Phosphine-catalyzed [5+1] annulation of δ-sulfonamido-substituted enones withN-sulfonylimines: a facile synthesis of tetrahydropyridines-Reference-Cited by-同舟云学术

Phosphine-catalyzed [5+1] annulation of δ-sulfonamido-substituted enones withN-sulfonylimines: a facile synthesis of tetrahydropyridines

Published:2018 Issue:7 Volume:9 Page:1831-1835
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Zhou Leijie¹²³⁴,Yuan Chunhao¹²³⁴,Zeng Yuan¹²³⁴,Liu Honglei¹²³⁴,Wang Chang¹²³⁴,Gao Xing¹²³⁴,Wang Qijun¹²³⁴,Zhang Cheng¹²³⁴^ORCID,Guo Hongchao¹²³⁴^ORCID

Affiliation:

1. Department of Applied Chemistry

2. China Agricultural University

3. Beijing 100193

4. China

Abstract

The first phosphine-catalyzed [5+1] annulation of enones withN-sulfonylimines works efficiently to give tetrahydropyridines.

Funder

NSFC

Guizhou University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/SC/C7SC04515H

Reference69 articles.

1. Enantioselective Phosphine Organocatalysis

2. Development of asymmetric phosphine-promoted annulations of allenes with electron-deficient olefins and imines

3. Advances in nucleophilic phosphine catalysis of alkenes, allenes, alkynes, and MBHADs

4. Recent Advances in Organocatalytic Asymmetric Morita–Baylis–Hillman/aza-Morita–Baylis–Hillman Reactions

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