Synthesis of thiazolidin-4-ones from α-enolic dithioesters and α-halohydroxamates-Reference-Cited by-同舟云学术

Synthesis of thiazolidin-4-ones from α-enolic dithioesters and α-halohydroxamates

Published:2021 Issue:32 Volume:45 Page:14508-14512
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Sun Jianguo¹²³⁴⁵,Wang Taimin⁶⁷⁴⁵,Zhu Xuecheng⁶⁷⁴⁵,Xu Wei⁶⁷⁴⁵^ORCID,Cheng Bin⁶⁷⁴⁵⁸,Zhai Hongbin¹²³⁴⁵

Affiliation:

1. State Key Laboratory of Chemical Oncogenomics

2. Shenzhen Engineering Laboratory of Nano Drug Slow-Release

3. Peking University Shenzhen Graduate School

4. Shenzhen 518055

5. China

6. Institute of Marine Biomedicine

7. Shenzhen Polytechnic

8. State Key Laboratory of Applied Organic Chemistry

Abstract

A facile access to thiazolidin-4-ones from α-enolic dithioesters and α-halohydroxamates in situ derived active 1,3-dipolar aza-oxyallyl cations was achieved under mild conditions.

Funder

National Natural Science Foundation of China

Shenzhen Science and Technology Innovation Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/NJ/D1NJ01970H

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