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真菌对8-氯-10,11-二氢二苯并(b,f)(1,4)恶唑嗪的微生物转化

Microbial transformation of 8-chloro-10,11-dihydrodibenz(b,f)(1,4)oxazepine by fungi.

作者信息

Jiu J, Mizuba S, Hribar J

出版信息

Appl Environ Microbiol. 1977 Jan;33(1):26-30. doi: 10.1128/aem.33.1.26-30.1977.

Abstract

The microbial transformation of 8-chloro-10,11-dihydrodibenz(b,f)(1,4)oxazepine (compound I) was undertaken to obtain new derivatives. Compound I was transformed by Hormodendrum sp. (NRRL 8133) to 8-chloro-10,11-dihydrodibenz(b,f)(1,4)oxazepine-11-one (compound II) and 2-(2-amino-4-chlorophenoxy)benzyl alcohol (compound IV). Microbial cleavage of the nonaromatic ring to form compound IV was accomplished by several other fungi. Compound I was transformed to 8-chlorodibenz(b,f)(1,4)oxazepine (compound III) by Hormodendrum cladosporioides (NRRL 8132).

摘要

对8-氯-10,11-二氢二苯并(b,f)(1,4)恶嗪(化合物I)进行微生物转化以获得新的衍生物。化合物I被链格孢属真菌(NRRL 8133)转化为8-氯-10,11-二氢二苯并(b,f)(1,4)恶嗪-11-酮(化合物II)和2-(2-氨基-4-氯苯氧基)苄醇(化合物IV)。非芳环的微生物裂解形成化合物IV是由其他几种真菌完成的。化合物I被枝孢状枝孢菌(NRRL 8132)转化为8-氯二苯并(b,f)(1,4)恶嗪(化合物III)。

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