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ChemInform Abstract: Selective Synthesis of 1-, and 3-Carbomethoxy 2-Tetralol Stereoisomers by Microbial Reduction of the Corresponding Tetralones.

✍ Scribed by C. ABALAIN; D. BUISSON; R. AZERAD

Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
28
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable via the β€œReferences” option.

πŸ“œ SIMILAR VOLUMES

Selective synthesis of 1-, and 3-carbome
Selective synthesis of 1-, and 3-carbomethoxy 2-tetralol stereoisomers by microbial reduction of the corresponding tetralones
✍ CΓ©cile Abalain; Didier Buisson; Robert Azerad πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 English βš– 803 KB

The microbial reduction of ~-ketoesters derived from 2-tetralone has been shown to produce good yields of 2-hydroxy-l-carboxy-or 3-hydroxy-2-carboxyesters. Baker's yeast invariably affords a high enantiomeric purity cis-hydroxyester, while fungi strains may produce, sometimes exclusively, cisor tran

ChemInform Abstract: A Concise Synthesis
ChemInform Abstract: A Concise Synthesis of 1-Substituted-2-tetralones by Selective Diol Dehydration Leading to Ketone Transposition.
✍ Bruce L. Jensen; Sergei V. Slobodzian πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 33 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v