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bxzc123

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Based on these facts,Yan et al. [31] reported the microbial transformation of 3-hydroxy-5,6-cyclopropanocholestanes-an alter route to 6-methylsteroids.
Incubation of 3b-hydroxy-5, 6 a -cyclopropano-5 a -cholestane (6)with Mycobacterium sp. (NRRL B-3805) gave three metabolites, 5,6 a -cyclopropano-5 a -androsta-3, 17-dione (7), 3b-hydroxy-5,6 a -cyclopropano-5 a -androsta-17-one (8) and androsta-4-ene-3,17-dione (5). Fermentation of 3b-hydroxy-5, 6b-cyclopropano-5b-
cholestane (9) with Mycobacterium sp. afforded the metabolite 5,5, 6b-cyclopropano-5b-androsta-3, 17-dione (10) and 3 a -hydroxy-5, 6b-cyclopropano-5b-androsta-17-one (11). Similarly, incubationof 3b-hydroxy-5, 6 a -cyclopropano-5 a -cholest-7-ene (12) with Mycobacterium sp. yielded a mixture of side chain cleaved 17-keto steroids as the major products, viz. the cyclopropyl eliminated product 5, 5, 6 a -cyclopropano-5 a -androst-7-ene-3, 17-dione (13),
3b-hydroxy-5, 6 a -cyclopropano-5 a -androst-4-ene-17-one (14), 5,
6 a -cyclopropano-5 a -androst-8(14)-ene-3, 7, 17-trione (15), 5,
6 a -cyclopropano-5 a -androst-8-ene-3, 7, 17-trione (16) and 6 a ,
7 a -cyclopropanoandrost-4-ene-3, 17-dione (17) as described in
Scheme 2.
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ssssllllnnnn

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bxzc123: ½ð±Ò+100, ·­ÒëEPI+1, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-23 21:21:54
Based on these facts,Yan et al. [31] reported the microbial transformation of 3-hydroxy-5,6-cyclo propano cholestane-an alter route to 6-methyl steroids. Incubation of 3¦Â-hydroxy-5, 6 ¦Á-cyclo propano-5 ¦Á-cholestane (6)with Mycobacterium sp. (NRRL B-3805) gave three metabolites, 5,6 ¦Á-cyclo propano-5 ¦Á-androsta-3, 17-dione (7), 3¦Â-hydroxy-5,6 ¦Á-cyclo propano-5 ¦Á-androsta-17-one (8) and androsta-4-ene-3,17-dione (5). Fermentation of 3¦Â-hydroxy-5, 6¦Â-cyclo propano-5¦Â-cholestane (9) with Mycobacterium sp. afforded the metabolite 5,5, 6¦Â-cyclo propano-5¦Â-androsta-3, 17-dione (10) and 3 ¦Á-hydroxy-5, 6¦Â-cyclo propano-5¦Â-androsta-17-one (11). Similarly, incubation of 3¦Â-hydroxy-5, 6 ¦Á-cyclo propano-5 ¦Á-cholest-7-ene (12) with Mycobacterium sp. yielded a mixture of side chain cleaved 17-keto steroids as the major products, viz. the cyclopropyl eliminated product 5, 5, 6 ¦Á-cyclo propano-5 ¦Á-androst-7-ene-3, 17-dione (13), 3¦Â-hydroxy-5, 6¦Á-cyclo propano-5¦Á-androst-4-ene-17-one (14), 5, 6 ¦Á-cyclo propano-5 ¦Á-androst-8(14)-ene-3, 7, 17-trione (15), 5, 6 ¦Á-cyclo propano-5 ¦Á-androst-8-ene-3, 7, 17-trione (16) and 6¦Á, 7¦Á-cyclo propano androst-4-ene-3,17-dione (17) as described in Scheme 2.

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2Â¥2015-04-22 21:25:07
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bxzc123

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ÒýÓûØÌû:
2Â¥: Originally posted by ssssllllnnnn at 2015-04-22 21:25:07
Based on these facts,Yan et al.  reported the microbial transformation of 3-hydroxy-5,6-cyclo propano cholestane-an alter route to 6-methyl steroids. Incubation of 3¦Â-hydroxy-5, 6 ¦Á-cyclo propano-5 ...

The fermentation yielded one reduced product: 17¦Â-hydroxyandrost-1,4-dien-3-one and two hydroxylated
metabolites: 11¦Á-hydroxyandrost-1,4-diene-3,17-dione and 12¦Â-hydroxyandrost-1,4-diene-3,17-dione.Ôõô½âÊÍÇó°ïæ
3Â¥2015-04-23 21:22:41
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