An efficient metal-free desulfurization strategy promoted by Togni-II reagent-Reference-Cited by-同舟云学术

An efficient metal-free desulfurization strategy promoted by Togni-II reagent

Published:2023 Issue:43 Volume:59 Page:6513-6516
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Jun¹,Liu Haiyun¹,Teng Shuang²,Liao Zhiwen²,Meng Lingkui²,Wan Qian²^ORCID,Dong Suwei¹^ORCID

Affiliation:

1. State Key Laboratory of Natural and Biomimetic Drugs, Chemical Biology Center, and Department of Chemical Biology at School of Pharmaceutical Sciences, Peking University, Beijing 100191, China

2. Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Huazhong University of Science and Technology, 13 Hangkong Road, Wuhan, Hubei 430030, China

Abstract

Desulfurization is a versatile synthetic tool in organic synthesis, particularly in peptide chemistry, where it offers an effective conversion strategy for compounds that contain mercaptan groups.

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC00983A

Reference25 articles.

1. The Action of Raney Nickel on Organic Sulfur Compounds.

2. Desulfurization of Thioketals into Methylene and Methyl Derivatives: Nickel or not Nickel?

3. Recent advances and applications of reductive desulfurization in organic synthesis

4. Intermolecular Phosphite-Mediated Radical Desulfurative Alkene Alkylation Using Thiols

5. Reductive C–C Coupling by Desulfurizing Gold-Catalyzed Photoreactions

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