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wj_2000_abc(wangkaibo123´ú·¢): ½ð±Ò+15 2015-03-26 14:55:47
1 .     codonopilate A
C49H82O3     ÏàËÆ¶È:66.6%
Journal of Natural Medicines          2011          65          18-23
Three new triterpenyl esters, codonopilates A¨CC, isolated from Codonopsis pilosula
Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     codonopilate B
C49H82O3     ÏàËÆ¶È:64.7%
Journal of Natural Medicines          2011          65          18-23
Three new triterpenyl esters, codonopilates A¨CC, isolated from Codonopsis pilosula
Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     codonopilate C
C49H80O3     ÏàËÆ¶È:62.7%
Journal of Natural Medicines          2011          65          18-23
Three new triterpenyl esters, codonopilates A¨CC, isolated from Codonopsis pilosula
Daigo Wakana ,Nobuo Kawahara ,Yukihiro Goda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     29-norcycloart-5-ene and 5,8-lanostadiene-3¦Â-ol
    ÏàËÆ¶È:61.5%
Zeitschrift f¨¹r Naturforschung C          2004          59          15-18
Chemical Constituents of Euphorbia marschalliana Boiss.
A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     mixture of compound 13A and compound 13B
C30H46O4     ÏàËÆ¶È:60.7%
Tetrahedron          2002          58          8073-8086
Cytotoxic and anti-HIV-1 constituents of Gardenia obtusifolia and their modified compounds
Patoomratana Tuchinda, Wilart Pompimon, Vichai Reutrakul, Manat Pohmakotr, Chalobon Yoosook, Natedao Kongyai, Samaisukh Sophasan, Kulawee Sujarit, Suchart E Upathum, Thawatchai Santisuk
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     mixture of compound 13A and compound 13B
C30H44O4     ÏàËÆ¶È:60.7%
Tetrahedron          2002          58          8073-8086
Cytotoxic and anti-HIV-1 constituents of Gardenia obtusifolia and their modified compounds
Patoomratana Tuchinda, Wilart Pompimon, Vichai Reutrakul, Manat Pohmakotr, Chalobon Yoosook, Natedao Kongyai, Samaisukh Sophasan, Kulawee Sujarit, Suchart E Upathum, Thawatchai Santisuk
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Methyl 4-(methoxyimino)-5¦Â-cholan-24-oate
C26H43NO3     ÏàËÆ¶È:60.7%
Russian Journal of Organic Chemistry          2014          50          1044¨C1047
First Synthesis of Steroidal 1,2,4-Trioxolanes
E. Yu. Yamansarov, O. B. Kazakova, N. I. Medvedeva, D. V. Kazakov, O. S. Kukovinets, and G. A. Tolstikov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     compound 7
    ÏàËÆ¶È:56.8%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     Sinocalycanchinensin C
C49H82O4     ÏàËÆ¶È:56.8%
Bioorganic & Medicinal Chemistry          2011          19          2790-2796
New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis
Yoshiki Kashiwada , Kazuya Nishimura, Shin-ichiro Kurimoto, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     cycloeucalenol linolenate
C48H78O2     ÏàËÆ¶È:56.8%
Chemical & Pharmaceutical Bulletin          2009          57          401-404
Alpha-Reductase and Aromatase Inhibitory Constituents from Brassica rapa L. Pollen
Yong-Hui Li, Yi-Fang Yang, Kun Li, Li-Li Jin, Nian-Yun Yang and De-Yun Kong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     cycloeucalenol vernolitate
C48H80O3     ÏàËÆ¶È:56.8%
Journal of the Chinese Chemical Society          2000          47          555-560
The Chemical Constituents from the Heartwood of Eucalyptus citriodora
Ching-Kuo Lee* and Ming-Huey Chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     Methyl 4a,9a-(trans)-4,4,8,9a-tetramethyl-2,3,4,4a,5,6,7/9,9aoctahydro-1H-benzo[7] annulene-6-carboxylate
    ÏàËÆ¶È:56.8%
Flavour and Fragrance Journal          2014          29          59−66
Preparation and olfactory evaluation of mono- and bicyclic compounds featuring gem-dimethylcyclohexane structures
Julien Godeau, Fanny Grau, Sylvain Antoniotti* and Elisabet Duñach
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     cycloartenyl esters
    ÏàËÆ¶È:56.3%
Chemical & Pharmaceutical Bulletin          2004          52          1382-1384
Chemical Constituents of Malagasy Liverworts, Part II: Mastigophoric Acid Methyl Ester of Biogenetic Interest from Mastigophora diclados (Lepicoleaceae Subf. Mastigophoroideae)
Liva Harinantenaina and Yoshinori Asakawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     (1R,3aR,4RS,5S,7aR)-1-((R)-1,5-dimethylhexyl)-5-(2,3-dimethylphenylamino)-3a,7a-dimethyl-octahydroinden-4-ol
    ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2013          21          1925-1943
Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase
Mathias König, Christoph M¨¹ller, Franz Bracher
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     fraction a
    ÏàËÆ¶È:54.9%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     compound 9
C60H987O2     ÏàËÆ¶È:54.9%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     pseudolaridimer A
C50H78O5     ÏàËÆ¶È:54.9%
Organic Letters          2012          14          5432-5435
Pseudolaridimers A and B, Hetero-Cycloartane¨CLabdane Diels¨CAlder Adducts from the Cone of Pseudolarix amabilis
Bo Li, De-Yun Kong, Yun-Heng Shen, Hu Yuan, Rong-Cai Yue, Yi-Ren He, Lu Lu, Lei Shan, Hui-Liang Li, Ji Ye, Xian-Wen Yang, Juan Su, Run-Hui Liu, and Wei-Dong Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     (R)-2-((R)-1-acetoxy-17-{(1S,2R)-2-[(1S,20S,21S)-20-(tetrahydro-2H-pyran-2-yl)-1,21-dimethyl-nonatriacontyl]cyclopropyl}heptadecyl)hexacosnoic acid methyl ester
C95H184O6     ÏàËÆ¶È:54.9%
Tetrahedron          2013          69          6285-6296
The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes
Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     compound 6
    ÏàËÆ¶È:52.9%
Chemical & Pharmaceutical Bulletin          1992          40          1773-1778
Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei
Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     N-[3-oxolup-20(29)-en-28-oyl]-D,L-¦Á-aminopropionic acid
C34H53NO4     ÏàËÆ¶È:52.9%
Chemistry of Natural Compounds          2008          44          327-333
SYNTHESIS OF BETULONIC ACID AMIDES
A. N. Antimonova, N. V. Uzenkova, N. I. Petrenko,M. M. Shakirov, E. E. Shul¡äts, and G. A. Tolstikov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     prosapogenin methyl ester
    ÏàËÆ¶È:52.9%
Phytochemistry          1995          38          939-942
Cycloartane-type glycosides from Thalictri Herba
Hitoshi Yoshimitsu, Kazuhiro Hayashi, Miki Kumabe, Toshihiro Nohara
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