由6α-和6β-苯氧基乙酰氨基青霉素酸甲酯形成对映体4-氧杂-2,6-二氮杂双环(3.2.0)庚-2-烯-7-酮。 - Suppr | 超能文献

Formation of enantiomeric 4-oxa-2,6-diazabicyclo(3.2.0)hept-2-en-7-ones from methyl 6alpha- and 6beta-phenoxyacetamidopenicillanates.

作者信息

Campbell M M, Johnson G

出版信息

J Chem Soc Perkin 1. 1975(19):1932-4.

Abstract

摘要

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Formation of enantiomeric 4-oxa-2,6-diazabicyclo(3.2.0)hept-2-en-7-ones from methyl 6alpha- and 6beta-phenoxyacetamidopenicillanates.由6α-和6β-苯氧基乙酰氨基青霉素酸甲酯形成对映体4-氧杂-2,6-二氮杂双环(3.2.0)庚-2-烯-7-酮。

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2

Studies related to penicillins. Part XVI. Preparation of methyl 2-((1S,5R)-3-benzyl-7-oxo-4-oxa-2,6-diazabicyclo(3.2.0)hept-2-en-6-yl)-3-methylbut-2-enoate.与青霉素相关的研究。第十六部分。2-((1S,5R)-3-苄基-7-氧代-4-氧杂-2,6-二氮杂双环(3.2.0)庚-2-烯-6-基)-3-甲基-2-丁烯酸甲酯的制备。

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3

Synthesis and analgesic activity of 5-aryl-3-azabicyclo [3.2.0.] heptan-6-one dimethylacetals: compounds with extraordinary morphine-like properties.5-芳基-3-氮杂双环[3.2.0]庚-6-酮二甲基缩醛的合成与镇痛活性：具有非凡吗啡样性质的化合物

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6

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7

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8

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9

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