One-pot synthesis of nitrocyclopropane: α-Amylase-catalyzed Michael addition initiated ring-closure sequence reactions-Reference-Cited by-同舟云学术

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One-pot synthesis of nitrocyclopropane: α-Amylase-catalyzed Michael addition initiated ring-closure sequence reactions

Published:2016-12 Issue: Volume:134 Page:1-8
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

Zhang Xue-Dong,Song Jian,Gao Na,Guan Zhi,He Yan-Hong

Funder

National Natural Science Foundation of China

2014 Chongqing Graduate Education Reform Project

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference45 articles.

1. Biocatalysis for pharmaceutical intermediates: the future is now

2. Artificial Metalloenzymes and Metallopeptide Catalysts for Organic Synthesis

3. Enzyme promiscuity: mechanism and applications

4. Asymmetric aldol reactions catalyzed by the promiscuous aldo–ketoreductase enzyme

5. Ficin-catalyzed asymmetric aldol reactions of heterocyclic ketones with aldehydes

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1. A decade update on the promiscuity of α-amylase in organic synthesis;Tetrahedron;2024-04

2. Enzyme-catalyzed addition of diazo compounds to in-situ generated imines;Tetrahedron;2023-05

3. Immobilization of trypsin onto polyamidoamine dendrimer functionalized iron oxide nanoparticles and its catalytic behavior towards spirooxindole-pyran derivatives in aqueous media;Materials Today Communications;2021-03

4. Recent Trends in the Development of Novel Catalysts for Asymmetric Michael Reaction;Current Organic Chemistry;2020-10-01

5. Biocatalytic Aza‐Michael Addition of Aromatic Amines to Enone Using α‐Amylase in Water;Advanced Synthesis & Catalysis;2019-12-23

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