Preparation of optically active 6′-fluorocarbocyclic nucleosides utilising an enantiospecific enzyme-catalysed Baeyer–Villiger type oxidation
Authors:
- Melissa S. LevittMLMelissa S. Levitt
- Roger F. NewtonRNRoger F. Newton
- Stanley M. RobertsSRStanley M. Roberts
- Andrew J. WillettsAWAndrew J. Willetts
- 1 January 1990
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 8,p. 619-620
Abstract
Kinetic resolution of the racemic ketone (±)-(1) was achieved using Acinetobacter NCIB 9871: the optically active norbornanone was converted into the carbocyclic nucleosides (5) and (7).Keywords
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