGERA PETERODONTA YU ZHAO,JIAN MIN YUE,JING KAI DING,ZHONG WEN LIN AND HAN DONG SUN Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (-)-10¦Â-hydroxy-4-muurolen-3-one C C15H24O2 ÏàËÆ¶È:60% Chinese Chemical Letters 2008 19 1265-1267 First total synthesis of 10¦Á-hydroxy-4-muurolen-3-one and its C10-isomer Fu Qiang Bi, Li Jing Fang, Chen Xi Zhang, Yu Lin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . valerianol ÏàËÆ¶È:60% Phytochemistry 1999 52 1063-1067 The hydroxylation of the sesquiterpenoid valerianol by Mucor plumbeus Simone Fontes Arantes, James R. Hanson, Peter B. Hitchcock Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 1,4-epidioxy-bisabola-2,10-diene(1S,4R,6R) C15H24O ÏàËÆ¶È:60% Phytochemistry 1997 45 537-544 Oxygenated bisabolanes from Alpinia densibracteata Lai-King Sy, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 5¦Á,11-dihydroxy-3-ene-dudesman-2-one C15H24O3 ÏàËÆ¶È:60% Phytochemistry 1997 44 459-464 Eudesmane sesquiterpenes from Laggera pterodonta Yu Zhao, Jianmin Yue, Zhongwen Lin, Jingkai Ding, Handong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (¡À)-[1S-(1¦Â,4¦Â,4a¦Â,6¦Â,8a¦Á]-7-Chloro-1,6-di-methyl-4-(1-methylethyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-l,6-naphthalenediol ÏàËÆ¶È:60% 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 29 . 6-isocedrol ÏàËÆ¶È:60% Journal of Natural Products 1984 Vol 47 924-933 13C-nmr Study of Cedrol, 6-Isocedrol, and ¦Á-Cedrene P. Joseph-Nathan, R. L. Santillan, A. Guti¨¦rrez Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 6-isocedrol ÏàËÆ¶È:60% Journal of Natural Products 1986 Vol 49 79 13C-nmr Studies of Cedranolides P. Joseph-Nathan, A. Guti¨¦rrez, J. D. Hern¨¢ndez, L. U. Rom¨¢n, R. L. Santillan Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 8-Epicedrol ÏàËÆ¶È:60% Phytochemistry 1995 39 1081-1084 The biotransformation of 8-epicedrol and some relatives by Cephalosporium aphidicola Estelle Gand, James R. Hanson, Habib Nasir Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . ent-halima-5(10),13-dien-16,15-olide C20H30O2 ÏàËÆ¶È:60% Phytochemistry 1995 38 189-194 Clerodane and ent-halimane diterpenes from polyalthia longifolia Noriyuki Hara, Hitomi Asaki, Yoshinori Fujimoto, Yogesh Kumar Gupta, Ashish Kumar Singh, Mahendra Sahai Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 3-oxofabiaimbricatan C15H24O2 ÏàËÆ¶È:60% Phytochemistry 1994 36 1439-1442 Sesquiterpenes from Fabiana imbricata Guillermo Schmeda-Hirschmann, Fani Papastergiou Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . (+)-cis-14-Normuurol-5-en-4-one ÏàËÆ¶È:60% Phytochemistry 1994 36 961-965 cis-calamenene-related sesquiterpenoids from Cupressus bakeri foliage Kim Young-Kyoon, Laurence G. Cool, Eugene Zavarin Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . compound 12 ÏàËÆ¶È:60% Phytochemistry 1994 37 1101-1107 Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species J.Alberto Marco, Juan F. Sanz-Cervera, Vicente Garcia-Lliso, Alfonso Susanna, Nuria Garcia-Jacas Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . compound 2 ÏàËÆ¶È:60% Tetrahedron Letters 2000 41 9219-9222 Synthesis and reactions of a novel chlorostannane resin: coupling with functionalized organozinc halides Xizhen Zhu, Bruce E. Blough, F. Ivy Carroll Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . ¦Á-Humulen-14-oic acid ÏàËÆ¶È:60% Phytochemistry 1982 21 685-689 ¦Á-Humulene derivatives including a sesquiterpene acid with a rearranged carbon skeleton from Lychophorora columnaris Ferdinand Bohlmann, Christa Zdero, Harold Robinson, Robert M. King Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . compound 2 ÏàËÆ¶È:60% Pharmazie 2002 57 59-61 Microbiological conversion of a - and -eudesmol mixture by Rhizopus G.T. Maatooq - J.J. Hoffmann Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 1S,4R,6R-1,4-endoperoxy-bisabola-2,10-diene ÏàËÆ¶È:60% Archives of Pharmacal Research 2000 23 151-154 Cytotoxic peroxides from Artemisia stolonifera Hak Cheol Kwon, Sang Un Choi and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 5(10),13E-ent-halimadien-15,16-olide C20H30O2 ÏàËÆ¶È:60% Tetrahedron Letters 2003 44 369-372 Synthesis and absolute configuration of three natural ent-halimanolides with biological activity I.S Marcos, A.B Pedrero, M.J Sexmero, D Diez, P Basabe, F.A Hern¨¢ndez, J.G Urones Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . (1R,7S,10S)-7-(1-Methylethyl)-10-methylbicyclo[4.4.0]dec-5-en-4-one ÏàËÆ¶È:60% Journal of the Chemical Society, Perkin Transactions 1 2000 189-194 Synthesis of sesquiterpene allylic alcohols and sesquiterpene dienes from Cupressus bakeri and Chamaecyparis obtusa Koon-Sin Ngo and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . compound 3a C14H24O2 ÏàËÆ¶È:60% Tetrahedron 2002 58 1647-1656 Studies on the synthesis of (¡À)-pathylactone A, a nor-sesquiterpene lactone isolated from marine sources Fernando Coelho, Gaspar Diaz Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 4-keto-15-nor-muurol-5-ene C14H22O ÏàËÆ¶È:60% Tetrahedron 1999 55 15109-15126 Autoxidation of 4-amorphen-11-ol and the biogenesis of nor- and seco-amorphane sesquiterpenes from fabiana imbricata Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . exo,exo-8-methyltetracyclo[4.4.(12,5).(17,10).0(1,6)]-dodec-exo-3(4)-yl acetate C15H22O2 ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2005 41 974-977 Synthesis of Esters from Cage-Like Unsaturated Hydrocarbons, Carboxylic Acid Anhydrides, and Water M. K. Mamedov, E. K. Nabieva and R. A. Rasulova Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . ¦Ã-eudesmol ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung C 2002 57 654-659 Microbial Transformation of a b- and g-Eudesmols Mixture G. T. Maatooq Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . (-)-nor-aromadendr-10¦Â-ol ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung C 2009 64 840-846 Structure-Activity Relationships of Aromadendranes in Uterus-Relaxant Activity N. P¨¦rez-Hern¨¢ndez, H. Ponce-Monter, M. I. Ortiz, R. Cariño-Cort¨¦sa, and P. Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . compound 9 ÏàËÆ¶È:60% Canadian Journal of Chemistry 1986 64 1-4 Stress metabolites of Solanummelongena: biosynthetic studies and isolation of auberganol and ¦Á- and ¦Â-eudesmol Albert Stoessl, J.B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . costic acid ÏàËÆ¶È:60% Phytochemistry 2013 95 19-93 Sesquiterpenoids in subtribe Centaureinae (Cass.) Dumort (tribe Cardueae, Asteraceae): Distribution, 13C NMR spectral data and biological properties Review Article Maurizio Bruno, Svetlana Bancheva, Sergio Rosselli, Antonella Maggio Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . Isolongifolene Alcohol ÏàËÆ¶È:60% Journal of Agricultural and Food Chemistry 1994 42 138-142 Structure elucidation of oxidation-reduction products of isolongifolene Isabelle Bombarda, Jacqueline Smadja, Emile M. Gaydou, Jacques Yves Conan, Robert Faure Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . (-)-epi-cedrol C15H26O ÏàËÆ¶È:60% Journal of Agricultural and Food Chemistry 2012 60 124-128 Phytochemicals from Cunninghamia konishii Hayata Act as Antifungal Agents Sen-Sung Cheng, Min-Jay Chung, Chun-Ya Lin, Ya-Nan Wang, and Shang-Tzen Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . (6S,7R)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one ÏàËÆ¶È:60% European Journal of Organic Chemistry 1998 1998 2851-2854 Synthesis of (6S,7S)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the Opposite Enantiomer of the Antibacterial Sesquiterpene from Premnaoligotricha, and the (R) Enantiomer of Ancistrodial, the Defensive Sesquiterpene from Ancistrotermes cavithorax Sayo Horiuchi, Hirosato Takikawa and Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . (6R*,7S *)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one C15H26O2 ÏàËÆ¶È:60% European Journal of Organic Chemistry 1996 1996 891-897 Synthesis of Mono- and Sesquiterpenoids, XXV. Synthesis of (6R*,7R*)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the Racemate of the Antibacterial Sesquiterpene from Premna oligotricha, and Its (6R*,7S*) Isomer Arata Yajima, Hirosato Takikawa and Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . 14-chloroxeniaphylla-4,8(19)-dien-15-ol C20H33ClO ÏàËÆ¶È:60% Australian Journal of Chemistry 1981 34 2657-2664 Studies of Australian soft corals. XXV. Several caryophyllene-based diterpenes from a Nephthea species A Ahond, BF Bowden, JC Coll, J Fourneron and SJ Mitchell Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . 5,10-dehydroambliol B ÏàËÆ¶È:60% The Journal of Organic Chemistry 1988 53 4574-4578 Sesterterpene sulfates from a sponge of the family Halichondriidae Michael R. Kernan, D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . ¦Ã-Eudesmol ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 1995 33 233-235 Two-dimensional NMR of sesquiterpenes. 8¡ªcomplete assignment of 1H and 13C NMR spectra of seven sequiterpene alcohols from Neocallitropsis pancheri Phila Raharivelomanana, Jean-Pierre Bianchini, Aim¨¦ Cambon, Marcel Azzaro and Robert Faure Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . (6¦Á,8¦Á)-6-acetyloxy)eremophil- 7(11)-en-12,8-olide C17H24O4 ÏàËÆ¶È:58.8% Helvetica Chimica Acta 2006 Vol. 89 915 Terpenoids from the Roots of Ligularia muliensis Qiu-Hong Wu, Chun-Mei Liu, Yan-Jun Chen, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . compound 11 C21H28O4 ÏàËÆ¶È:58.8% Journal of Natural Products 2003 66 1263-1265 Determination of the Absolute Stereochemistry of Cyclosmenospongine Natalia K.Utkina,Vladimir A. Denisenko, Olga V. Scholokova, and Aleksandra E. Makarchenko Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . (2R,3R)-2-Hydroxy-3-(hydroxymethyl)-3,5-dimethyl-N-(3-oxo-3-(pentylamino)propyl)hexanamide C17H34N2O4 ÏàËÆ¶È:58.8% 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 59 . nardosinanol D C16H26O4 ÏàËÆ¶È:56.2% Journal of Natural Products 2008 71(3) 375-380 Nardosinanols A#I and Lemnafricanol, Sesquiterpenes from Several Soft Corals, Lemnalia sp., Paralemnalia clavata, Lemnalia africana, and Rhytisma fulvum fulvum Ashgan Bishara, Dina Yeffet, Mor Sisso, Guy Shmul, Michael Schleyer, Yehuda Benayahu, Amira Rudi, and Yoel Kashman Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . 3¦Á,4¦Á-Isopropyliden-¦Â-ionol C16H26O3 ÏàËÆ¶È:56.2% Journal of Asian Natural Products Research 2005 7 151-156 Three new compounds from Isodon melissoides AI-HUA ZHAO, RONG-TAO LI, BEI JIANG, JI-XIA ZHANG,QIN-SHI ZHAO and HAN-DONG SUN Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . 1-naphthalene acetic-7-oxo-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a,5-tetramethyl acid C16H24O3 ÏàËÆ¶È:56.2% Phytochemistry 1992 31 1823-1825 Tetranorditerpenes from Detarium microcarpum Rita Aquino, Maria Letizia Ciavatta, Nunziatina De Tommasi, Eszter G¨¤cs-Baitz Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . norambreinolide-18,6¦Á-olide C16H22O4 ÏàËÆ¶È:56.2% Journal of Natural Products 2010 73 1601-1605 Sesterterpenoids and Other Constituents of Salvia sahendica Firouz Matloubi Moghaddam, Mahdi Moridi Farimani, Marjan Seirafi, Salman Taheri, Hamid Reza Khavasi, Jandirk Sendker, Peter Proksch, Victor Wray, and RuAngelie Edrada Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . flavalin E C16H24O3 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2011 59(6) 698-702 Sesquiterpenoids from the Formosan Soft Coral Lemnalia flava Jui-Hsin SU, Yi LU, Wen-Yu HUNG,Chiung-Yao HUANG, Michael Y. CHIANG,Ping-Jyun SUNG, Yao-Haur KUO,and Jyh-Horng SHEU Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . paralemnolin P C16H24O3 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2010 58 30-33 Paralemnolins J¡ªP, New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoide Guey-Horng Wang, Ho-Cheng Huang, Jui-Hsin Su, Yang-Chang Wu and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . 1¦Â-t-butoxy-4-(3'-oxobutyl)-7a¦Â-methyl-7,7a-dihydro-5(6H)-indanone ÏàËÆ¶È:56.2% Steroids 1984 44 283-292 [1,2,3,4-13C] Testosterone and [1,2,3,4-13C] estradiol Gijsbert Zomer, Hans Wynberg, Nick M. Drayer Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . compound 11a ÏàËÆ¶È:56.2% Tetrahedron Letters 2004 45 6017-6020 A new approach to the synthesis of polycyclic structures Michael E Briggs, Myriem El Qacemi, Chakib Kalaı̈, Samir Z Zard Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . DL-N-[5-(p-Amidinophenyl)pentanoyl]-3-methyl-¦Â-alanineethylester C18H27N3O3 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 1995 3 539-551 A novel series of orally active antiplatelet agents Jeffery A. Zablocki, Foe S. Tjoeng, Philippe R. Bovy, Masateru Miyano, Robert B. Garland, Kenneth Williams, Lori Schretzman, Mark E. Zupec, Joseph G. Rico, Richard J. Lindmark, Mihaly V. Toth, Dudley E. McMackins, Steven P. Adams, Susan G. Panzer-Knodle, Structure 13C NMR ̼Æ×Ä£Äâͼ 68 . [15-(13)C2H3]-E-7,11-Dehydro-dihydroartemisinic acid methyl ester C16H24O2 ÏàËÆ¶È:56.2% Tetrahedron 2007 63 9548-9566 In vivo transformations of artemisinic acid in Artemisia annua plants Geoffrey D. Brown, Lai-King Sy Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . tessaric acid methyl esthe[rmethyl 2-((2R,8S,8aR)-8,8a-dimethyl-6-oxo-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl)acrylate] C16H24O2 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2009 17 6251-6256 Tessaric acid derivatives induce G2/M cell cycle arrest in human solid tumor cell lines Leticia G. Le¨®n, Osvaldo J. Donadel, Carlos E. Tonn, Jos¨¦ M. Padr¨®n Structure 13C NMR ̼Æ×Ä£Äâͼ 70 . (3a'S,4'R,6a'R)-5,5-dimethyl-4'-(3-methylbut-2-enyl)-tetrahydro-1'H-spiro[[1,3]dioxane-2,2'-pentalen]-5'(3'H)-one C18H28O3 ÏàËÆ¶È:56.2% European Journal of Organic Chemistry 2010 1149-1157 Synthesis of Functionalized Hydropentalenes by an Asymmetric Deprotonation/Alkylation Strategy Vanessa Lutz, Angelika Baro, Peter Fischer and Sabine Laschat Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . 13,19-dihydroxy-halima-5(10),14-diene C20H34O2 ÏàËÆ¶È:55.5% Biochemical Systematics and Ecology 2004 32 45-53 Diterpenes from Stevia gilliesii Tamara L. Meragelman, Diego S. Pedrosa, Roberto R. Gil Structure 13C NMR ̼Æ×Ä£Äâͼ 72 . 19-nortestosterone ÏàËÆ¶È:55.5% Steroids 2005 70 193-198 Steroids¡¯ transformations in Penicillium notatum culture Agnieszka Bartma¨½ska, Jadwiga Dmochowska-Gładysz, Ewa Huszcza Structure 13C NMR ̼Æ×Ä£Äâͼ 73 . Solajiangxin E C18H28O3 ÏàËÆ¶È:55.5% Phytochemistry Letters 2013 6 453-456 Three new cytotoxic sesquiterpenoids from Solanum lyratum Fang Yao, Qin-Lan Song, Lei Zhang, Gui-Sheng Li, Sheng-Jun Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 74 . 2-Hydroxysolajiangxin E C18H28O4 ÏàËÆ¶È:55.5% Phytochemistry Letters 2013 6 453-456 Three new cytotoxic sesquiterpenoids from Solanum lyratum Fang Yao, Qin-Lan Song, Lei Zhang, Gui-Sheng Li, Sheng-Jun Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 75 . (-)-Perhydro-3¦Á,4a¦Á,7,7,10a¦Â-pentamethyl-cis-4a-transoid-10a,10b-trans-6a-naphtho[2,1-b]pyran ÏàËÆ¶È:55.5% Helvetica Chimica Acta 1986 69 163-173 Conformation-Odor Relationships in Norlabdane Oxides G¨¹nther Ohloff, Christian Vial, Edouard Demole, Paul Enggist, Wolfgang Giersch, Elise J¨¦gou, Andrew J. Caruso, Judith Polonsky and Edgar Lederer Structure 13C NMR ̼Æ×Ä£Äâͼ 76 . manaarenolide F C20H32O6 ÏàËÆ¶È:55% Journal of Natural Products 2006 69(8) 1134-1139 Manaarenolides A−I, Diterpenoids from the Soft Coral Sinularia manaarensis Jui-Hsin Su, Atallah F. Ahmed, Ping-Jyun Sung, Chih-Hua Chao, Yao-Haur Kuo, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 77 . (6¦Â)-5(R)-[2-(3-Furanyl)ethyl]-1,1,5,6-tetramethyl-1,2,3,4,5,6,7,8-octahydronaphthalene C20H30O ÏàËÆ¶È:55% Journal of Natural Products 2000 63 1623-1625 Synthesis of 16,18-Dihydroxycleroda-3,13Z-dien-16,15-olide,(+)-16-Hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-Hydroxyhalima-5(10),13-dien-16,15-olide from (+)-Hardwickiic Acid Paulo M. Imamura, and Marta Costa Structure 13C NMR ̼Æ×Ä£Äâͼ 78 . Sapinsignoid E C20H34O3 ÏàËÆ¶È:55% Journal of Natural Products 2012 75 722-727 Cytotoxic Diterpenoids from Sapium insigne Hong-Bing Liu, Hua Zhang, Jin-Hai Yu, Cheng-Hui Xu, Jian Ding, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 79 . mixture of 2-bromo-2c-isobutyryl-3,3-dimethylcyclopropyl-1r-methanol and 1-bromo-2-isopropyl-6,6-dimethyl-3-oxabicyclo[3.1.0]hexan-2-ol C10H18BrO2 ÏàËÆ¶È:55% Russian Journal of Organic Chemistry 2005 41 1601-1609 Synthesis of 1-Bromosubstituted Analogs of cis-Deltamethrinic and cis-Permethrinic Acids A. E. Sheshenev, M. S. Baird and I. G. Bolesov Structure 13C NMR ̼Æ×Ä£Äâͼ 80 . 15-chloroxeniaphylla-4,8(19)-dien-14-ol C20H33ClO ÏàËÆ¶È:55% Australian Journal of Chemistry 1981 34 2657-2664 Studies of Australian soft corals. XXV. Several caryophyllene-based diterpenes from a Nephthea species A Ahond, BF Bowden, JC Coll, J Fourneron and SJ Mitchell Structure 13C NMR ̼Æ×Ä£Äâͼ 81 . xeniaphylla-4,8(19)-diene-14,15-diol C20H34O2 ÏàËÆ¶È:55% Australian Journal of Chemistry 1981 34 2657-2664 Studies of Australian soft corals. XXV. Several caryophyllene-based diterpenes from a Nephthea species A Ahond, BF Bowden, JC Coll, J Fourneron and SJ Mitchell Structure 13C NMR ̼Æ×Ä£Äâͼ 82 . (-)-bicyclogermacrene ÏàËÆ¶È:53.3% Chemistry & Biodiversity 2008 Vol. 5 2449 Furanocembranoids from the Soft Corals Sinularia asterolobata and Litophyton arboreum Daniela Grote, Hans-Martin Dahse, and Karlheinz Seifert Structure 13C NMR ̼Æ×Ä£Äâͼ 83 . 15-Hydroxy-Tmuurolol C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 99-101 T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 84 . T-Muurolol C15H26O ÏàËÆ¶È:53.3% Journal of Natural Products 2009 72 99-101 T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 85 . eremophil-6-en-11-ol C15H26O ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2008 Vol. 91 1712 Two New Eremophilane-Type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana (Hemsl.) Greenm Cai-FangWang, Yu Zhao, Yan-Ze Liu, and Zhen-Zhong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 86 . (6¦Á,8¦Á)-6-hydroxyeremophil-7(11)-en-12,8-olide C15H22O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2006 Vol. 89 915 Terpenoids from the Roots of Ligularia muliensis Qiu-Hong Wu, Chun-Mei Liu, Yan-Jun Chen, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 87 . (3¦Â)-eudesm-4(14)-ene-3,11-diol ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2004 Vol. 87 1446 Eudesmane-Type Sesquiterpene Derivatives from Saussurea conica Cheng-Qi Fan, Zha-Jun Zhan, Hui Li, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 88 . Isom¨¦re cis(1S,3S,4S,6S) ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2001 Vol. 84 2430 Epoxyesters p-menthaniques et pinaniques en milieu basique -Parfum de noix de coco Marie-Jos¨¦phe Bourgeois et Evelyne Montaudon Structure 13C NMR ̼Æ×Ä£Äâͼ 89 . Isom¨¦re trans (1R,3R,4R,6S) ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2001 Vol. 84 2430 Epoxyesters p-menthaniques et pinaniques en milieu basique -Parfum de noix de coco Marie-Jos¨¦phe Bourgeois et Evelyne Montaudon Structure 13C NMR ̼Æ×Ä£Äâͼ 90 . elongatol A C15H24O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2007 55(5) 762-765 Nardosinane Sesquiterpenoids from the Formosan Soft Coral Nephthea elongata Shang-Kwei WANGa and Chang-Yih DUH Structure 13C NMR ̼Æ×Ä£Äâͼ 91 . 15-hydroxyallo-cedrol C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 2007 68 2409-2414 Sesquiterpenes from the wood of Juniperus lucayana Yarelis Ort¨ªz Nuñez, Iraida Spengler Salabarria, Isidro G. Collado,Rosario Hern¨¢ndez-Gal¨¢n Structure 13C NMR ̼Æ×Ä£Äâͼ 92 . (-)-epi-cedrol ÏàËÆ¶È:53.3% Phytochemistry 2003 64 303-323 Terpenoids from the seeds of Artemisia annua Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy Structure 13C NMR ̼Æ×Ä£Äâͼ 93 . (-)-amorpha-4,7(11)-diene ÏàËÆ¶È:53.3% Phytochemistry 2002 61 79-91 Volatile components from European liverworts Marsupella emarginata, M. aquatica and M. alpina Adewale Martins Adio, Claudia Paua, Wilfried A. König, Hermann Muhle Structure 13C NMR ̼Æ×Ä£Äâͼ 94 . (-)-lupanine ÏàËÆ¶È:53.3% Phytochemistry 2002 61 975-978 Quinolizidine alkaloids from the curare adjuvant Clathrotropis glaucophylla Anne-Lise Sagen, J¨¹rg Gertsch, Rita Becker, Jörg Heilmann, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 95 . illudiolone C15H24O3 ÏàËÆ¶È:53.3% Phytochemistry 2002 61 395-398 Sesquiterpenes from Omphalotus illudens Trevor C. McMorris, A. Kashinatham, Ricardo Lira, Henrik Rundgren, Peter K. Gantzel,Michael J. Kelner, Robin Dawe Structure 13C NMR ̼Æ×Ä£Äâͼ 96 . compound 5 C15H24 ÏàËÆ¶È:53.3% Phytochemistry 2001 58 969-972 ent-Daucane and acorane sesquiterpenes from¡ÁCupressocyparis leylandii foliage Laurence G. Cool Structure 13C NMR ̼Æ×Ä£Äâͼ 97 . halichonadin F C15H27N ÏàËÆ¶È:53.3% Journal of Natural Products 2008 71(7) 1301-1303 Halichonadin F and the Cu(I) Complex of Halichonadin C from the Sponge Halichondria sp. Haruaki Ishiyama, Shingo Kozawa, Kazuki Aoyama,Yuzuru Mikami, Jane Fromont, and Jun¡¯ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 98 . mairetolide F C15H22O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2006 69 1471-1475 Eremophilanes from Senecio mairetianus and Some Reaction Products Ana-L. Prez-Castorena, Amira Arciniegas, S. Laura Guzmn, Jos Luis Villaseor, and Alfonso Romo de Vivar Structure 13C NMR ̼Æ×Ä£Äâͼ 99 . (-)-(1R,7S,-10R)-1-hydroxy-11-norcadinan-5-en-4-one C14H22O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2005 68 1309-1313 Norsesquiterpenes from the Brown Alga Dictyopteris divaricata Fuhang Song, Xiuli Xu, Shuai Li, Sujuan Wang, Jielu Zhao, Peng Cao, Yongchun Yang, Xiao Fan, Jiangong Shi, Lan He, and Yang L Structure 13C NMR ̼Æ×Ä£Äâͼ 100 . (4S,9S,10R)-4,10,11-tribromo-10,11-seco-lippifoli-1(6)-en-5-one ÏàËÆ¶È:53.3% Journal of Natural Products 2005 68 659-665 Absolute Configuration of Lippifoliane and Africanane Derivatives Carlos M. Cerda-Garca-Rojas, Angelina del C. Coronel, Marina E.P. de Lampasona, Csar A. N. Cataln, and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 101 . 5¦Á,7¦Á,10¦ÂH-3-patchoulen-2-one C15H22O ÏàËÆ¶È:53.3% Journal of Natural Products 2004 67 914-917 Three New Sesquiterpenes from Croton arboreous A. Berenice Aguilar-Guadarrama, and Mara Yolanda Rios Structure 13C NMR ̼Æ×Ä£Äâͼ 102 . (4R,5S,6R,7R,11S)-12-Hydroxy-1(10)-aromadendren-14-al C15H22O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2004 67 799-805 Isolation of a Library of Aromadendranes from Landolphia dulcis and Its Characterization Using the VolSurf Approach Brian Skole, Flemming S. Jrgensen, Bogdan A. Budnik, Patrick Ekpe, and Jerzy W. Jaroszewski Structure 13C NMR ̼Æ×Ä£Äâͼ 103 . 10¦Á,15-dihydroxyamorph-4-en-3-one C15H24O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2007 70 304-306 Amorphane Sesquiterpenes from a Marine Streptomyces sp Shao Jie Wu,Serge Fotso, Fuchao Li, Song Qin, and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 104 . 5¦Â,8¦Â-epidioxy-11-hydroxy-6-eudesmene C15H24O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2007 70 1449-1453 Sesquiterpenoids and Artificial 19-Oxygenated Steroids from the Formosan Soft Coral Nephthea erecta Shi-Yie Cheng,Chang-Feng Dai, and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 105 . 8¦Â-hydroxyprespatane C15H24O ÏàËÆ¶È:53.3% Journal of Natural Products 2007 70 1449-1453 Sesquiterpenoids and Artificial 19-Oxygenated Steroids from the Formosan Soft Coral Nephthea erecta Shi-Yie Cheng,Chang-Feng Dai, and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 106 . 8¦Â-hydroperoxyprespatane C15H24O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2007 70 1449-1453 Sesquiterpenoids and Artificial 19-Oxygenated Steroids from the Formosan Soft Coral Nephthea erecta Shi-Yie Cheng,Chang-Feng Dai, and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 107 . compound 2 ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 1319-1322 African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd Structure 13C NMR ̼Æ×Ä£Äâͼ 108 . compound 3 ÏàËÆ¶È:53.3% Journal of Natural Products 2002 65 1319-1322 African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd Structure 13C NMR ̼Æ×Ä£Äâͼ 109 . (4S,5S,6¦Á,7¦Á,10R)-eudesma-5-en-11-ol epoxide C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 393-395 Oxygenated Sesquiterpenoids from a Nonpoisonous Sardinian Chemotype of Giant Fennel (Ferula communis) Giovanni Appendino, Giancarlo Cravotto, Olov Sterner, and Mauro Ballero Structure 13C NMR ̼Æ×Ä£Äâͼ 110 . manshurolide ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 415-418 Sesquiterpene Esters of Aristolochic Acid from the Root and Stem of Aristolochia heterophylla Tian-Shung Wu, Yu-Yi Chan, Yann-Lii Leu, and Zong-Tsi Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 111 . 2,6,10-trimethyl-2-undecen-6-ol C14H28O ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 214-218 Nuapapuin A and Sigmosceptrellins D and E: New Norterpene Cyclic Peroxides from a Southern Australian Marine Sponge, Sigmosceptrella sp. Simon P. B. Ovenden and Robert J. Capon Structure 13C NMR ̼Æ×Ä£Äâͼ 112 . 1,10-seco-4¦Î -hydroxy-muurol-5-ene-1,10-diketone C15H24O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 549-553 Muurolane Sesquiterpenes from Illicium tsangii Koon-Sin Ngo, Wing-Tak Wong, and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 113 . dihydroartemisinic acid ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 430-433 Isolation and Identification of Dihydroartemisinic Acid from Artemisia annua and Its Possible Role in the Biosynthesis of Artemisinin T. Eelco Wallaart, Wim van Uden, Heidi G. M. Lubberink, Herman J. Woerdenbag, Niesko Pras, and Wim J. Quax Structure 13C NMR ̼Æ×Ä£Äâͼ 114 . (8R)-8-hydroxypatchoulol C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 437-440 Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 115 . triterpenoid C30H50O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 653-654 A New Acyclic Diketotriterpenoid Isolated from the Indonesian Marine Sponge Hyrtios erectus David E. Williams, Akbar Tahir, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 116 . 3-ketodihydroartemisinic acid ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 790-793 Semisynthesis of 3-¦Â-Hydroxyartemisinin Nancy Acton Structure 13C NMR ̼Æ×Ä£Äâͼ 117 . compound 9 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 790-793 Semisynthesis of 3-¦Â-Hydroxyartemisinin Nancy Acton Structure 13C NMR ̼Æ×Ä£Äâͼ 118 . 7¦ÂH-eudesm-2-ene-4¦Á,11-diol C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 22-28 Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ 119 . carissone ÏàËÆ¶È:53.3% Journal of Natural Products 1996 59 409-411 Constituents of Persea japonica Chao-Chiun Wang, Chang-Sheng Kuoh and Tian-Shung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 120 . compound 2 C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1996 59 866-868 Drimane Sesquiterpenes from the Sponge Dysidea fusca A. Montagnac, M.-T. Martin, C. Debitus, and M. Païs Structure 13C NMR ̼Æ×Ä£Äâͼ |

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