Asymmetric Synthesis of Both Antipodes of β-Hydroxy Nitriles and β-Hydroxy Carboxylic Acids via Enzymatic Reduction or Sequential Reduction/Hydrolysis-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Both Antipodes of β-Hydroxy Nitriles and β-Hydroxy Carboxylic Acids via Enzymatic Reduction or Sequential Reduction/Hydrolysis

Published:2009-01-22 Issue:4 Volume:74 Page:1658-1662
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ankati Haribabu¹,Zhu Dunming¹,Yang Yan¹,Biehl Edward R.¹,Hua Ling¹

Affiliation:

1. Department of Chemistry, Southern Methodist University, Dallas, Texas 75275, State Engineering Laboratory for Industrial Enzymes, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China, and China Research Center, Genencor, A Danisco Division, Shanghai 200335, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo802495f

Reference64 articles.

1. Synthesis of β-Hydroxypropanoic Acid Derivatives as Potential Anti-inflammatory, Analgesic and Antimicrobial Agents

2. .alpha.,.alpha.-Difluoro-.beta.-aminodeoxystatine-containing renin-inhibitory peptides

3. A stereospecific synthesis of 3-aminodeoxystatine

4. A protocol for the efficient synthesis of enantiopure .beta.-substituted .beta.-lactones

5. A Facile Synthesis of Optically Pure (?)-(S)-Ipsenol Using a Chiral Titanium Complex

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