The Allylic Oxidation of Geraniol Catalyzed by Cytochrome P‐450Cath., Proceeding with retention of configuration
- 15 March 1989
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 72 (2) , 391-400
- https://doi.org/10.1002/hlca.19890720227
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Regioselectivity and Deuterium Isotope Effects in Geraniol Hydroxylation by the Cytochrome P‐450 Monooxygenase from Catharanthus roseus (L.) G. DONHelvetica Chimica Acta, 1986
- The stereochemistry of the incorporation of the methyl groups of ‘chiral methyl valine’ into methylene groups in cephalosporin CJournal of the Chemical Society, Chemical Communications, 1983
- Application of tritium NMR spectroscopy in the determination of the stereochemistry of dehydrogenation of isobutyryl CoA in Pseudomonas putidaJournal of the American Chemical Society, 1980
- Chiral Methyl GroupsPublished by Wiley ,1979
- Stereochemistry of the 1,3-proton loss from a chiral methyl group in the biosynthesis of cycloartenol as determined by tritium nuclear magnetic resonance spectroscopyJournal of the American Chemical Society, 1978
- Determination of the enantiomeric purity and absolute configuration of α-deuteriated primary alcoholsJournal of the Chemical Society, Chemical Communications, 1973
- Preparation of Carboxylic Esters and Phosphoric Esters by the Activation of AlcoholsBulletin of the Chemical Society of Japan, 1971
- Synthesis and Configurational Assay of Asymmetric Methyl GroupsEuropean Journal of Biochemistry, 1970
- Asymmetric Methyl Groups: Preparation and Detection of Chiral Methyl GroupsNature, 1969
- Asymmetric Methyl Groups: Asymmetric Methyl Groups, and the Mechanism of Malate SynthaseNature, 1969