Enantioselectivity in the Rabbit Liver Microsomal Biotransformation of Styrene and Phenylpropenes
Author:
Affiliation:
1. Dipartimento di Chimica Bioorganica, via Bonanno 33, 56126, Pisa, Italy
Publisher
Informa UK Limited
Subject
General Agricultural and Biological Sciences,Biochemistry,Biotechnology,Catalysis
Link
https://www.tandfonline.com/doi/pdf/10.3109/10242429409065225
Reference23 articles.
1. Substrate enantioselectivity m the rabbit liver microsomal epoxide hydrolase catalyzed hydrolysis of trans and cis 1-phenylpropene oxides. A comparison with styrene oxide
2. The cytochrome P-450 catalyzed oxidation of 1-methylcyclohexene. Competition between hydroxylation and epoxidation and absolute stereochemistry of the epoxidation
3. Calculated and experimental absolute stereochemistry of the styrene and .beta.-methylstyrene epoxides formed by cytochrome P 450cam
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