Absolute configurations of enantiomeric K-region cis-5,6-dihydrodiols of 12-methylbenz[A] anthracene and 7-bromo-12-methylbenz[A] anthracene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Exciton chirality method and its application to configurational and conformational studies of natural products
2. The effect of the bay-region 12-methyl group on the stereoselective metabolism at the K-region of 7,12-dimethylbenz[a]anthracene by rat liver microsomes
3. Stereoselective metabolism of 6-bromobenzo[a]pyrene by rat liver microsomes: Absolute configuration of trans-dihydrodiol metabolites
4. Stereoselective metabolism of 7-bromobenz [a]anthracene by rat liver microsomes: absolute configurations of trans-dihydrodiol metabolites
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Solvolysis of K-region arene oxides: substituent effects on reactions of benz[a]anthracene 5,6-oxide;Journal of the American Chemical Society;1991-05
2. Absolute configuration ofcis-5,6-dihydrodiol enantiomers derived from helical conformers of 1,12-dimethylbenz[a]anthracene;Chirality;1990
3. Stereoselectivity of cytochrome P-450 isozymes and epoxide hydrolase in the metabolism of polycyclic aromatic hydrocarbons;Biochemical Pharmacology;1988-01
4. The Use of Pirkle High-Performance Liquid Chromatography Phases in the Resolution of Enantiomers of Polycyclic Aromatic Hydrocarbon Metabolites;Chiral Separations;1988
5. Stereoselective formation and hydration of 12-methylbenz[a]anthracene 5,6-epoxide enantiomers by rat liver microsomal enzymes;Biochemical Journal;1987-07-01
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