Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ϵ-Lactone, and Cyclitols from Biocatalytically Derived β-Hydroxy Esters as Chiral Precursors-Reference-Cited by-同舟云学术

Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ϵ-Lactone, and Cyclitols from Biocatalytically Derived β-Hydroxy Esters as Chiral Precursors

Published:2014-07-15 Issue:24 Volume:2014 Page:5229-5246
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Das Debabrata,Halder Joydev,Bhuniya Rajib,Nanda Samik

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201402521/fullpdf

Reference111 articles.

1. Stereochemical control of microbial reduction. 17. A method for controlling the enantioselectivity of reductions with bakers' yeast

2. Asymmetric Synthesis of β-Hydroxy Esters and α-Alkyl-β-hydroxy Esters by Recombinant Escherichia coli Expressing Enzymes from Baker's Yeast

3. A Two-Step, One-Pot Enzymatic Synthesis of 2-Substituted 1,3-Diols

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