Semirational Engineering of a Thermostable Carbonyl Reductase for the Precision Synthesis of (2<i>R</i>,3<i>R</i>)-2-Methyl-2-benzyl-3-hydroxycyclopentanone and Its Analogues-Reference-Cited by-同舟云学术

Semirational Engineering of a Thermostable Carbonyl Reductase for the Precision Synthesis of (2R,3R)-2-Methyl-2-benzyl-3-hydroxycyclopentanone and Its Analogues

Published:2023-08-01 Issue:16 Volume:88 Page:11905-11912
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhu Liangyan¹²,Chen Xi¹²^ORCID,Feng Jinhui¹²^ORCID,Cui Yunfeng¹,Wu Qiaqing¹²^ORCID,Zhu Dunming¹²^ORCID

Affiliation:

1. National Center of Technology Innovation for Synthetic Biology, National Engineering Research Center of Industrial Enzymes and Tianjin Engineering Research Center of Biocatalytic Technology, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c01192

Reference23 articles.

1. Stereospecific Synthesis of (+)- and (−)-Cyclooctenone Derivatives Using a Ring Expansion Reaction with Me3SiSnBu3 and CsF

2. General synthetic approach to bicyclo[9.3.0]tetradecenone: a versatile intermediate to clavulactone and clavirolides

3. Enantioselective total synthesis of (+)-digitoxigenin

4. Efforts toward rapid construction of the cortistatin A carbocyclic core via enyne-ene metathesis

5. Determining a Synthetic Approach to Pierisformaside C

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