QUEST Leibniz Research School

Remarkable kinetic resolution of chiral β-keto esters by baker's yeast reduction

authored by: Marcus Eh, Markus Kalesse
Abstract: The reduction of chiral β-keto esters with baker's yeast is described. Reduction of 10 yields highly functionalized diol 11 with excellent stereoselectivity and generates a useful intermediate for natural product syntheses.
Organisation(s): Institute of Organic Chemistry
Type: Article
Journal: SYNLETT
Volume: 1995
Pages: 837-838
No. of pages: 2
ISSN: 0936-5214
Publication date: 08.1995
Publication status: Published
Peer reviewed: Yes
ASJC Scopus subject areas: Organic Chemistry
Electronic version(s): https://doi.org/10.1055/s-1995-5083 (Access: Unknown)

BibTeX

@article{c325ecdb1d3c4010949d9bbfe14b7b42,
title = "Remarkable kinetic resolution of chiral β-keto esters by baker's yeast reduction",
abstract = "The reduction of chiral β-keto esters with baker's yeast is described. Reduction of 10 yields highly functionalized diol 11 with excellent stereoselectivity and generates a useful intermediate for natural product syntheses.",
keywords = "1,3-diols, Baker's yeast reduction, kinetic resolution, β-keto esters",
author = "Marcus Eh and Markus Kalesse",
note = "Publisher Copyright: {\textcopyright} 1995 Georg Thieme Verlag, Rudigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.",
year = "1995",
month = aug,
doi = "10.1055/s-1995-5083",
language = "English",
volume = "1995",
pages = "837--838",
journal = "SYNLETT",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "8",
}

Last Change: 09.02.23; Dr. A. Wanner Print