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²éѯ½á¹û£º¹²²éµ½322¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cinnamolide ÏàËÆ¶È:93.3% Journal of Natural Products 1992 Vol 55 1454 Drimane Sesquiterpene Lactones from Peniophora polygonia William A. Ayer, Latchezar S. Trifonov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . dendocarbin-A C15H24O2 ÏàËÆ¶È:73.3% Tetrahedron 2005 61 11032-11037 Pelseneeriol-1 and -2: new furanosesquiterpene alcohols from porostome nudibranch Doriopsilla pelseneeri Helena Gaspar, Margherita Gavagnin, Gonçalo Calado, Francesco Castelluccio, Ernesto Mollo, Guido Cimino Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 15 ÏàËÆ¶È:68.7% Phytochemistry 1994 35 713-719 Compounds with the labdane skeleton from Halimium viscosum Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . isodrimeninol ÏàËÆ¶È:66.6% Journal of Natural Products 2001 64 726-731 Dendocarbins A-N, New Drimane Sesquiterpenes from the Nudibranch Dendrodoris carbunculosa Yukako Sakio, Yoshiaki J. Hirano, Masahiko Hayashi, Kanki Komiyama,and Masami Ishibashi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . cis-dihydrocinnamolide ÏàËÆ¶È:66.6% Phytochemistry 1996 42 1361-1366 Sesquiterpenoids from the liverworts Bazzania trilobata and Porella canariensis Fumihiro Nagashima, Shiori Momosaki, Yûko Watanabe, Shigeru Takaoka, Siegfried Huneck, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . isodrimeniol ÏàËÆ¶È:66.6% Phytochemistry 1996 42 1361-1366 Sesquiterpenoids from the liverworts Bazzania trilobata and Porella canariensis Fumihiro Nagashima, Shiori Momosaki, Yûko Watanabe, Shigeru Takaoka, Siegfried Huneck, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . euryfuran ÏàËÆ¶È:66.6% Journal of Natural Products 1992 Vol 55 506 Isolation of Latrunculin A, 6,7-Epoxylatrunculin A, Fijianolide A, and Euryfuran from a New Genus of the Family Thorectidae Nanda K. Gulavita, Sarath P. Gunasekera, Shirley A. Pomponi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . drimendiol C15H26O2 ÏàËÆ¶È:66.6% Phytochemistry 1994 35 975-977 Drimendiol, a sesquiterpene from Drymis winterii Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Compound 1 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2005 43 82-84 A complete 1H and 13C NMR data assignment for four drimane sesquiterpenoids isolated from Drimys winterii Benjam¨ªn Rodr¨ªguez, Nelson Zapata, Pilar Medina and Elisa Viñuela Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . isodrimeninol ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2005 43 82-84 A complete 1H and 13C NMR data assignment for four drimane sesquiterpenoids isolated from Drimys winterii Benjam¨ªn Rodr¨ªguez, Nelson Zapata, Pilar Medina and Elisa Viñuela Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Iresin ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2005 43 339-342 1H and 13C assignments of three new drimenes from Iresine diffusa Humb. & Bonpl. ex Willd. Mar¨ªa Yolanda Rios and Laura ¨¢lvarez Berber Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . drimendiol ÏàËÆ¶È:66.6% Molecules 2013 18 2029-2051 Structural Requirements for the Antifungal Activities of Natural Drimane Sesquiterpenes and Analogues, Supported by Conformational and Electronic Studies Marcos Derita, Iv¨¢n Montenegro, Francisco Garibotto, Ricardo D. Enriz, Mauricio Cuellar Fritis and Susana A. Zacchino Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (-)-(5aS,9aS,9bR)-6,6,9a-Trimethyl-1,3,5,5a,6,7,8,9,9a,9b-decahydronaphtho[1,2-c]furan ÏàËÆ¶È:66.6% Molecules 2013 18 2029-2051 Structural Requirements for the Antifungal Activities of Natural Drimane Sesquiterpenes and Analogues, Supported by Conformational and Electronic Studies Marcos Derita, Iv¨¢n Montenegro, Francisco Garibotto, Ricardo D. Enriz, Mauricio Cuellar Fritis and Susana A. Zacchino Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . isodrimeninol ÏàËÆ¶È:66.6% Molecules 2013 18 2029-2051 Structural Requirements for the Antifungal Activities of Natural Drimane Sesquiterpenes and Analogues, Supported by Conformational and Electronic Studies Marcos Derita, Iv¨¢n Montenegro, Francisco Garibotto, Ricardo D. Enriz, Mauricio Cuellar Fritis and Susana A. Zacchino Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 5 C17H24O4 ÏàËÆ¶È:64.7% Journal of Natural Products 1997 60 1115-1120 Sesquiterpenoids of the Drimane Class from a Sponge of the Genus Dysidea Valerie J. Paul, Youngwan Seo, Ki Woong Cho, Jung-Rae Rho, Jongheon Shin, and Patricia R. Bergquist Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 11-ethoxycinnamolide C15H21O2 ÏàËÆ¶È:64.7% Phytochemistry 1985 24 1521-1524 Drimane-type sesqui- and norsesquiterpenoids from polygonum hydropiper Yoshiyasu Fukuyama, Tsuneo Sato, Iwao Miura, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . minor trans isomer 3,4,4a,5,6,7,8,8a-Octahydro-5,5,8a-trimethyl-1-trimethylsiloxynaphthalene ÏàËÆ¶È:64.2% Journal of Natural Products 2004 67 1996-2001 Correction of the Structure of a New Sesquiterpene from Cistus creticus ssp. creticus Konstantinos Hatzellis, Georgia Pagona, Apostolos Spyros,Costas Demetzos,and Haralambos E. Katerinopoulos Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . benzyl 2-propylpiperidine-1-carboxylate C16H23NO2 ÏàËÆ¶È:64.2% Heterocycles 2006 70 335-344 Enantioselective Synthesis of ent-Sedridine and (+)-Coniine via Proline-Catalyzed Mannich Reaction Kazuhiro Nagata, Kosuke Nishimura, Masashi Yokoya, and Takashi Itoh* Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . trans-dihydroconfertifolin ÏàËÆ¶È:64.2% Australian Journal of Chemistry 1997 50 341-347 Avarol and Related Compounds from the New Zealand Marine Sponge Dysidea sp. Michael Stewart, Patrick M. Fell, John W. Blunt and Murray H. G. Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (¡À)-1-benzyl-3-isobutyl-1,4-diazepine-2,5-dione C16H22O2N2 ÏàËÆ¶È:64.2% Tetrahedron 2012 68 9842-9852 Solution-phase synthesis of novel seven-membered cyclic dipeptides containing ¦Á- and ¦Â-amino acids Erika Jim¨¦nez-Gonz¨¢lez, C. Gabriela ¨¢vila-Ortiz, Rodrigo Gonz¨¢lez-Olvera, Jorge Vargas-Caporali, Georges Dewynter, Eusebio Juaristi Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 13,14,15,16-tetranor-7-Labden-17,12-olide ÏàËÆ¶È:62.5% Phytochemistry 1994 35 713-719 Compounds with the labdane skeleton from Halimium viscosum Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . methyl isodrimeninol C16H26O2 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry Letters 2002 12 477-482 Protective effects of polygodial and related compounds on ethanol-induced gastric mucosal lesions in rats: structural requirements and mode of action Hisashi Matsuda, Yutana Pongpiriyadacha, Toshio Morikawa, Yousuke Kashima, Kyoko Nakano, Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 13,14,15,16-tetranor-labd-7-en-l7,12-olide ÏàËÆ¶È:62.5% Natural Product Communications 2012 7 1139-1142 Bioactive-guided Identification of Labdane Diterpenoids from Aerial Parts of Aristeguietia glutinosa as anti-Trypanosoma cruzi agents Javier Varela, Mar¨ªa L. Lavaggi, Mauricio Cabrera, Alejandra Rodr¨ªguez, Patricio Miño, Ximena Chiriboga, Hugo Cerecetto and Mercedes Gonz¨¢lez Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . drimenal C15H24O ÏàËÆ¶È:60% Phytochemistry 2004 65 2583-2588 Bioactivity guided isolation of antifungal compounds from the liverwort Bazzania trilobata (L.) S.F. Gray Jochen M. Scher, John-Bryan Speakman, Josef Zapp, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . bacciferin B C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(4) 628-632 Terpenoids from the Stems of Cipadessa baccifera Li-Gen Lin, Chun-Ping Tang, Chang-Qiang Ke, Yi Zhang, and Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 7 C17H32O6S2 ÏàËÆ¶È:60% Journal of Natural Products 2001 64 348-349 Synthesis of (+)-Cyclozonarone and the Absolute Configuration of Naturally Occurring (-)-Cyclozonarone Manuel Cort¨¦s, Jaime A. Valderrama, Mauricio Cuellar, Ver¨®nica Armstrong, and Marcelo Preite Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . hurghamide-C C22H41NO3 ÏàËÆ¶È:60% Natural Product Research 1997 9 281-288 Hurghamides A-D, New N-Acyl-2-Methylene-¦Â-Alanine Methyl Esters from Red sea Hippospongia SP Yuewei Guo; Margherita Gavagnin; Ernesto Mollo; Guido Cimino; Nehal Aly Hamdy; Issa Fakhr; Maurizio Pansini Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . tricyclo[6.3.1.0(2.5)]dodec-6-en-8¦Á-ol C15H24O ÏàËÆ¶È:60% Journal of Natural Products 1990 Vol 53 1353 Chemistry of Sponges, X. New Sesquiterpenes from a Marine Sponge of the Genus Eurypon M. R. Kernan, R. C. Cambie, Patricia R. Bergquist Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3¦Â-hydroxycinnamolide ÏàËÆ¶È:60% Journal of Natural Products 1992 Vol 55 1454 Drimane Sesquiterpene Lactones from Peniophora polygonia William A. Ayer, Latchezar S. Trifonov Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . isodrimeninol ÏàËÆ¶È:60% Phytochemistry 1994 35 975-977 Drimendiol, a sesquiterpene from Drymis winterii Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 3-hydroxy-5-(2,6,6-trimethylcyclohex-1-enyl)-penta-2,4-dienethioic acid ethylamide C16H25NOS ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2007 44 167-176 Synthesis and reactions of the thioamide derivatives of methyl vinyl ketone Łukasz Groś,Aneta Wesołowska,Sławomir Westerlich and Tadeusz Jagodzi¨½ski Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 1¦Â,9¦Â-diacetoxymaalioxide C19H30O5 ÏàËÆ¶È:60% Heterocycles 2004 62 655-666 Biotransformation of (-)-Maalioxide by Aspergillus niger and Aspergillus cellulosae Toshihiro Hashimoto, Yoshiaki Noma, Yoshiaki Gotoh, Masami Tanaka, Shigeru Takaoka, and Yoshinori Asakawa* Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . dicarboxyl derivative C15H23O4 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry Letters 2002 12 477-482 Protective effects of polygodial and related compounds on ethanol-induced gastric mucosal lesions in rats: structural requirements and mode of action Hisashi Matsuda, Yutana Pongpiriyadacha, Toshio Morikawa, Yousuke Kashima, Kyoko Nakano, Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 11-bromo-8-drimene ÏàËÆ¶È:60% Tetrahedron 1998 54 5635-5650 Synthesis of wiedendiol-A and wiedendiol-B from labdane diterpenes Alejandro F. Barrero, Enrique J. Alvarez-Manzaneda, Rachid Chahboun Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . allohimachalol C15H26O ÏàËÆ¶È:60% 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 36 . isodrimendiol ÏàËÆ¶È:60% Molecules 2013 18 2029-2051 Structural Requirements for the Antifungal Activities of Natural Drimane Sesquiterpenes and Analogues, Supported by Conformational and Electronic Studies Marcos Derita, Iv¨¢n Montenegro, Francisco Garibotto, Ricardo D. Enriz, Mauricio Cuellar Fritis and Susana A. Zacchino Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (-)-(1S,8aS)-2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carbaldehyde ÏàËÆ¶È:60% Molecules 2013 18 2029-2051 Structural Requirements for the Antifungal Activities of Natural Drimane Sesquiterpenes and Analogues, Supported by Conformational and Electronic Studies Marcos Derita, Iv¨¢n Montenegro, Francisco Garibotto, Ricardo D. Enriz, Mauricio Cuellar Fritis and Susana A. Zacchino Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 7-epi-Helifolan-12-ol ÏàËÆ¶È:60% Flavour and Fragrance Journal 2001 16 50-60 Constituents of the acidic part of commercial Brazilian lantana oil Peter Weyerstahl, Helga Marschall and Christian Christiansen Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . polygodial 12¦Á-acetal ÏàËÆ¶È:58.8% Phytochemistry 1995 38 909-915 Phytotoxic sesquiterpenoids from Canella winterana Bai-Ping Ying, Galen Peiser, Yi-Yuan Ji, Kristina Mathias, Diana Tutko, Yih-Shen Hwang Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . andrachcinidine C13H25NO2 ÏàËÆ¶È:57.1% Journal of Natural Products 2000 63 762-764 Alkaloids of Andrachne aspera Sibel Mill and Claude Hootele Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . compound 9 C14H22O2 ÏàËÆ¶È:57.1% Journal of Natural Products 1997 60 1115-1120 Sesquiterpenoids of the Drimane Class from a Sponge of the Genus Dysidea Valerie J. Paul, Youngwan Seo, Ki Woong Cho, Jung-Rae Rho, Jongheon Shin, and Patricia R. Bergquist Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . hydrocarbon ÏàËÆ¶È:57.1% 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 43 . 1,3,4,7,7-pentamethyl-2-oxa-bicyclp[4.4.0]-dec-3-en (Isomer B) C14H24O ÏàËÆ¶È:57.1% Helvetica Chimica Acta 1976 59 727-737 Photochemische Reaktionen Zur Photochemie des Iso-methyl-¦Â,(E)-jonon-epoxid Beat Rudolf von Wartburg, Hans Richard Wolf und Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . compound 22 ÏàËÆ¶È:57.1% 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 45 . compound 2f C15H21NO ÏàËÆ¶È:57.1% Heterocycles 2010 81 2471-2478 Novel Application of Electrooxidative Method for the Cyclization of N-Benzyl-2-(hydroxymethyl)- and N-Benzyl-2-(2-hydroxyethyl)piperidines Mitsuhiro Okimoto, Takashi Yoshida, Masayuki Hoshi, and Kousuke Ohashi Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . (5S,8S,8aR)-(+)-8-methyl-5-pentyloctahydroindolizine C14H27N ÏàËÆ¶È:57.1% Heterocycles 2009 78 2589-2594 A Short Synthesis of Indolizidine (+)-209B from (3R,6S,8AS)-(-)-6-Methyl-3-phenyl-hexahydrooxazolo[3,2-a]pyridin-5-one Dino Gnecco, Ana M. Lumbreras, Joel L. Ter¨¢n, Alberto Galindo, Jorge R. Ju¨¢rez, Mar¨ªa L. Orea, Alejandro Castro, Ra¨²l G. Enr¨ªquez, and William F. Reynolds Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (6aS,9aR,9br)-6a-(2-methoxyethyl)octahydropyrrolo[3,2,1-ij]quinoline-2,9-dione C14H21NO3 ÏàËÆ¶È:57.1% Heterocycles 2004 62 787-792 A Formal Total Synthesis of (-)-Limaspermine Yu-ichi Fukuda, Mitsuru Shindo, and Kozo Shishido* Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . (2R,4aS,8aS)-Octahydro-5,5,8a-trimethyl-1H-spiro[naphthalene-2,2'-oxiran]-1-one C14H22O2 ÏàËÆ¶È:57.1% Chemistry & Biodiversity 2010 7 421-439 Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry Andres Parra, Pilar E. Lopez and Andres Garcia-Granados Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . (1R,2R,4aS,8aS)-Octahydro-5,5,8a-trimethyl-1H-spiro[naphthalene-2,2'-oxiran]-1-ol C14H24O2 ÏàËÆ¶È:57.1% Chemistry & Biodiversity 2010 7 421-439 Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry Andres Parra, Pilar E. Lopez and Andres Garcia-Granados Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . (1R,2S,4aS,8aS)-octahydro-5,5,8a-trimethyl-1H-spiro[naphthalene-2,2'-oxiran]-1-ol C14H24O2 ÏàËÆ¶È:57.1% Chemistry & Biodiversity 2010 7 421-439 Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry Andres Parra, Pilar E. Lopez and Andres Garcia-Granados Structure 13C NMR ̼Æ×Ä£Äâͼ |
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