Enantioselectivity and Reactivity Enhancement by 1,1,3,3-Tetramethylguanidine in Bisguanidinium-Catalyzed Asymmetric Alkylation for Construction of Indole Alkaloid Marine Natural Products-Reference-Cited by-同舟云学术

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Enantioselectivity and Reactivity Enhancement by 1,1,3,3-Tetramethylguanidine in Bisguanidinium-Catalyzed Asymmetric Alkylation for Construction of Indole Alkaloid Marine Natural Products

Published:2023-11-21 Issue:24 Volume:13 Page:15708-15714
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Zuo Xiong¹,Wan Zhenghao¹,Liao Zhihuan¹,Wang Chao²^ORCID,Tan Choon-Hong³^ORCID,Huo Shuaidong¹^ORCID,Zong Lili¹^ORCID

Affiliation:

1. Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China

2. Institute of Advanced Synthesis, School of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, China

3. School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore 637371, Singapore

Funder

National Natural Science Foundation of China

Xiamen University

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.3c03812

Reference66 articles.

1. PROTEIN PRENYLATION: Molecular Mechanisms and Functional Consequences

2. Getting a handle on protein prenylation

3. Protein prenylation restrains innate immunity by inhibiting Rac1 effector interactions

4. Dual chemical probes enable quantitative system-wide analysis of protein prenylation and prenylation dynamics

5. Protein Prenylation, et cetera--Signal Transduction in Two Dimensions

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