Improvement of enantioselective syntheses and chiral high resolution gas chromatographic analyses of (+)-2-allyl-2-carboethoxy-cyclopentanol.

Abstract:

:The improvement of the biocatalytic reduction of 2-allyl-carboethoxy-cyclopentanone (2) to the corresponding cyclopentanol derivative (+)-(1R,2R)-(1) was accomplished employing baker's yeast in organic media. This chiral cyclopentanol derivative (1), analyzed by high resolution gas chromatography performed over beta-cyclodextrin stationary phase, was obtained in 38% yield (> 99% e.e.).

journal_name

Chirality

journal_title

Chirality

authors

Fraga CA,Barreiro EJ,da Silva EF,dos Santos AR,KV Ramos MdaC,de Aquino Neto FR

doi

10.1002/(SICI)1520-636X(1997)9:4<321::AID-CHIR1>3.

subject

Has Abstract

pub_date

1997-01-01 00:00:00

pages

321-4

issue

4

eissn

0899-0042

issn

1520-636X

pii

10.1002/(SICI)1520-636X(1997)9:4<321::AID-CHIR1>3.

journal_volume

9

pub_type

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