Lawesson's reagent promoted deoxygenation of azlactones for the syntheses of 2,4-disubstituted thiazoles-Reference-Cited by-同舟云学术

Lawesson's reagent promoted deoxygenation of azlactones for the syntheses of 2,4-disubstituted thiazoles

Published:2022 Issue:48 Volume:20 Page:9589-9592
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yin Gaofeng¹,Wang Xiaodong¹,Wang Yuqing¹,Shi Tao¹^ORCID,Zeng Yaofu²^ORCID,Wang Yuying³,Peng Xue²^ORCID,Wang Zhen²^ORCID

Affiliation:

1. School of Pharmacy, Lanzhou University, West Donggang Road. No. 199, Lanzhou 730000, China

2. School of Pharmaceutical Science, Hengyang Medical School, University of South China, West Changsheng Road. No. 28, Hengyang 421001, China

3. State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China

Abstract

A new method for the straightforward syntheses of 2,4-disubstituted thiazoles from azlactones via deoxygenation with Lawesson's reagent has been developed.

Funder

Recruitment Program of Global Experts

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01939F

Reference65 articles.

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