A reductive Sandmeyer-type reaction for the synthesis of sulfoxides from anilines under photocatalysis-Reference-Cited by-同舟云学术

A reductive Sandmeyer-type reaction for the synthesis of sulfoxides from anilines under photocatalysis

Published:2023 Issue:12 Volume:10 Page:3033-3038
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Peng Gangqi¹,Cheng Hao¹,Cheng Xiya¹,He Yang¹,An Yuanyuan¹^ORCID,Wu Jie²³^ORCID,Zheng Danqing¹^ORCID

Affiliation:

1. State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, South Puzhu Road 30, Nanjing 210009, China

2. School of Pharmaceutical and Chemical Engineering & Institute for Advanced Studies, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, China

3. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

Abstract

A reductive Sandmeyer-type sulfinylation reaction of aryldiazonium salts with sodium sulfinates is reported, affording a range of valuable sulfoxides in a radical substitution pathway.

Funder

Natural Science Foundation of Jiangsu Province

Nanjing Tech University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00297G

Reference62 articles.

1. Forazoline A: Marine-Derived Polyketide with Antifungal In Vivo Efficacy

2. S-Alkenyl Cysteine Sulfoxide and Its Antioxidant Properties from Allium cepa var. tropeana (Red Onion) Seeds