Diversity‐Oriented Synthesis of 2‐Iminothiazolidines: Pushing the Boundaries of the Domino Nucleophilic Displacement/Intramolecular <i>anti</i> ‐Michael Addition Process-Reference-Cited by-同舟云学术

Diversity‐Oriented Synthesis of 2‐Iminothiazolidines: Pushing the Boundaries of the Domino Nucleophilic Displacement/Intramolecular anti ‐Michael Addition Process

Published:2022-04-20 Issue:15 Volume:2022 Page:
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:European J Organic Chem

Author:

Ferreira Misael¹,Munaretto Laiéli S.¹,Gouvêa Daniela P.¹,Bortoluzzi Adailton J.¹,Sá Marcus M.¹

Affiliation:

1. Departamento de Química Universidade Federal de Santa Catarina Florianópolis SC 88040-900 Brazil

Funder

Fundação de Amparo à Pesquisa e Inovação do Estado de Santa Catarina

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202101562

Reference81 articles.

1. Synthetic Routes to 2-Iminothiazolidines: State-of-the-Art 2006-2020

3. Design, Synthesis and Biological Evaluation of 2‐(naphthoyl) iminothiazolidin‐4‐ones as Potential Anticancer Agents

4. Synthesis, biological evaluation and computational studies of novel iminothiazolidinone benzenesulfonamides as potent carbonic anhydrase II and IX inhibitors

5. Synthetic approaches towards 2-iminothiazolidines: an overview

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