Electro-induced O–S bonding reaction targeting biological macromolecules-Reference-Cited by-全球学者库

Electro-induced O–S bonding reaction targeting biological macromolecules

Published:2024 Issue: Volume: Page:
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Jiang Shuqiang¹,Xiao Longyu¹,Pan Li²,Huang Qiaoyu³,Huo Fujin¹,Gao Meng¹^ORCID,Lu Cuifen¹^ORCID,Wu Pan²,Weng Yue¹^ORCID

Affiliation:

1. Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecule, State Key Laboratory of Biocatalysis and Enzyme Engineering, School of Chemistry and Chemical Engineering, Hubei University, Wuhan, P. R. China

2. State Key Laboratory of Biocatalysis and Enzyme Engineering, School of Life Sciences, Hubei University, Wuhan, 430062, P. R. China

3. Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei Key Laboratory of Polymer Materials, School of Materials Science and Engineering, Hubei University, Wuhan, 430062, P. R. China

Abstract

This study endeavors to explore the utilization of aromatic sulfinates as bioconjugation handles, addressing the challenges associated with the modification of Tyrosine and paving the way for innovative approaches to biomolecule functionalization.

Funder

Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Ministry of Education

National Natural Science Foundation of China

State Key Laboratory of Biocatalysis and Enzyme Engineering

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01794J

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