Trace water in a BF<sub>3</sub>·OEt<sub>2</sub> system: a facile access to sulfinyl alkenylsulfones from alkynes and sodium sulfinates-Reference-Cited by-同舟云学术

Trace water in a BF₃·OEt₂ system: a facile access to sulfinyl alkenylsulfones from alkynes and sodium sulfinates

Published:2023 Issue:38 Volume:21 Page:7776-7781
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yu Shi-Wei¹,Chen Zu-Jia¹,Chen Zhao-Hua¹,Chen Si-Hong¹,Yang Kai²,Xu Wen-Jin¹,Wang Zhao-Yang¹^ORCID

Affiliation:

1. School of Chemistry, South China Normal University; GDMPA Key Laboratory for Process Control and Quality Evaluation of Chiral Pharmaceuticals; Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine; Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, Guangzhou, Guangdong 510006, P. R. China

2. College of pharmacy, Gannan Medical University, Ganzhou 341000, P. R. China

Abstract

An efficient and operationally simple synthesis of β-sulfinyl alkenylsulfones through a BF3·OEt2-promoted reaction of alkynes and sodium sulfinates is developed.

Funder

Basic and Applied Basic Research Foundation of Guangdong Province

National Natural Science Foundation of China

Natural Science Foundation of Jiangxi Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB01249B

Reference44 articles.

1. Total Synthesis of (−)-Glionitrin A and B Enabled by an Asymmetric Oxidative Sulfenylation of Triketopiperazines

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