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icaszzx: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-11 11:05:00
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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