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1 . (4E)-jatrogrossidentadione acetate C22H30O5 ÏàËÆ¶È:59.0% Phytochemistry 2008 69 2639-2641 Diterpenoids from Jatropha multifida Biswanath Das, Bommena Ravikanth, Kongara Ravinder Reddy, Ponnaboina Thirupathi,Tuniki Venugopal Raju, Balasubramanian Sridhar Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1¦Á-acetoxy-6¦Â-(2¦Î-methylbutyryloxy)-10¦ÁH-9-oxofuranoeremophilane C22H30O6 ÏàËÆ¶È:59.0% Journal of Natural Products 2004 67 1483-1487 Constituents of Senecio chionophilus with Potential Antitubercular Activity Jian-Qiao Gu, Yuehong Wang, Scott G. Franzblau, Gloria Montenegro, and Barbara N. Timmermann Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 11R-Acetoxyhalima-5,13E-dien-15-oic acid C22H34O4 ÏàËÆ¶È:59.0% Biochemical Systematics and Ecology 2007 35 215-221 Further diterpenoids from Plectranthus ornatus and P. grandidentatus Patricia Rijo, Cristina Gaspar-Marques, Mar¨ªa F. Simões, Mar¨ªa L. Jimeno, Benjam¨ªn Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . triptogelin G-2 C24H32O5 ÏàËÆ¶È:59.0% Phytochemistry 1992 31 3943-3947 Sesquiterpene esters from Tripterygium wilfordii Yoshihisa Takaishi, Fumie Aihara, Shouji Tamai, Kimiko Nakano, Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . epoxicorcovadin acetate C22H30O4 ÏàËÆ¶È:59.0% Tetrahedron letters 1983 24 5043-5046 Two new diterpenes with a rosane skeleton from velloziaceae. Angelo C. Pinto, Tereza Cristina V. Scofield, Raimundo Braz Filho Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (3S*,4R*,7S*,8S*,11S*,13S*)-8-isocyanoamphilecta-1(12),14-diene C21H31N ÏàËÆ¶È:57.1% Journal of Natural Products 2004 67 833-837 Terpene Isocyanides, Isocyanates, and Isothiocyanates from the Okinawan Marine Sponge Stylissa sp. Hidemichi Mitome, Nao Shirato, Hiroaki Miyaoka, Yasuji Yamada, and Rob W. M. van Soest Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-hydroxyandrost-4-en-17-one C19H28O2 ÏàËÆ¶È:57.1% Natural Product Research 2000 14 217-224 Fungal Transformations of Steroids by Cephalosporium Aphidicola and Trichothecium Roseum Atta-Ur-Rahman; M. Iqbal Choudhary; Fahim Asif; Afgan Farooq; M. Yaqoob Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . l¦Á-acetoxy-6¦Â-isobutyroxy-9-oxo-l0¦ÁH-furanoeremophilane ÏàËÆ¶È:57.1% Journal of Natural Products 1991 Vol 54 588 9-Oxo-10¦ÁH-furanoeremophilanes from Senecio chilensis and Senecio patagonicus Luis Villarroel, Ren¨¦ Torres, Jos¨¦ Gavin, Mat¨ªas Reina, Gabriel de la Fuente Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . pernetyl malonate C18H28O5 ÏàËÆ¶È:57.1% Phytochemistry 1994 35 425-433 The sesquiterpenes of Fabiana imbricata Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Valerianin B C17H24O4 ÏàËÆ¶È:57.1% Fitoterapia 2012 83 599-603 In vivo antidepressant activity of sesquiterpenes from the roots of Valeriana fauriei Briq Xue Gui Liu, Pin Yi Gao, Guo Sheng Wang, Shao Jiang Song, Ling Zhi Li, Xi Li,Xin Sheng Yao, Zhen Xue Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . dihydrotucumanoic acid ÏàËÆ¶È:57.1% Phytochemistry 1987 26 3281-3283 Neo-clerodane diterpenoids and other constituents from Baccharis species Francesca Faini,Patricio Rivera,Manuel Mah¨²,Mariano Castillo Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 14 C21H32O2 ÏàËÆ¶È:57.1% Tetrahedron 2012 68 1729-1735 Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A Arata Yajima, Yuuma Kagohara, Keisuke Shikai, Ryo Katsuta, Tomoo Nukada Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 6¦Á-acetoxy-8¦Â,13;13,17-diepoxy-14,15-bisnorlabdane C20H32O4 ÏàËÆ¶È:57.1% Tetrahedron 2006 62 8489-8497 Photodegradation of some 14,15-bisnorlabdene-13-ones, derived from larixol. Synthesis of drimanic dienes with functional groups at C-6 Pavel F. Vlad, Alexandru G. Ciocarlan, Mihai N. Coltsa, Calin Deleanu, Oana Costan, Yurii A. Simonov, Victor Ch. Kravtsov, Janusz Lipkowski, Tadeusz Lis, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 17 C28H50O3Si ÏàËÆ¶È:57.1% Journal of the American Chemical Society 2003 125 1498-1500 Total Synthesis of Ingenol Keiji Tanino, Kei Onuki, Kohei Asano, Masaaki Miyashita, Tsuyoshi Nakamura, Yoshinori Takahashi, and Isao Kuwajima Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (13S,14S)-14,17-Diacetoxy-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstan-17-one 17-oxime ÏàËÆ¶È:54.5% Steroids 2004 69 511-514 Reaction of (13S)-13-iodo-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstane-14,17-dione with hydroxylamine and its application to the synthesis of new 13,14-seco steroids Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Galina P. Fando, Yuliya Y. Zhiburtovich, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2-Acetyl ent-dihydrotucumanoic acid ÏàËÆ¶È:54.5% Phytochemistry 1994 35 1505-1507 Ent-neoclerodane diterpenes from Gymnosperma glutinosum Roberto Mart¨ªnez, Jos¨¦ S. Calder¨®n, Rub¨¦n A. Toscano, Luc¨ªa Valle-Aguilera, H¨¦ctor M. Mendoza-Candelaria Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (1S*,3E,5R*,7E,11S*,12S*)-5-acetoxy-12-hydroxydrolabella-3,7-dien-9-one C22H34O4 ÏàËÆ¶È:54.5% Phytochemistry 1994 37 509-513 Diterpenes from the brown alga Dictyota bartayresiana Ch.Bheemasankara Rao, G. Trimurtulu, Ch. Sreedhara, D.Venkata Rao, Steven C. Bobzin, D.John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Klysimplexin X C22H38O6 ÏàËÆ¶È:54.5% Bulletin of the Chemical Society of Japan 2011 84 1237-1242 Klysimplexins U¨CX, Eunicellin-Based Diterpenoids from the Cultured Soft Coral Klyxum simplex Bo-Wei Chen, Chiung-Yao Huang, Zhi-Hong Wen, Jui-Hsin Su, Wei-Hsien Wang, Ping-Jyun Sung, Yang-Chang Wu, Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 15,16-diacetoxy-15,16-4,18-diepoxy-ent-cleroda-12Z-diene C24H26O6 ÏàËÆ¶È:54.5% Tetrahedron 1993 49 9067-9078 Neo-clerodane diterpenoids from aerial parts of linaria saxatilis var. glutinosa Arturo San Feliciano, Marina Gordaliza, Jos¨¦ M. Miguel del Corral, Mar¨ªa L. de la Puente, Santiago Garc¨ªa-Granda, Miguel A. Salvado Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 16 C22H34O3 ÏàËÆ¶È:54.5% Tetrahedron 1987 43 2999-3007 A new class of monocyclic diterpenes from eremophila foliosissima kraenzlin. (Myoporaceae) P.G. Forster, E.L. Ghisalberti, P.R. Jefferies Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 2-Methyl-5¦Á-androst-2-en-17¦Â-yl acetate C22H34O2 ÏàËÆ¶È:54.5% Organic Magnetic Resonance 1977 9 439-464 13C n.m.r. spectra of steroids ¡ªa survey and commentary J. W. Blunt and J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3-Methyl-5¦Á-androst-2-en-17¦Â-yl acetate C22H34O2 ÏàËÆ¶È:54.5% Organic Magnetic Resonance 1977 9 439-464 13C n.m.r. spectra of steroids ¡ªa survey and commentary J. W. Blunt and J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 22 C24H38O5 ÏàËÆ¶È:54.1% European Journal of Organic Chemistry 2011 538-546 Asymmetric Synthesis and in vivo Biological Inactivity of the Right-Hand Terpenoid Fragment of Terpendole E Masato Oikawa, Ryo Hashimoto and Makoto Sasaki Structure 13C NMR ̼Æ×Ä£Äâͼ |

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