C(sp<sup>3</sup>)–H fluorosulfonylvinylation/aza-Michael addition approach to FSO<sub>2</sub>-functionalized tetrahydropyridines-Reference-Cited by-同舟云学术

C(sp³)–H fluorosulfonylvinylation/aza-Michael addition approach to FSO₂-functionalized tetrahydropyridines

Published:2023 Issue:15 Volume:10 Page:3805-3810
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Shi Shuai¹,Zhao Xueyan¹,Chen Dengfeng¹,Luo Jinyue¹,Liao Saihu²,Huang Shenlin¹^ORCID

Affiliation:

1. Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, International Innovation Center for Forest Chemicals and Materials, Nanjing Forestry University, Nanjing 210037, China

2. State Key Laboratory of Physical Chemistry of Solid Surfaces, Xiamen University, Xiamen 361005, China

Abstract

We have developed an efficient approach for the synthesis of FSO2-functionalized tetrahydropyridines from propargyl alcohols, FSO2Cl, and anilines.

Funder

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/D3QO00639E

Reference55 articles.

1. Sulfur(VI) Fluoride Exchange (SuFEx): Another Good Reaction for Click Chemistry

2. Sulfonyl Fluorides (SFs): More Than Click Reagents?

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