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1 . 11¦Á-angeloyloxy-1¦Á-hydroxy-3-oxo-6¦ÁH,7¦ÁH,10¦ÁMe-eudesm-4-en-6,12-olide C20H26O6 ÏàËÆ¶È:61.1% Phytochemistry 1997 45 1645-1651 Sesquiterpenolides from Melanoselinum decipiens Guillermo M. Massanet, Francisco M. Guerra, Zacar¨ªas D. Jorge, Carmen Astorga Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 11¦Á,13-dihydroalantolactone C15H22O2 ÏàËÆ¶È:60% Journal of Natural Products 2001 64 466-471 Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 7-drimen-9¦Á,11,12-triol C15H26O3 ÏàËÆ¶È:60% Journal of Natural Products 1999 62 1488-1491 Synthesis of 11, 12-Epoxydrim-8, 12-en-11-ol, 11, 12-Diacetoxydrimane, and Warburganal from (-)-Sclareol A. F. Barrero, M. Cort¨¦s, E. A. Manzaneda, E. Cabrera, R. Chahboun, M. Lara, and A. R. Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 10 C15H20O4 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2006 8 317-330 Biotransformation of a- and 10b-santonin by fungus and plant cell cultures L. YANG, J. DAI, J.-I. SAKAI and M. ANDO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 6 C15H24O4 ÏàËÆ¶È:60% Acta Pharmaceutica Sinica 2005 Vol 40 834-837 Biotransformation of 6¦Â-santonin by Phytolacca acinosa cell suspension cultures YANG Lin; DAI Jun-gui Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (3R,3¦ÁR,4¦ÁS,7¦ÁS,8S,9¦ÁS)-3,4¦Á,8-trimethyldecahydroazuleno[6,5-¦Â]furan-2,5-dione C15H22O3 ÏàËÆ¶È:60% Natural Product Research and Development 2010 22 736-739 Sesquiterpenoids from Tibetan Folk Drug Pulicaria insignis HUANG Sheng-zhuo;JIANG Si-ping; ZHU Hua-jie Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 9¦Â-hydroxy-3-oxo-6,7¦ÁH,11¦ÂH-eudesm-4-en-6,12-olide ÏàËÆ¶È:60% Tetrahedron 1995 51 5609-5616 Synthesis of 9-oxyfunctionalized eudesmanes from artemisin Victoria Bargues, Gonzalo Blay, Bego?a Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 7a ÏàËÆ¶È:56.2% Tetrahedron 1995 51 5609-5616 Synthesis of 9-oxyfunctionalized eudesmanes from artemisin Victoria Bargues, Gonzalo Blay, Bego?a Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (5¦Â ,6¦Á )-6,11-dihydroxyeudesmane C15H28O2 ÏàËÆ¶È:53.3% Chemistry & Biodiversity 2006 Vol. 3 337 New Chemical Constituents from the Endophyte Streptomyces Species LR4614 Cultivated on Maytenus hookeri Pei-Ji Zhao, Guo-Hong Li, and Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 5-epidilatanolide ÏàËÆ¶È:53.3% Phytochemistry 2002 59 205-213 Eremophilanolides and other constituents from the Argentine liverwort Frullania brasiliensis Alicia Bard¨®n, Graciela Bovi Mitre, Norma Kamiya, Masao Toyota,Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2R,11-dihydroxy-1(10)-tremulen-5,12-olide C15H22O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2008 71(8) 1423-1426 Sesquiterpenes and Aliphatic Diketones from Cultures of the Basidiomycete Conocybe siliginea Zhong-Yu Zhou, Jian-Guo Tang, Fei Wang, Ze-Jun Dong, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 7-drimen-9¦Á,11-diol C15H26O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 1488-1491 Synthesis of 11, 12-Epoxydrim-8, 12-en-11-ol, 11, 12-Diacetoxydrimane, and Warburganal from (-)-Sclareol A. F. Barrero, M. Cort¨¦s, E. A. Manzaneda, E. Cabrera, R. Chahboun, M. Lara, and A. R. Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 15 ÏàËÆ¶È:53.3% Journal of Natural Products 1997 60 1026-1030 Sesquiterpene Glycosides and Phenylpropanoid Esters from Phonus arborescens (Carthamus arborescens) Alejandro F. Barrero, Pilar Arteaga, Jos¨¦F. Qu¨ªlez, Ignacio Rodr¨ªguez, and M. Mar Herrador Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 6-hydroperoxy-5,6-dihydro-4,5-dehydro-epi-antheindurolide A C15H18O6 ÏàËÆ¶È:53.3% Natural Product Research 2008 22 907-914 Irregular linear sesquiterpene dilactones from Anthemis auriculata Boiss. Milka Todorova; Jordanka Staneva; Pavleta Denkova; Ljuba Evstatieva Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 3 ÏàËÆ¶È:53.3% Phytochemistry 1993 32 460-462 Sesquiterpene lactones from Artemisia species J. Alberto Marco, Juan F. Sanz, F. Sancenon, A. Rustaiyan, M. Saberi Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . seiricardine B C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 1993 33 69-78 Seiricardines B and C, phytotoxic sesquiterpenes from three species of Seiridium pathogenic for cypress Antonio Evidente, Andrea Motta, Lorenzo Sparapano Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . eremophila-9,11-dien-8¦Á-ol C15H24O ÏàËÆ¶È:53.3% Phytochemistry 1992 31 4027-4028 (+)-(4S*,5R*,7S*,8R*)-eremophila-9,11-dien-8¦Á-ol from the liverwort Marsupella emarginata Leslie J. Harrison, Hans Becker, Joseph D. Connolly, David S. Rycroft Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . armexifolin ÏàËÆ¶È:53.3% Phytochemistry 1984 23 1665-1668 Sesquiterpene lactones of Artemisia mexicana var. Angustifolia Rachel Mata, Guillermo Delgado, Alfonso Romo de Vivar Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 1(R)-hydroxypolygodial ÏàËÆ¶È:53.3% Tetrahedron Letters 2005 46 4061-4063 Enantioselective synthesis of 1(R)-hydroxypolygodial Carmela Della Monica, Giorgio Della Sala, Deborah D¡¯Urso, Irene Izzo, Aldo Spinella Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (3aR,5aS,7R,9aR,9bR)-3a,5a,6,7,8,9,9a,9b-octahydro-7,9b-dimethylnuphtho[1,2-c]-furan-1(3H)-one C14H20O2 ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 1985 861-863 Metabolic products of Phomopsis oblonga. Part 1. 3a,5a,6,7,8,9,9a,9b-Octahydro-7,9b-dimethylnaphtho[1,2-c]furan-1(3H)-one (oblongolide) Michael J. Begley and John Frederick Grove Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 3¦Â,14¦Â,10¦Á-trihydroxy-1¦Â,6¦Á,7¦Â(H)-cadinane C15H28O3 ÏàËÆ¶È:53.3% Tetrahedron 2000 56 Corrigendum to ¡°Jasonol, a Rare Tricyclic Eudesmane Sesquiterpene and Six other New Sesquiterpenoids from Jasonia candicans¡± Ahmed A Ahmed, Ahmed A Mahmoud Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (5R)-5-isopropyloct-7-en-2-ol C11H22O ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2011 47 1142-1145 Unusual behavior of methylidentriphenylphosphorane in reactions with seven-membered lactols G. Yu. Ishmuratov, V. A. Vydrina, M. P. Yakovleva, E. F. Valeeva and R. R. Muslukhov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 1¦Â-acetoxy-3¦Á-hydroxy-4¦Â,,5¦Á,11¦Â-H-eudesman-6¦Á,12-olide C17H26O5 ÏàËÆ¶È:52.9% Journal of Natural Products 1995 Vol 58 1498-1507 Microbial Transformations of 6¦Á- and 6 ¦Â-Eudesmanolides by Rhizopus nigricans Cultures Yolanda Garc¨ªa, Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . methyl-1¦Â, 10¦Â-epoxy-6¦Á-hydroxy-7(10)-en-8-oxoeremophil-12-oate C16H22O5 ÏàËÆ¶È:50% Planta Medica 1997 63 335-338 New Sesquiterpenes from Two Ligularia Species Hai-Ruo Peng,Yan-Ping Shi, and Zhong-Jian jia Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . methyl-1¦Â,10¦Â-epoxy-7(11)-en-6¦Á-hydroxy-8-oxo-ermophil-12-oate ÏàËÆ¶È:50% Chinese Chemical Letters 1995 6 875-876 NEW SESQUITERPENNE FROM LIGULARIA SAGITTA LI YANG,HAI RUO PENG,ZHONG JIANG JIA Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 4 C16H26O3 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 9019-9022 Stereoselective synthesis of the fully functionalized core fragment of terpentecin Taotao Ling, Fatima Rivas, Emmanuel A. Theodorakis Structure 13C NMR ̼Æ×Ä£Äâͼ |

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