Nickel-catalyzed selective disulfide formation by reductive cross-coupling of thiosulfonates-Reference-Cited by-同舟云学术

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Nickel-catalyzed selective disulfide formation by reductive cross-coupling of thiosulfonates

Published:2024 Issue: Volume: Page:
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Yuan Tingting¹²^ORCID,Chen Xiang-Yu²³^ORCID,Ji Tengfei²,Yue Huifeng¹^ORCID,Murugesan Kathiravan¹,Rueping Magnus¹^ORCID

Affiliation:

1. KAUST Catalysis Center, KCC, King Abdullah University of Science and Technology, KAUST, Thuwal 23955-6900, Saudi Arabia

2. Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany

3. School of Chemical Science, University of Chinese Academy of Science, Beijing 10049, China

Abstract

A mild and straightforward synthetic route has been established for the preparation of disulfide, enabling the selective and efficient synthesis of both symmetric and unsymmetrical disulfide compounds.

Funder

King Abdullah University of Science and Technology

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC02969K

Reference83 articles.

1. Lipoic Acid: Its Antioxidant and Anti-Inflammatory Role and Clinical Applications

2. Disulfide- and Multisulfide-Containing Metabolites from Marine Organisms

3. Dithiolopyrrolones: biosynthesis, synthesis, and activity of a unique class of disulfide-containing antibiotics

4. PEGylation of native disulfide bonds in proteins

5. An Overview of Recent Advances in the Synthesis of Organic Unsymmetrical Disulfides

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