Hydroxylation of camphor and pericyclocamphanone. Evidence against substrate binding through enol linkages
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference8 articles.
1. Product Formation from Ferrous Oxy-Cytochrome P-450
2. Camphor binding by Pseudomonas putida cytochrome P-450
3. Biological Hydroxylation Mechanisms;Estabrook,1972
4. The log kexovs. log kendo correlation as a mechanistic criterion; on the mechanisms of solvolysis of norbornyl derivatives and base-catalyzed isotope exchange of norbornanones
5. Towards a complete account of the exchange chemistry of a diastereotopic proton pair. I. Base-catalyzed enolization–exchange of 2-norbornanones; on the rate controlling factors
Cited by 4 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. Microbiological Asymmetric Hydroxylation of 7-Carboxybicyclo[2.2.1]heptane and hept-2-ene and Their Methyl Esters Giving Potentially Useful Chiral Synthons for Cyclopentanoids;Agricultural and Biological Chemistry;1985-11
2. Structure and Chemistry of Cytochrome P-450;Metalloproteins;1985
3. Identification of elimination reactions during the degradation of 5-bromocamphor by P. Putida;Biochemical and Biophysical Research Communications;1980-05
4. Oxidases and reductases;Inorganic Biochemistry
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