Enantioselective sulfonylation using sodium hydrogen sulfite, 4-substituted Hantzsch esters and 1-(arylethynyl)naphthalen-2-ols-Reference-Cited by-同舟云学术

Enantioselective sulfonylation using sodium hydrogen sulfite, 4-substituted Hantzsch esters and 1-(arylethynyl)naphthalen-2-ols

Published:2023 Issue:1 Volume:10 Page:92-98
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Xinhua¹,Ding Qiuping¹^ORCID,Yang Chenxi²,Yang Jianguo²,Wu Jie²³⁴^ORCID

Affiliation:

1. College of Chemistry & Chemical Engineering, Jiangxi Normal University, Nanchang, 330022, China

2. School of Pharmaceutical and Chemical Engineering & Institute for Advanced Studies, Taizhou University, 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

4. School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China

Abstract

Synthesis of sulfonyl-containing axially chiral styrenes through a catalytic asymmetric reaction of 4-substituted Hantzsch esters, sodium hydrogen sulfite and 1-(arylethynyl)naphthalen-2-ols is reported.

Funder

Henan Normal University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D2QO01654K

Reference77 articles.

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2. Insertion of sulfur dioxide via a radical process: an efficient route to sulfonyl compounds