Transition-Metal-Free Disulfuration of Amides with Trisulfide Dioxides via Formation of Unaccessible S–S

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Transition-Metal-Free Disulfuration of Amides with Trisulfide Dioxides via Formation of Unaccessible S–S–N Bonds

Published:2024-02-16 Issue:5 Volume:89 Page:3590-3596
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yu Yue¹²^ORCID,Chen Jianxin¹,Huang Mingzhou¹,Jiang Yuhao¹,Zhou Xianhang¹,Wang Jinsong¹,Li Jiaxin¹,Cao Hua¹²^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Guangdong Provincial Key Laboratory of Advanced Drug Delivery, Guangdong Provincial Engineering Center of Topical Precise Drug Delivery System, Guangdong Pharmaceutical University, Guangzhou, 510006, P. R. China

2. Guangdong Pharmaceutical University-University of Hong Kong Joint Biomedical Innovation Platform, Zhongshan, 528437, P. R. China

Funder

Zhongshan Science and Technology Bureau

Guangdong Provincial Department of Science and Technology

Guangzhou Municipal Science and Technology Project

Zhongshan City

Special Funds of Key Disciplines Construction from Guangdong and Zhongshan Cooperating

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02497

Reference37 articles.

1. Mapping native disulfide bonds at a proteome scale

2. Multifaceted Roles of Disulfide Bonds. Peptides as Therapeutics

3. Antioxidant Defense by Thioredoxin Can Occur Independently of Canonical Thiol-Disulfide Oxidoreductase Enzymatic Activity

4. Construction of sulfur-containing moieties in the total synthesis of natural products

5. Alleviating Cellular Oxidative Stress through Treatment with Superoxide‐Triggered Persulfide Prodrugs

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