Customizing the Enantioselectivity of a Cyclohexanone Monooxygenase by a Strategy Combining “Size‐Probes” with in silico Study-Reference-Cited by-同舟云学术

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Customizing the Enantioselectivity of a Cyclohexanone Monooxygenase by a Strategy Combining “Size‐Probes” with in silico Study

Published:2019-09-30 Issue:20 Volume:11 Page:5085-5092
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Hu Yujing¹,Xu Jian¹,Cen Yixin¹,Li Danyang¹,Zhang Yu¹,Huang Meilan²,Lin Xianfu¹,Wu Qi¹^ORCID

Affiliation:

1. Department of ChemistryZhejiang University Hangzhou 310027 China

2. School of Chemistry and Chemical EngineeringQueen's University Belfast BT9 5AG UK

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.201901200

Reference61 articles.

1.

2. Asymmetric Baeyer−Villiger Oxidations of 4-Mono- and 4,4-Disubstituted Cyclohexanones by Whole Cells of Engineered Escherichia coli

3. The enzymatic Baeyer-Villiger oxidation: enantioselective synthesis of lactones from mesomeric cyclohexanones

4. Access to Optically Pure 4- and 5-Substituted Lactones: A Case of Chemical−Biocatalytical Cooperation

5. The enzymatic baeyer-villiger oxidation: A study of 4-substituted cyclohexanones

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