崔

崔成森 (Chengsen Cui)

chinese academy of sciences邮箱:cuichs@tib.cas.cn

H指数:13

被引数:616

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An Engineered Enzyme Catalyzing Tandem Reductive Aminations for Synthesizing Tertiary Amines

Angewandte Chemie-International Edition

IF16.9

2026-07-270

PRE

Substrate-Guided Engineering of Imine Reductases: A Strategy for Synthesizing Tertiary Amine N-Heterocycles

底物引导的亚胺还原酶工程：一种合成叔胺N-杂环的策略

Chemistry - A European Journal

IF3.7

2026-05-180

PRE

Synergistic CRISPR–Cas9 Host Engineering and Enzyme Evolution for Enantioselective Synthesis of a Vibegron Pyrrolidine Intermediate

协同CRISPR–Cas9宿主工程与酶进化在振动罗环丙烷中间体制备中的对映选择性合成

Organic Letters

IF5

2026-03-160

PRE

Chemoenzymatic Synthesis of Unnatural Ergot Alkaloid; Demethyl Chanoclavine

化学酶法合成非天然麦角生物碱；去甲基查诺克林

ACS Catalysis

IF13.1

2026-03-020

PRE

Enzymatic Amination for Stereocontrolled Functionalization of Cyclohexanones

酶促氨基化用于环己酮的手性控制功能化

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2025-05-080

PRE

Synthetic Nicotinamide Cofactors as Alternatives to NADPH in Imine Reductase-Catalyzed Reactions (vol 26, pg 7821, 2024)

ORGANIC LETTERS

IF5

2024-12-200

PRE

Substrate specificity of a branch of aromatic dioxygenases determined by three distinct motifs

芳香族双加氧酶的一个分支的底物特异性由三个不同的基序决定

NATURE COMMUNICATIONS

IF15.7

2024-09-031

PRE

Synthetic Nicotinamide Cofactors as Alternatives to NADPH in Imine Reductase-Catalyzed Reactions

ORGANIC LETTERS

IF5

2024-08-230

PRE

An unexpected role of EasDaf: catalyzing the conversion of chanoclavine aldehyde to chanoclavine acid

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY

IF4.3

2024-05-070

OAAI

Peroxygenase-Enabled Reductive Kinetic Resolution for the Enantioenrichment of Organoperoxides

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2024-04-030

PRE

Chemoenzymatic Synthesis of Selegiline: An Imine Reductase-Catalyzed Approach

MOLECULES

IF4.6

2024-03-162

OAAI

Vanadium-Containing Chloroperoxidase-Catalyzed Versatile Valorization of Phenols and Phenolic Acids

ACS CATALYSIS

IF13.1

2024-01-180

PRE

Total Synthesis of UCS1025A via Tandem Carbonylative Stille Cross Coupling and Diels-Alder Reaction

通过串联的羰基Stille交叉耦合和diels-alder反应全合成UCS1025A

CHINESE JOURNAL OF CHEMISTRY

IF5.5

2023-08-174

Structure-guided semi-rational design of an imine reductase for enantio-complementary synthesis of pyrrolidinamine

CHEMICAL SCIENCE

IF7.4

2023-01-0112

OAAI

Rational enzyme design for enabling biocatalytic Baldwin cyclization and asymmetric synthesis of chiral heterocycles

NATURE COMMUNICATIONS

IF15.7

2022-12-1915

OAAI

Actinomycetes-derived imine reductases with a preference towards bulky amine substrates

COMMUNICATIONS CHEMISTRY

IF6.2

2022-10-0813

OAAI

Chemoenzymatic Hunsdiecker-Type Decarboxylative Bromination of Cinnamic Acids

ACS CATALYSIS

IF13.1

2022-04-0413

OAAI

Flow Chemistry-Enabled Divergent and Enantioselective Total Syntheses of Massarinolin A, Purpurolides B, D, E, 2,3-Deoxypurpurolide C, and Structural Revision of Massarinolin A

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2021-09-1515

OAAI

Total Synthesis and Target Identification of the Curcusone Diterpenes

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

IF15.6

2021-03-1123

Dual-purpose isocyanides produced by Aspergillus fumigatus contribute to cellular copper sufficiency and exhibit antimicrobial activity

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2021-02-1539

崔成森 (Chengsen Cui)

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