Visible-Light-Driven α-C(sp3)–H Bond Functionalization of Glycine Derivatives

Author:

Tian Yao1,Bu Xiubin1,Chen Yuanrui1,Wang Luohe1,E Junnan1,Zeng Jing1,Xu Hao23,Han Aihong1,Yang Xiaobo12ORCID,Zhao Zhen1

Affiliation:

1. Institute of Catalysis for Energy and Environment, College of Chemistry and Chemical Engineering, Shenyang Normal University, Shenyang 110034, China

2. Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, China

3. Institute of Functional Organic Molecular Engineering, College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, China

Abstract

The glycine motif is widely prevalent in bioactive peptides. Thus, the direct and precise modification of glycine derivatives has attracted significant attention over the past few decades. Among various protocols for the modification of glycine derivatives, the visible-light-driven direct α-C(sp3)–H bond functionalization of glycine derivatives has emerged as a powerful tool to achieve this objective, owing to its merits in atom economy, selectivity, reaction simplicity, and sustainability. This review summarizes the recent advancements in visible-light-driven direct α-C(sp3)–H bond functionalization of glycine derivatives. The contents of this review are organized based on the photocatalysts employed and the various reaction modes in the functionalization process. The mechanism, the challenges encountered, and future trends are also discussed, enabling readers to understand the current developmental status in this field.

Funder

Basic Scientific Project of the Universities in Liaoning Province

Liaoning Revitalization Talents Program

Natural Science Foundation of Shenyang

Youth Cross-disciplinary Fund of Henan University

Engineering Technology Research Centre of Catalysis for Energy and Environment-Major Platform for Science and Technology of the Universities in Liaoning Province

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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