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20.11,20.32,21.30,21.84,23.21,23.49,25.34,25.57,26.86,26.90,26.96,27.11,35.22,36.02,38.11,38.30,41.78,44.78,44.84,52.02,52.06,72.41,72.69,75.48,76.05,124.94,125.32,146.51
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shooter652: ½ð±Ò+8, ¡ïÓаïÖú 2014-06-17 10:17:29
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1 .     (20R,22R)-20,22,25-trihydroxy-2 ¦Â,3 ¦Â-(isopropylidenedioxy)-5¦Â-cholest-8(14)-en-6-one
    ÏàËÆ¶È:66.6%
Russian Journal of Organic Chemistry          2010          46          1735-1740
¦¤8(14)-14¦Á-deoxy- and 14¦Á-deoxy-14¦Á-hydroperoxyecdysteroids
A. Sh. Ibragimova, N. A. Ves¡¯kina, I. V. Galyautdinov and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     cumingianol A
C32H54O6     ÏàËÆ¶È:65.6%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Á,12¦Á,16¦Â-Trihydroxy-5¦Â-cholan-24-oic acid
C24H40O5     ÏàËÆ¶È:64.2%
Steroids          2010          75          506-512
Synthesis, aggregation behavior and cholesterol solubilization studies of 16-epi-pythocholic acid (3¦Á,12¦Á,16¦Â-trihydroxy-5¦Â-cholan-24-oic acid)
Nonappa, Uday Maitra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3,20,24,25-tetrahydroxydammarane
C30H54O4     ÏàËÆ¶È:63.3%
Phytochemistry          2004          65          2173-2176
Insect antifeedant compounds from Nothofagus dombeyi and N. pumilio
Odile Thoison, Thierry S¨¦venet, Hermann M. Niemeyer, Graeme B. Russell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     panicualtin D
C32H52O7     ÏàËÆ¶È:63.3%
Journal of the Indian Chemical Society          1999          76          575-581
Study of the stereochemistry of new tetranortriterpenoids isolated from root-wood of Chisocheton paniculatus Hiern(Meliaceae)
R.D.Yadav,J.C.S.Kataky and R.K.Mathur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Cumingianol B
C32H54O6     ÏàËÆ¶È:62.5%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Cumingianol C
C32H52O5     ÏàËÆ¶È:62.5%
Phytochemistry          2011          72          2205-2211
Triterpenes and a triterpene glucoside from Dysoxylum cumingianum
Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     paniculatin-D
C32H52O7     ÏàËÆ¶È:62.5%
Indian Journal of Chemistry Section B          1999          38B          1359-1363
New protolimonoids and limonoidsart I-isolation,structure elucidation of new protolimonoids and limonoid from the root wood of Chisocheton paniculatus Hiern(Meliaceae)
R D Yadav, J C S Kataky&R K mathur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Kadpolysperin C
C32H50O5     ÏàËÆ¶È:62.5%
Tetrahedron          2012          68          4820-4829
Kadpolysperins A¨CN, lanostane triterpene acids possessing rich structure types from Kadsura polysperma
Ke Dong, Jian-Xin Pu, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Wei Zhao, Yan Li, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     sugikurojin C
C40H56O4     ÏàËÆ¶È:62.0%
Chemical & Pharmaceutical Bulletin          2004          52(3)          354-358
A New Abietane and Two Dimeric Abietane Diterpenes from the Black Heartwood of Cryptomeria japonica
Shigenobu ARIHARA,Akemi UMEYAMA, Shinya BANDO, Shinji IMOTO, Mikako ONO, Mayo TANI, and Kazuko YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     agladupol A
C31H52O6     ÏàËÆ¶È:61.2%
Journal of Natural Products          2007          70          1532-1535
Agladupols A¨CE, Triterpenoids from Aglaia duperreana
Bo-Jun Xie, Sheng-Ping Yang, Hua-Dong Chen, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     petuniosterol B
C28H48O7     ÏàËÆ¶È:60.7%
Phytochemistry          1994          36          1307-1314
Ergostane glycosides from Petunia hybrida
Kazushi Shingu, Hiroshi Fujii, Kouichi Mizuki, Ikuhiko Ueda, Shoji Yahara, Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     1¦Â,3¦Á,11¦Á,20-Tetraacetoxy-5¦Â-pregnane
C29H44O8     ÏàËÆ¶È:60.7%
Steroids          2011          76          1458-1464
Microwave assisted preparation of C(1)-C(11) oxygen-bridged pregnanes
Lautaro D. Alvarez, Juan M. Sonego, Adriana S. Veleiro, Gerardo Burton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 10
    ÏàËÆ¶È:60.7%
Steroids          1990          55          263-265
Studies of the synthesis of biomarkers. VII. Synthesis of 5¦Á-(17R,20R)-14,15-secocholestane
Tong-Shuang Li, Yu-Lin Li, Xiao-Tian Liangt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound IV
    ÏàËÆ¶È:60.7%
Tetrahedron          1995          51          2009-2022
Structure determination of diacholestanes. Their geochemical significance
Odette Sieskind, Jean P. Kintzinger, Bernard Metz, Pierre Albrecht
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (¡À)-(1R*,9S*,10R*,11S*)-and (¡À)-(1R*,9R*,10S*,11R*)-10-hydroxy-12-methyl-1-nitrobicyclo[7.3.1]tridecan-13-one
    ÏàËÆ¶È:60.7%
European Journal of Organic Chemistry          2011                   2101-2110
A General, Diastereoselective Synthesis of Highly Functionalized Bicyclo[n.3.1]alkane Systems Based on an Anionic Domino Reaction of -Nitrocycloalkanones
Giorgio Giorgi, Sonia Miranda, Miriam Ruiz, Jean Rodriguez, Pilar L¨®pez-Alvarado and J. Carlos Men¨¦ndez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     sandorinic acid A
C30H46O5     ÏàËÆ¶È:60%
Journal of Natural Products          2001          64          1243-1245
New Multiflorane-Type Triterpenoid Acids from Sandoricum indicum
Tadamitsu Tanaka,Takashi Koyano, Thaworn Kowithayakorn, Haruhiro Fujimoto, Emi Okuyama,Masahiko Hayashi,Kanki Komiyama, and Masami Ishibashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Mesendanin Q
C30H48O5     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2012          95          286-300
Triterpenoids from Melia toosendan
Shi-Hui Dong, Xiu-Feng He, Lei Dong, Yan Wu, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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