Catalyst-free synthesis of thiazolidines via sequential hydrolysis/rearrangement reactions of 5-arylidenethiazolidin-4-ones at room temperature
Author:
Affiliation:
1. Shanghai Key Laboratory of Chemical Biology
2. School of Pharmacy
3. East China University of Science and Technology
4. Shanghai 200237
5. China
Abstract
Functionalized thiazolidines were obtained via the rearrangement reactions of 5-arylidenethiazolidin-4-ones at room temperature.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/OB/C7OB02924A
Reference49 articles.
1. Bicyclic thiazolidine lactam peptidomimetics of the dopamine receptor modulating peptide Pro-Leu-Gly-NH2
2. Synthesis and preliminary evaluation of some pyrazine containing thiazolines and thiazolidinones as antimicrobial agents
3. Peroxidase catalyzed formation of azine pigments—a convenient and sensitive method for the identification of human cells with positive myeloperoxidase reactivity
4. A Novel Entry toward 2-Imino-1,3-thiazolidines and 2-Imino-1,3-thiazolines by Ring Transformation of 2-(Thiocyanomethyl)aziridines
5. Natural Product-Inspired Synthesis of Thiazolidine and Thiazolidinone Compounds and their Anticancer Activities
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