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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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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
2Â¥2015-06-17 09:52:06
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ÕÒÕÒÎÒ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-18 10:43:37
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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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