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![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() 1 . clovandiol ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2013 44 2195-2199 Chemical constituents in stems of Zhuang Medicine Alsophila spinulosa LU Ru-mei, CAO Min, LIAO Peng-ying, WEI Jian-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 12 ÏàËÆ¶È:62.5% Angewandte Chemie International Edition 2012 51 7572-7576 A Synthesis of Echinopine B Theo D. Michels, Matthew S. Dowling, and Christopher D. Vanderwal Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 27 C17H24O2 ÏàËÆ¶È:62.5% Angewandte Chemie International Edition 2012 51 7572-7576 A Synthesis of Echinopine B Theo D. Michels, Matthew S. Dowling, and Christopher D. Vanderwal Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (-)-Clovane-2,9-diol ÏàËÆ¶È:60% Molecules 2008 13 2474-2481 Norcyperone, a Novel Skeleton Norsesquiterpene from Cyperus rotundus L. Yan Xu, Hong-Wu Zhang, Chang-Yuan Yu, Yang Lu, Ying Chang and Zhong-Mei Zou Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . clovandiol ÏàËÆ¶È:60% Journal of Natural Products 1984 Vol 47 1042-1045 Terpenoids From Viguiera excelsa and Viguiera oaxacana Guillermo Delgado, Hugo C¨¢rdenas, Guadalupe Pel¨¢ez, Alfonso Romo de Vivar, Rogelio Pereda-Miranda Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2,2,6,9-Tetramethyltricyclo [5.2.2.0(3.7) ]undecan-9-ol C15H26O ÏàËÆ¶È:60% Phytochemistry 1996 41 1361-1365 Terpenes from heartwood of Juniperus chinensis Jim-Min Fang, Ying-Chih Chen, Beng-Wern Wang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (3S,8R,9R)-isocaryolane-3,8,9-triol C15H26O3 ÏàËÆ¶È:60% 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 8 . clovane-2,9-diol ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2005 36 1619-1620 ÏÁ°êӥצ»¨µÄ±¶°ëÝÆÀà³É·ÖÑо¿ ³Â¹âÓ¢;Öì¹úÔª;º«³¤ÈÕ;ÀîÇìÑó;·½ºêÑ«;±ÏºÍƽ Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Clovane-2¦Â,9¦Á-diol C15H26O2 ÏàËÆ¶È:60% Pharmazie 2004 59 807-811 A new furobenzopyranone and other constituents from Anaphalis lactea Ai-Xia Wang, Qi Zhang, and Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (1S,4S,7S,9S)-5,5,7,9-tetramethyltricyclo[5.4.0.0(4,9)]-undecen-8-one C15H24O ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2001 37 1430-1434 Rearrangements of Neoclovene Epoxides in Acidic Media T. M. Khomenko, D. V. Korchagina, Yu. V. Gatilov and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N,N-hexane-1,6-diyl-bis(cytisinecarbamide) C30H70N6O4 ÏàËÆ¶È:60% Chemistry of Natural Compounds 2012 48 629-634 Synthesis and specific nootropic activity of (¨C)-cytisine derivatives with carbamide and thiocarbamide moieties in their structure I. P. Tsypysheva, A. V. Koval¡¯skaya, N. S. Makara, A. N. Lobov and I. A. Petrenko, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 23(major) C14H18 ÏàËÆ¶È:60% Angewandte Chemie International Edition 2012 51 7572-7576 A Synthesis of Echinopine B Theo D. Michels, Matthew S. Dowling, and Christopher D. Vanderwal Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 1¦ÂH,5¦ÁH,7¦ÂH-Guaia-3,10(14)-dien-11-ol C15H24O ÏàËÆ¶È:60% European Journal of Organic Chemistry 1996 1996 99-101 Two New Guaiadiene Derivatives Isolated from Thuja occidentalis L. Wood Oil Peter Weyerstahl, Helga Marschall and Guy Collin Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . dihydrolaurene C15H22 ÏàËÆ¶È:60% Australian Journal of Chemistry 1976 29 2533-2539 New laurene derivatives from Laurencia filiformis R Kazlauskas, PT Murphy, RJ Quinn and RJ Wells Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Toxicodenane C C15H24O2 ÏàËÆ¶È:60% Organic Letters 2013 15 3602-3605 Sesquiterpenoids with New Carbon Skeletons from the Resin of Toxicodendron vernicifluum as New Types of Extracellular Matrix Inhibitors Jiang-Bo He, Jie Luo, Li Zhang, Yong-Min Yan, and Yong-Xian Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 8-[methyl(4-phenylbutyl)amino]caffeine C19H25N5O2 ÏàËÆ¶È:58.8% Bioorganic & Medicinal Chemistry 2011 19 7507-7518 Thio- and aminocaffeine analogues as inhibitors of human monoamine oxidase Hermanus P. Booysen, Christina Moraal, Gisella Terre¡¯Blanche, An¨¦l Petzer, Jacobus J. Bergh, Jacobus P. Petzer Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . pogostol O-methyl ether C16H28O ÏàËÆ¶È:56.2% Journal of Natural Products 1997 60 1054-1056 Pogostol O-Methyl Ether and Artabotrol: Two Novel Sesquiterpenes from the Stem Bark of Artabotrys stenopetalus Theophilus C. Fleischer, Roger D. Waigh, and Peter G. Waterman Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 9-epi-9-isocyanopupukeanane C16H25N ÏàËÆ¶È:56.2% Tetrahedron Letters 1990 31 5623-5624 Co-occurrence of 9-isocyanopupukeanane and its C-9 epimer in the nudibranch phyllidia bourguini N. Fusetani, H.J. Wolstenholme, S. Matsunaga Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (1R,3S,5R,6S,7S,9R)-(-)-9-isothiocyanatopupukeanane C16H25NS ÏàËÆ¶È:56.2% Australian Journal of Chemistry 1997 50 1123-1127 Terpene Metabolites from the Tropical Marine Sponge Axinyssa sp. nov. Jamie S. Simpson,, Mary J. Garson,, John N. A. Hooper,, Edith I. Cline and Cindy K. Angerhofer Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Ziza-6(13)-en-12-yl methyl ether ÏàËÆ¶È:56.2% Flavour and Fragrance Journal 2000 15 61-83 1,7-Cyclogermacra-1(10),4-dien-15-al, a sesquiterpene with a novel skeleton, and other sesquiterpenes from Haitian vetiver oil Peter Weyerstahl, Helga Marschall, Ute Splittgerber and Dietmar Wolf Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . tetrahydromyricoidine ÏàËÆ¶È:55.5% Tetrahedron 1988 44 4521-4526 Myricoidine and dihydromyricoidine, two new macrocyclic spermidine alkaloids from clerodendrum myricoides Sanvura Bashwira, Claude Hootele Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . bazzanenoxide C15H22O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2006 54(9) 1347-1349 Bazzanane Sesquiterpenoids from the New Zealand Liverwort Frullania falciloba Fumihiro NAGASHIMA,Masao TOYOTA, and Yoshinori ASAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . cyclomyltaylane- 1¦Â,5¦Á-diol C15H24O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2006 54(7) 996-1003 Isolation and Structures of New Cyclomyltaylane and ent-Chamigrane-Type Sesquiterpenoids from the Liverwort Reboulia hemishaerica andTheir Biotransformation by the Fungus Aspergillus niger Mai FURUSAWA,Toshihiro HASHIMOTO,Yoshiaki NOMA,and Yoshinori ASAKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 4S-3¦Á-hydroxycadin-10(15)-ene ÏàËÆ¶È:53.3% Phytochemistry 2002 59 489-492 Biotransformation of cadina-4,10(15)-dien-3-one and 3a-hydroxycadina-4,10(15)-diene by Curvularia lunata ATCC 12017 Dwight O. Collins, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . keto-acid ÏàËÆ¶È:53.3% Phytochemistry 2001 58 799-810 Chemical study of the essential oil of Cyperus rotundus Mesmin Mekem Sonw, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 5 C15H26O ÏàËÆ¶È:53.3% Journal of Natural Products 2003 66 1097-1100 A Novel 5-HT Receptor Ligand and Related Cytotoxic Compounds from an Acid Mine Waste Extremophile Andrea A. Stierle, Donald B. Stierle, Eric Goldstein,Keith Parker,Tim Bugni, Chad Baarson,Julie Gress, and Danielle Blake Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 4,5-dihydro-¦Â-caryophyllene-14-al C15H24O ÏàËÆ¶È:53.3% Journal of Natural Products 2000 63 902-904 New Caryophyllene Derivatives from Betula litwinowii Bet¨¹l Demirci,K. H¨¹sn¨¹Can Bas¸er,Fatih Demirci, and Mark T. Hamann Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . (-)-clovane-2,9-diol C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1996 59 1084-1086 Sesquiterpenes from Baeckea frutescens Wing-Yan Tsui and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (4S)-3¦Á-hydroxycadin-10(15)-ene C15H26O ÏàËÆ¶È:53.3% Phytochemistry 2000 54 39-45 Biotransformation of cadinane sesquiterpenes by Beauveria bassiana ATCC 7159 Greg O. Buchanan, Lawrence A.D. Williams, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (4R)-3¦Á-hydroxycadin-10(15)-ene C15H26O ÏàËÆ¶È:53.3% Phytochemistry 2000 54 39-45 Biotransformation of cadinane sesquiterpenes by Beauveria bassiana ATCC 7159 Greg O. Buchanan, Lawrence A.D. Williams, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 10-epi-¦Ã-eudesmol C15H26O ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1985 33 1148-1153 Agarofuran-, Eudesmane-and Eremophilane-Type Sesquiterpenoids from Alpinia japonica (THUNB.) MIQ. HIDEJI ITOKAWA,HIROSHI MORITA,KINZO WATANABE,SUSUMU MIHASHI and YOICHI IITAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 7 C15H24O ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1987 35 124-135 Marine Natural Products. XVII. Nephtheoxydiol, a New Cytotoxic Hydroperoxy-Germacrane Sesquiterpene, and Related Sesquiterpenoids from an Okinawan Soft Coral of Nephthea sp. (Nephtheidae) ISAO KITAGAWA,ZHENG CUI,BYENG WHA SON,MOTOMASA KOBAYASHI and YOSHIMASA KYOGOKU Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 3¦Â-hydroxy-4,14-cyclogermacra-11-en-9-one C15H24O2 ÏàËÆ¶È:53.3% Chinese Chemical Letters 2005 16 915-917 A New Sesquiterpene from the Roots of Biondia hemsleyana Xing Gen TAN, Pei CAO, Shu Lin PENG, Li Sheng DING Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . (-)-clovane-2,9-diol ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 2009 34 2765-2767 Bioactive constituents from whole herbs of Vernonia cinerea (¢ò) ZHU Huaxu, TANG Yuping, MIN Zhida, GONG Zhunan Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . reneilmol C15H28O3 ÏàËÆ¶È:53.3% Phytochemistry 1999 52 1095-1099 Anti-plasmodial sesquiterpenoids from the African Reneilmia cincinnata Maguerite H.K. Tchuendem, James A. Mbah, Apollinaire Tsopmo, J. Foyere Ayafor, Olov Sterner, Christopher C. Okunjic, Maurice M. Iwu, Brian M. Schuster Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 7-epi-¦Ã-eudesmol C15H26O ÏàËÆ¶È:53.3% Phytochemistry 1998 47 1085-1088 Eudesmane sesquiterpenes from laggera alata Phila Raharivelomanana, Jean-Pierre Bianchini, Armand R. P. Ramanoelina, Jean R. E. Rasoarahona, Robert Faure, Aime Cambon Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . argutenol ÏàËÆ¶È:53.3% Natural Product Sciences 1999 5 85-87 Two New Sesquiterpenes from Pluchea arguta Ahmad, Viqar Uddin; Zahid, Muhammad; Khatoon, Rasheeda; Ali, Zulfiqar; Abbas, Muhammad; Iqbal, Muhammad Zafar Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 7-Epi-¦Ã-eudesmol C15H26O ÏàËÆ¶È:53.3% Phytochemistry 1995 39 603-607 Sesquiterpenes from leaves of Cryptomeria japonica Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . rel-(1S,4S,SR,7R,10R)-10-Desmethyl-1-methyl-11-eudesmene C15H26O ÏàËÆ¶È:53.3% Phytochemistry 1995 39 849-852 10-desmethyl-1-methyl-eudesmanes from Ocotea corymbosa Juceni Pereira Chavez, Otto R. Gottlieb, Massayoshi Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 9¦Â,10¦Á-Dihydroxytrichodiene ÏàËÆ¶È:53.3% Phytochemistry 1993 32 93-104 Potential inhibitors of trichothecene biosynthesis in Fusarium culmorum: Epoxidation of a trichodiene derivative Andrew R. Hesketh, Linden gledhill, Barrie W. Bycroft, Paul M. Dewick, John Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . (1S,6R,9R)-14-hydroxycaryophyll-2(15)-en-7-one C15H24O2 ÏàËÆ¶È:53.3% Phytochemistry 1992 31 2409-2413 Caryophyllene derivatives from Pulicaria dysenterica J.Alberto Marco, Juan F. Sanz, Remedios Albiach Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . compound 15 ÏàËÆ¶È:53.3% Phytochemistry 1991 30 3343-3347 Guaiane sesquiterpenes from agarwood Masakazu Ishihara, Tomoyuki Tsuneya, Kenji Uneyama Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . cycloisolongifol-3¦Â,5¦Â,11¦Á-triol C15H24O3 ÏàËÆ¶È:53.3% Zeitschrift f¨¹r Naturforschung B 2006 61b 1035-1038 Microbial Metabolism of (+)-Cycloisolongifol-5¦Â-ol Muhammad Iqbal Choudhary, Waseem Kausar, Zafar Ali Siddiqui, and Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . Pogostol C15H28O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2012 75 798-801 Guaiane Sesquiterpenes from Biscogniauxia nummularia Featuring Potent Antigerminative Activity Séverine Amand, Aude Langenfeld, Alain Blond, Joëlle Dupont, Bastien Nay, and Soizic Prado Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . compound 22 ÏàËÆ¶È:53.3% Phytochemistry 1990 29 757-763 Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . (1S,2S,4R,5S,8R,9R)-2,13-epoxy-9-clovanol C15H24O2 ÏàËÆ¶È:53.3% Phytochemistry 1990 29 757-763 Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . 2-cyclohexyl-6-methyl-4-oxo-5-oxa-1-ethoxycarbonyl-1-azaspiro[2,4]bicycloheptane C15H23NO4 ÏàËÆ¶È:53.3% Heterocycles 2005 65 1447-1454 Spiroaziridines from 4-Substituted ¦Á-Ylidene-¦Ã-butyro Lactones Tecla Gasperi, M. Antonietta Loreto,* Antonella Migliorini, and Paolo A. Tardella Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . Compound 13 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry Letters 1999 9 3465-3470 Antonios Kolocouris, Dimitrios Tataridis, George Fytas, Thomas Mavromoustakos, George B. Foscolos, Nicolas Kolocouris, Erik De Clercq Antonios Kolocouris, Dimitrios Tataridis, George Fytas, Thomas Mavromoustakos, George B. Foscolos, Nicolas Kolocouris, Erik De Clercq Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . compound 3 ÏàËÆ¶È:53.3% Phytochemistry 1986 25 1161-1165 Carotane sesquiterpenes from Ferula linkii Jesus G. Diaz, Braulio M. Fraga, Antonio G. Gonz¨¢lez, Melchor G. Hernandez, Aurea Perales Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 8-chloromethyl-2-hydroxy-11-methylene-tricyclo[5.3.1.0]undecane C13H19ClO ÏàËÆ¶È:53.3% Tetrahedron Letters 2005 46 6449-6451 Efficient synthesis of 8,11-dimethylene-bicyclo[5.3.1]undecan-2-one Haining Gu, Wei Ming Xu, Thomas H. Kinstle Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . isodihydrolaurene C15H22 ÏàËÆ¶È:53.3% Bulletin of the Chemical Society of Japan 1982 55 1561-1563 Six New Sesquiterpenoids from the Red Alga Laurencia nipponica Yamada Teruaki Suzuki, Hajime Kikuchi, Etsuro Kurosawa Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . (2S,4R)-N-Boc-O-TBDMS-4-deuterio-4-cyanoprolinol ÏàËÆ¶È:53.3% Chemistry-A European Journal 2004 10 4708-4717 Final Elucidation of the Absolute Configuration of the Signal Metabolite Hormaomycin Boris D. Zlatopolskiy, Karin Loscha, Petra Alvermann, Sergei I. Kozhushkov, Sergej V. Nikolaev, Axel Zeeck and Armin de Meijere Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . compound 16 C15H28O2 ÏàËÆ¶È:53.3% Heterocycles 2001 54 765-776 Intramolecular Photocycloaddition of 2-Cycloalkenyl-1,3-dioxin-4-one. Stereoselective Synthesis of cis-Eudesmane-4,11-diols Toshihide Hatsui,* Ka Li, Akira Mori,* and Hitoshi Takeshita Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . di-tert-butyl-N-5-hexenyliminodicarboxylate C32H58N2O8 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2010 18 4917-4927 Development of chemical probes: Toward the mode of action of a methylene-linked di(aryl acetate) E1 Mark E.B. Smith, Richard M. Gunn, Evelyn Rosivatz, Lok H. Mak, R¨¹diger Woscholski, Helen C. Hailes Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . clavaminol N C15H31NO2 ÏàËÆ¶È:53.3% Tetrahedron 2009 65 4384-4388 Clavaminols G¨CN, six new marine sphingoids from the Mediterranean ascidian Clavelina phlegraea Anna Aiello, Ernesto Fattorusso, Antonella Giordano, Marialuisa Menna, Carmen Navarrete, Eduardo Muñoz Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . (1R,3S,6R,7R,8R,11S)-11-iodo-6-isopropyl-1,3-dimethyl-2-oxatricyclo[5.3.1.0(3,8)]undecane ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2004 40 337-345 Functionalization of the Allyl Fragment in (+)-¦Ä-Cadinol F. A. Valeev, I. P. Tsypysheva, A. M. Kunakova, O. Yu. Krasnoslobodtseva and O. V. Shitikova, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . 1,4-dimethyl-3-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-cyclohepta[c]pyridine C16H24N2 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2011 3815-3824 Nickel-Catalyzed [2+2+2] Cycloaddition of Diynes and Cyanamides Ryan M. Stolley, Michael T. Maczka and Janis Louie Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . compound 25 C12H20O3 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2011 1557-1569 Gold-Catalysed Activation of Epoxides: Application in the Synthesis of Bicyclic Ketals Rengarajan Balamurugan, Raveendra Babu Kothapalli and Ganesh Kumar Thota Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . comound 14 C15H20O3 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2010 6944-6948 Anionic Cascade Reaction Followed by Silylative Dieckmann Cyclization: A Straightforward Route to Tricyclic Fused Ring Systems Starting from Alkynyl Esters Tethered to Bicyclo[n.2.0]alkanones Vincent Rietsch, Laurence Miesch, Daisuke Yamashita and Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . (RS)-N-cyclohexyl-2,2,5,5-tetramethyl-3-(trichloroacetyl)-1,3-oxazolidine-4-carboxamide C16H25Cl3N2O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2012 95 1857-1870 A Manifold Three-Step Synthetic Route to Polycyclic Annulated Hydantoins via Cyclic Imines Fabian Brockmeyer, Denis Kröger, Timo Stalling, Pasqual Ullrich and J¨¹rgen Martens Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . [R-{R*,S*)]-¦Â-[[(1,1-dimethyIetfaoxy)carbonyl]amino]-¦Á-[tris(methylthio)methyl]cyclohexanepropanol C18H35NO3S3 ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 1993 36 2431-2447 Activated ketone based inhibitors of human renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, Sandra A. Smith, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . [S-(R,R)]-[1-(cyclohexylmethyl)-2-(dimethoxyphosphinyl)-2-hydroxyethyl]carbamic acid,1,1-dimethylethyl ester C16H32NO6P ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 1995 38 4557-4569 alpha.-Hydroxy Phosphinyl-Based Inhibitors of Human Renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, W. Lynn Rogers, Sandra A. Smith, Jack M. DeForrest, Robert S. Oehl, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . compound 18 C12H22NO5P ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 1995 38 4557-4569 alpha.-Hydroxy Phosphinyl-Based Inhibitors of Human Renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, W. Lynn Rogers, Sandra A. Smith, Jack M. DeForrest, Robert S. Oehl, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . euphoranin E C15H24O2 ÏàËÆ¶È:53.3% Indian Journal of Chemistry Section B 1996 35B 1308-1310 Diterpenes and sesquiterpene from two Euphorbia species-Structure elucidation of Euphorhylonal A and Euphoranin E Hao Chen & Zhong Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . 14-dehydroxyl daucucarotol C15H28O2 ÏàËÆ¶È:53.3% Chinese Science Bulletin 2013 58 1115-1119 New terpenoids from the roots of Jatropha curcas YANG YuanFeng, LIU JieQing, LI XuYang, LIU EnQian, LI ZhongRong, QIU MingHua Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . araguspongine B ÏàËÆ¶È:53.3% Heterocycles 1998 47 195-203 Isomerization of Dimeric 2,9-Disubstituted1-Oxaquinolizidine Alkaloids and Structural Revision of Araguspongines B and E, Isolated from a Marine Sponge of Xestospongia Sp. Motomasa Kobayashi, Yasuhisa Miyamoto, Shunji Aoki, Nobutoshi Murakami, Isao Kitagawa, Yasuko In, and Toshimasa Ishida Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . compound 1a C28H49D2N2O2 ÏàËÆ¶È:53.3% Heterocycles 1998 47 195-203 Isomerization of Dimeric 2,9-Disubstituted1-Oxaquinolizidine Alkaloids and Structural Revision of Araguspongines B and E, Isolated from a Marine Sponge of Xestospongia Sp. Motomasa Kobayashi, Yasuhisa Miyamoto, Shunji Aoki, Nobutoshi Murakami, Isao Kitagawa, Yasuko In, and Toshimasa Ishida Structure 13C NMR ̼Æ×Ä£Äâͼ 68 . endo-3-tert-butyl-exo-3-methylbicyclo[3.2.1]octan-2-one C12H20O ÏàËÆ¶È:53.3% Canadian Journal of Chemistry 1988 66 454-460 13C magnetic resonance studies 133. An examination of the effect of conformation on ¦Â-enolization in some bicyclo[3.2.1]octan-2-ones Michael T. M. Clements, Ross E. Klinck, Sriyawathie Peiris, Arthur J. Ragauskas, J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . trans-dihydrocarissone ÏàËÆ¶È:53.3% 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 70 . (1'R,2S,5R,6R)-2-(1'-bromoethyl)-2,5-dimethyl-6-(penta-4''-enyl)-tetrahydropyran C14H25BrO ÏàËÆ¶È:53.3% Tetrahedron 1982 38 1699-1703 New tetrahydropyrans from a marine sponge Original Research Article Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . (1'R,2S,5R,6R)-2-(1'-bromoethyl)-2,5-dimethyl-6-pentyltetrahydropyran C14H27BrO ÏàËÆ¶È:53.3% Tetrahedron 1982 38 1699-1703 New tetrahydropyrans from a marine sponge Original Research Article Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 72 . frabenol C15H26O2 ÏàËÆ¶È:53.3% Natural Product Communications 2011 6 763-766 A Novel Sesquiterpene Alcohol from Fimetariella rabenhorstii, an Endophytic Fungus of Aquilaria sinensis Mei-Hua Tao, Jian Yan, Xiao-Yi Wei, Dong-Li Li, Wei-Min Zhang and Jian-Wen Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 73 . compound 37 ÏàËÆ¶È:53.3% Flavour and Fragrance Journal 2000 15 61-83 1,7-Cyclogermacra-1(10),4-dien-15-al, a sesquiterpene with a novel skeleton, and other sesquiterpenes from Haitian vetiver oil Peter Weyerstahl, Helga Marschall, Ute Splittgerber and Dietmar Wolf Structure 13C NMR ̼Æ×Ä£Äâͼ 74 . 7-(2-Cyclohexylethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione C15H22N4O2 ÏàËÆ¶È:53.3% Synthesis 2014 46 1380-1388 N7-Tosyltheophylline (TsTh)£ºA Highly Efficient Reagent for the One-Pot Synthesis of N7-Alkyltheophyllines from Alcohols Soltani Rad, Mohammad Navid; Behrouz, Somayeh; Najafi, Hosnieh Structure 13C NMR ̼Æ×Ä£Äâͼ 75 . 1,3-Dimethyl-7-(octan-2-yl)-3,7-dihydro-1H-purine-2,6-dione C15H24N4O2 ÏàËÆ¶È:53.3% Synthesis 2014 46 1380-1388 N7-Tosyltheophylline (TsTh)£ºA Highly Efficient Reagent for the One-Pot Synthesis of N7-Alkyltheophyllines from Alcohols Soltani Rad, Mohammad Navid; Behrouz, Somayeh; Najafi, Hosnieh Structure 13C NMR ̼Æ×Ä£Äâͼ 76 . methyl (2'R,3'R,4'R,5'R)-2-[2'-pentyl-4',5'-isopropilidenedeoxytetrahydrofuran-3'-yl] acetate C15H26O5 ÏàËÆ¶È:53.3% Journal of the Brazilian Chemical Society 2007 18 284-290 Synthesis and Antifungal Activity of New Bis-g-lactones Analogous to Avenaciolide Andr¨¦ia da Silva Magaton, Mayura M. 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Sanz, Remedios Albiach Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . compound 15 ÏàËÆ¶È:53.3% Phytochemistry 1991 30 3343-3347 Guaiane sesquiterpenes from agarwood Masakazu Ishihara, Tomoyuki Tsuneya, Kenji Uneyama Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . cycloisolongifol-3¦Â,5¦Â,11¦Á-triol C15H24O3 ÏàËÆ¶È:53.3% Zeitschrift f¨¹r Naturforschung B 2006 61b 1035-1038 Microbial Metabolism of (+)-Cycloisolongifol-5¦Â-ol Muhammad Iqbal Choudhary, Waseem Kausar, Zafar Ali Siddiqui, and Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . Pogostol C15H28O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2012 75 798-801 Guaiane Sesquiterpenes from Biscogniauxia nummularia Featuring Potent Antigerminative Activity Séverine Amand, Aude Langenfeld, Alain Blond, Joëlle Dupont, Bastien Nay, and Soizic Prado Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . compound 22 ÏàËÆ¶È:53.3% Phytochemistry 1990 29 757-763 Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . (1S,2S,4R,5S,8R,9R)-2,13-epoxy-9-clovanol C15H24O2 ÏàËÆ¶È:53.3% Phytochemistry 1990 29 757-763 Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . 2-cyclohexyl-6-methyl-4-oxo-5-oxa-1-ethoxycarbonyl-1-azaspiro[2,4]bicycloheptane C15H23NO4 ÏàËÆ¶È:53.3% Heterocycles 2005 65 1447-1454 Spiroaziridines from 4-Substituted ¦Á-Ylidene-¦Ã-butyro Lactones Tecla Gasperi, M. Antonietta Loreto,* Antonella Migliorini, and Paolo A. Tardella Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . Compound 13 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry Letters 1999 9 3465-3470 Antonios Kolocouris, Dimitrios Tataridis, George Fytas, Thomas Mavromoustakos, George B. Foscolos, Nicolas Kolocouris, Erik De Clercq Antonios Kolocouris, Dimitrios Tataridis, George Fytas, Thomas Mavromoustakos, George B. Foscolos, Nicolas Kolocouris, Erik De Clercq Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . compound 3 ÏàËÆ¶È:53.3% Phytochemistry 1986 25 1161-1165 Carotane sesquiterpenes from Ferula linkii Jesus G. Diaz, Braulio M. Fraga, Antonio G. Gonz¨¢lez, Melchor G. Hernandez, Aurea Perales Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 8-chloromethyl-2-hydroxy-11-methylene-tricyclo[5.3.1.0]undecane C13H19ClO ÏàËÆ¶È:53.3% Tetrahedron Letters 2005 46 6449-6451 Efficient synthesis of 8,11-dimethylene-bicyclo[5.3.1]undecan-2-one Haining Gu, Wei Ming Xu, Thomas H. Kinstle Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . isodihydrolaurene C15H22 ÏàËÆ¶È:53.3% Bulletin of the Chemical Society of Japan 1982 55 1561-1563 Six New Sesquiterpenoids from the Red Alga Laurencia nipponica Yamada Teruaki Suzuki, Hajime Kikuchi, Etsuro Kurosawa Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . (2S,4R)-N-Boc-O-TBDMS-4-deuterio-4-cyanoprolinol ÏàËÆ¶È:53.3% Chemistry-A European Journal 2004 10 4708-4717 Final Elucidation of the Absolute Configuration of the Signal Metabolite Hormaomycin Boris D. Zlatopolskiy, Karin Loscha, Petra Alvermann, Sergei I. Kozhushkov, Sergej V. Nikolaev, Axel Zeeck and Armin de Meijere Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . compound 16 C15H28O2 ÏàËÆ¶È:53.3% Heterocycles 2001 54 765-776 Intramolecular Photocycloaddition of 2-Cycloalkenyl-1,3-dioxin-4-one. Stereoselective Synthesis of cis-Eudesmane-4,11-diols Toshihide Hatsui,* Ka Li, Akira Mori,* and Hitoshi Takeshita Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . di-tert-butyl-N-5-hexenyliminodicarboxylate C32H58N2O8 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2010 18 4917-4927 Development of chemical probes: Toward the mode of action of a methylene-linked di(aryl acetate) E1 Mark E.B. Smith, Richard M. Gunn, Evelyn Rosivatz, Lok H. Mak, R¨¹diger Woscholski, Helen C. Hailes Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . clavaminol N C15H31NO2 ÏàËÆ¶È:53.3% Tetrahedron 2009 65 4384-4388 Clavaminols G¨CN, six new marine sphingoids from the Mediterranean ascidian Clavelina phlegraea Anna Aiello, Ernesto Fattorusso, Antonella Giordano, Marialuisa Menna, Carmen Navarrete, Eduardo Muñoz Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . (1R,3S,6R,7R,8R,11S)-11-iodo-6-isopropyl-1,3-dimethyl-2-oxatricyclo[5.3.1.0(3,8)]undecane ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2004 40 337-345 Functionalization of the Allyl Fragment in (+)-¦Ä-Cadinol F. A. Valeev, I. P. Tsypysheva, A. M. Kunakova, O. Yu. Krasnoslobodtseva and O. V. Shitikova, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . 1,4-dimethyl-3-(pyrrolidin-1-yl)-6,7,8,9-tetrahydro-5H-cyclohepta[c]pyridine C16H24N2 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2011 3815-3824 Nickel-Catalyzed [2+2+2] Cycloaddition of Diynes and Cyanamides Ryan M. Stolley, Michael T. Maczka and Janis Louie Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . compound 25 C12H20O3 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2011 1557-1569 Gold-Catalysed Activation of Epoxides: Application in the Synthesis of Bicyclic Ketals Rengarajan Balamurugan, Raveendra Babu Kothapalli and Ganesh Kumar Thota Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . comound 14 C15H20O3 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2010 6944-6948 Anionic Cascade Reaction Followed by Silylative Dieckmann Cyclization: A Straightforward Route to Tricyclic Fused Ring Systems Starting from Alkynyl Esters Tethered to Bicyclo[n.2.0]alkanones Vincent Rietsch, Laurence Miesch, Daisuke Yamashita and Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . (RS)-N-cyclohexyl-2,2,5,5-tetramethyl-3-(trichloroacetyl)-1,3-oxazolidine-4-carboxamide C16H25Cl3N2O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2012 95 1857-1870 A Manifold Three-Step Synthetic Route to Polycyclic Annulated Hydantoins via Cyclic Imines Fabian Brockmeyer, Denis Kröger, Timo Stalling, Pasqual Ullrich and J¨¹rgen Martens Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . [R-{R*,S*)]-¦Â-[[(1,1-dimethyIetfaoxy)carbonyl]amino]-¦Á-[tris(methylthio)methyl]cyclohexanepropanol C18H35NO3S3 ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 1993 36 2431-2447 Activated ketone based inhibitors of human renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, Sandra A. Smith, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . [S-(R,R)]-[1-(cyclohexylmethyl)-2-(dimethoxyphosphinyl)-2-hydroxyethyl]carbamic acid,1,1-dimethylethyl ester C16H32NO6P ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 1995 38 4557-4569 alpha.-Hydroxy Phosphinyl-Based Inhibitors of Human Renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, W. Lynn Rogers, Sandra A. Smith, Jack M. DeForrest, Robert S. Oehl, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . compound 18 C12H22NO5P ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 1995 38 4557-4569 alpha.-Hydroxy Phosphinyl-Based Inhibitors of Human Renin Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, W. Lynn Rogers, Sandra A. Smith, Jack M. DeForrest, Robert S. Oehl, Edward W. Petrillo Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . euphoranin E C15H24O2 ÏàËÆ¶È:53.3% Indian Journal of Chemistry Section B 1996 35B 1308-1310 Diterpenes and sesquiterpene from two Euphorbia species-Structure elucidation of Euphorhylonal A and Euphoranin E Hao Chen & Zhong Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . 14-dehydroxyl daucucarotol C15H28O2 ÏàËÆ¶È:53.3% Chinese Science Bulletin 2013 58 1115-1119 New terpenoids from the roots of Jatropha curcas YANG YuanFeng, LIU JieQing, LI XuYang, LIU EnQian, LI ZhongRong, QIU MingHua Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . araguspongine B ÏàËÆ¶È:53.3% Heterocycles 1998 47 195-203 Isomerization of Dimeric 2,9-Disubstituted1-Oxaquinolizidine Alkaloids and Structural Revision of Araguspongines B and E, Isolated from a Marine Sponge of Xestospongia Sp. Motomasa Kobayashi, Yasuhisa Miyamoto, Shunji Aoki, Nobutoshi Murakami, Isao Kitagawa, Yasuko In, and Toshimasa Ishida Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . compound 1a C28H49D2N2O2 ÏàËÆ¶È:53.3% Heterocycles 1998 47 195-203 Isomerization of Dimeric 2,9-Disubstituted1-Oxaquinolizidine Alkaloids and Structural Revision of Araguspongines B and E, Isolated from a Marine Sponge of Xestospongia Sp. Motomasa Kobayashi, Yasuhisa Miyamoto, Shunji Aoki, Nobutoshi Murakami, Isao Kitagawa, Yasuko In, and Toshimasa Ishida Structure 13C NMR ̼Æ×Ä£Äâͼ 68 . endo-3-tert-butyl-exo-3-methylbicyclo[3.2.1]octan-2-one C12H20O ÏàËÆ¶È:53.3% Canadian Journal of Chemistry 1988 66 454-460 13C magnetic resonance studies 133. An examination of the effect of conformation on ¦Â-enolization in some bicyclo[3.2.1]octan-2-ones Michael T. M. Clements, Ross E. Klinck, Sriyawathie Peiris, Arthur J. Ragauskas, J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . trans-dihydrocarissone ÏàËÆ¶È:53.3% 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 70 . (1'R,2S,5R,6R)-2-(1'-bromoethyl)-2,5-dimethyl-6-(penta-4''-enyl)-tetrahydropyran C14H25BrO ÏàËÆ¶È:53.3% Tetrahedron 1982 38 1699-1703 New tetrahydropyrans from a marine sponge Original Research Article Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . (1'R,2S,5R,6R)-2-(1'-bromoethyl)-2,5-dimethyl-6-pentyltetrahydropyran C14H27BrO ÏàËÆ¶È:53.3% Tetrahedron 1982 38 1699-1703 New tetrahydropyrans from a marine sponge Original Research Article Robert J. Capon, Emilio L. Ghisalberti, Phillip R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 72 . frabenol C15H26O2 ÏàËÆ¶È:53.3% Natural Product Communications 2011 6 763-766 A Novel Sesquiterpene Alcohol from Fimetariella rabenhorstii, an Endophytic Fungus of Aquilaria sinensis Mei-Hua Tao, Jian Yan, Xiao-Yi Wei, Dong-Li Li, Wei-Min Zhang and Jian-Wen Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 73 . compound 37 ÏàËÆ¶È:53.3% Flavour and Fragrance Journal 2000 15 61-83 1,7-Cyclogermacra-1(10),4-dien-15-al, a sesquiterpene with a novel skeleton, and other sesquiterpenes from Haitian vetiver oil Peter Weyerstahl, Helga Marschall, Ute Splittgerber and Dietmar Wolf Structure 13C NMR ̼Æ×Ä£Äâͼ 74 . 7-(2-Cyclohexylethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione C15H22N4O2 ÏàËÆ¶È:53.3% Synthesis 2014 46 1380-1388 N7-Tosyltheophylline (TsTh)£ºA Highly Efficient Reagent for the One-Pot Synthesis of N7-Alkyltheophyllines from Alcohols Soltani Rad, Mohammad Navid; Behrouz, Somayeh; Najafi, Hosnieh Structure 13C NMR ̼Æ×Ä£Äâͼ 75 . 1,3-Dimethyl-7-(octan-2-yl)-3,7-dihydro-1H-purine-2,6-dione C15H24N4O2 ÏàËÆ¶È:53.3% Synthesis 2014 46 1380-1388 N7-Tosyltheophylline (TsTh)£ºA Highly Efficient Reagent for the One-Pot Synthesis of N7-Alkyltheophyllines from Alcohols Soltani Rad, Mohammad Navid; Behrouz, Somayeh; Najafi, Hosnieh Structure 13C NMR ̼Æ×Ä£Äâͼ 76 . methyl (2'R,3'R,4'R,5'R)-2-[2'-pentyl-4',5'-isopropilidenedeoxytetrahydrofuran-3'-yl] acetate C15H26O5 ÏàËÆ¶È:53.3% Journal of the Brazilian Chemical Society 2007 18 284-290 Synthesis and Antifungal Activity of New Bis-g-lactones Analogous to Avenaciolide Andr¨¦ia da Silva Magaton, Mayura M. M. Rubinger, Fernando C. de Macedo J¨²nior and La¨¦rcio Zambolim Structure 13C NMR ̼Æ×Ä£Äâͼ 77 . (E)-tert-Butyl 6-(6-hydroxyhex-4-enamido)hexylcarba mate |

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