Asymmetric bioreduction of keto groups of 4- and 5-Oxodecanoic acids/esters with a new carbonyl reductase-Reference-Cited by-同舟云学术

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Asymmetric bioreduction of keto groups of 4- and 5-Oxodecanoic acids/esters with a new carbonyl reductase

Published:2017-12 Issue: Volume:102 Page:35-39
ISSN:1566-7367
Container-title:Catalysis Communications
language:en
Short-container-title:Catalysis Communications

Author:

Zhang Chao^ORCID,Pan Jiang,Li Chun-Xiu,Bai Yun-Peng,Xu Jian-He

Funder

National Key Research and Development of China

National Natural Science Foundation of China

Shanghai Pujiang Program

Fundamental Research Funds for the Central Universities

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,General Chemistry,Catalysis

Reference35 articles.

1. Enantioselective Route to Ketones and Lactones from Exocyclic Allylic Alcohols via Metal and Enzyme Catalysis

2. Proline Catalyzed α-Aminoxylation Reaction in the Synthesis of Biologically Active Compounds

3. Recent progress in the chemistry and chemical biology of microbial signaling molecules: quorum-sensing pheromones and microbial hormones

4. Biocatalytic Methods for the Synthesis of Enantioenriched Odor Active Compounds

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1. Toward an environmentally friendly synthesis of chiral γ-lactones: A biocatalytically oxidative desymmetrization pathway;Molecular Catalysis;2024-10

2. Continuous-flow enzymatic synthesis of chiral lactones in a three-dimensional microfluidic reactor;Chinese Chemical Letters;2024-03

3. Mining and tailor-made engineering of a novel keto reductase for asymmetric synthesis of structurally hindered γ- and δ-lactones;International Journal of Biological Macromolecules;2024-03

4. Enantioselective synthesis of structurally diverse aryl γ-/δ- lactones using an engineered carbonyl reductase;Biochemical Engineering Journal;2023-11

5. The Synthesis of Chiral γ‐Lactones by Merging Decatungstate Photocatalysis with Biocatalysis;ChemCatChem;2022-08-22

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