Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives-Reference-Cited by-同舟云学术

Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives

Published:2018 Issue:13 Volume:5 Page:2126-2131
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhang Xiying¹²³⁴⁵^ORCID,Liu Xiaohua¹²³⁴⁵^ORCID,Zhang Jianlin¹²³⁴⁵^ORCID,Zhang Dong¹²³⁴⁵^ORCID,Lin Lili¹²³⁴⁵^ORCID,Feng Xiaoming¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Green Chemistry & Technology

2. Ministry of Education

3. College of Chemistry

4. Sichuan University

5. Chengdu 610064

Abstract

A highly efficient catalytic asymmetric [3 + 2] cycloaddition/rearrangement cascade of thiazolium N-ylides with various electron-deficient 2-π components was achieved, providing a convenient method to access hydropyrrolo-thiazole and hydropyrrolo-thiazine derivatives.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C8QO00370J

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