Some Baeyer–Villiger oxidations using a monooxygenase enzyme from Pseudomonas putida NCIMB 10007-Reference-Cited by-同舟云学术

Some Baeyer–Villiger oxidations using a monooxygenase enzyme from Pseudomonas putida NCIMB 10007

Published:1993 Issue:8 Volume: Page:699-701
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Grogan Gideon,Roberts Stanley M.,Willetts Andrew J.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930000699

Reference11 articles.

1. H. G. Davies , R. H.Green, D. R.Kelly and S. M.Roberts, Biotransformations in Preparative Organic Chemistry: the Use of Isolated Enzymes and Whole Cell Systems in Synthesis; Academic Press, 1989.

2. Microbiological Transformations 15. The Enantioselective Microbiological Baeyer-Villiger Oxidation of Alpha-Substituted Cyclopentanones

3. Microbiological transformations. 13. Direct synthesis of both S and R enantiomers of 5-hexadecanolide via an enantioselective microbiological Baeyer-Villiger reaction

4. Preparation of optically active 6′-fluorocarbocyclic nucleosides utilising an enantiospecific enzyme-catalysed Baeyer–Villiger type oxidation

5. Synthesis of compounds active against HIV: preparation of 6′-fluorocarbocyclic AZT (AZT = 3′-deoxy-3′-azidothymidine)

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