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13C NMR (100 MHz, CDCl3) ¦Ä13.7,14.0, 14.2, 18.1, 19.1, 22.8, 29.8, 30.7, 32.0, 37.3, 41.0, 43.8, 45.9, 46.1, 52.5, 67.2, 74.9, 171.6, 174.1
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3Â¥: Originally posted by ÇǽðΪ at 2015-06-17 09:52:23
vilmorinine E
C20H24O8     ÏàËÆ¶È:65%
Phytochemistry          1998          48          565-568
Quassinoids from Ailanthus vilmoriniana
Koichi Takeya, Hideyuki Kobata, Akira Ozeki, Hiroshi Mori ...

4Â¥2015-06-18 10:43:40
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
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Ìú¸Ëľ³æ (ÖøÃûдÊÖ)

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²éѯ½á¹û£º¹²²éµ½6¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     vilmorinine E
C20H24O8     ÏàËÆ¶È:65%
Phytochemistry          1998          48          565-568
Quassinoids from Ailanthus vilmoriniana
Koichi Takeya, Hideyuki Kobata, Akira Ozeki, Hiroshi Morita, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Â,5¦Á-dihydroxyandrostan-6,17-dione
C19H24O4     ÏàËÆ¶È:63.1%
Phytochemistry          1993          33          831-834
The biotransformation of some steroids by Cephalosporium aphidicola
James R. Hanson, Habib Nasir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 11
C15H22O3     ÏàËÆ¶È:63.1%
Tetrahedron          1989          45          6297-6308
A new stereochemical class of bicyclic sesquiterpenes from eremophila virgata W.V. Fitzg. (Myoporaceae)
E.L. Ghisalberti, P.R. Jefferies, B.W. Skelton, A.H. White, R.S.F. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4¦Â,7¦Á,17¦Â-trihydroxy-4¦Á,17¦Á-dimethyl-5¦Á-androstane
C21H36O3     ÏàËÆ¶È:61.9%
Phytochemistry          1999          50          25-30
The microbiological hydroxylation of 4¦Â-hydroxy-4¦Á-methyl-5¦Á-androstanes by Cephalosporium aphidicola
Caroline S. Bensasson, Yvan Chevolot, James R. Hanson , Jacques Quinton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     4¦Â,7¦Á-dihydroxy-4¦Á-methyl-5¦Á-androstan-17-one
C20H32O3     ÏàËÆ¶È:60%
Phytochemistry          1999          50          25-30
The microbiological hydroxylation of 4¦Â-hydroxy-4¦Á-methyl-5¦Á-androstanes by Cephalosporium aphidicola
Caroline S. Bensasson, Yvan Chevolot, James R. Hanson , Jacques Quinton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     involucratin
C19H26NO2     ÏàËÆ¶È:60%
Phytochemistry          1989          28          3395-3397
Guaianolides from Saussurea involucrata
Li Yu,Jia Zhong-Jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2015-06-17 09:52:06
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

ÇǽðΪ

гæ (СÓÐÃûÆø)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÕÒÕÒÎÒ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-18 10:43:37
vilmorinine E
C20H24O8     ÏàËÆ¶È:65%
Phytochemistry          1998          48          565-568
Quassinoids from Ailanthus vilmoriniana
Koichi Takeya, Hideyuki Kobata, Akira Ozeki, Hiroshi Morita, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     3¦Â,5¦Á-dihydroxyandrostan-6,17-dione
C19H24O4     ÏàËÆ¶È:63.1%
Phytochemistry          1993          33          831-834
The biotransformation of some steroids by Cephalosporium aphidicola
James R. Hanson, Habib Nasir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     compound 11
C15H22O3     ÏàËÆ¶È:63.1%
Tetrahedron          1989          45          6297-6308
A new stereochemical class of bicyclic sesquiterpenes from eremophila virgata W.V. Fitzg. (Myoporaceae)
E.L. Ghisalberti, P.R. Jefferies, B.W. Skelton, A.H. White, R.S.F. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     4¦Â,7¦Á,17¦Â-trihydroxy-4¦Á,17¦Á-dimethyl-5¦Á-androstane
C21H36O3     ÏàËÆ¶È:61.9%
Phytochemistry          1999          50          25-30
The microbiological hydroxylation of 4¦Â-hydroxy-4¦Á-methyl-5¦Á-androstanes by Cephalosporium aphidicola
Caroline S. Bensasson, Yvan Chevolot, James R. Hanson , Jacques Quinton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     4¦Â,7¦Á-dihydroxy-4¦Á-methyl-5¦Á-androstan-17-one
C20H32O3     ÏàËÆ¶È:60%
Phytochemistry          1999          50          25-30
The microbiological hydroxylation of 4¦Â-hydroxy-4¦Á-methyl-5¦Á-androstanes by Cephalosporium aphidicola
Caroline S. Bensasson, Yvan Chevolot, James R. Hanson , Jacques Quinton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     involucratin
C19H26NO2     ÏàËÆ¶È:60%
Phytochemistry          1989          28          3395-3397
Guaianolides from Saussurea involucrata
Li Yu,Jia Zhong-Jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2015-06-17 09:52:23
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
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