DMAP-promoted domino annulation of β-ketothioamides with internal alkynes: a highly regioselective access to functionalized 1,3-thiazolidin-4-ones at room temperature-Reference-Cited by-同舟云学术

DMAP-promoted domino annulation of β-ketothioamides with internal alkynes: a highly regioselective access to functionalized 1,3-thiazolidin-4-ones at room temperature

Published:2014 Issue:23 Volume:4 Page:11640-11647
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Verma Girijesh Kumar¹²³⁴,Shukla Gaurav¹²³⁴,Nagaraju Anugula¹²³⁴,Srivastava Abhijeet¹²³⁴,Raghuvanshi Keshav⁵⁶⁷,Singh Maya Shankar¹²³⁴

Affiliation:

1. Department of Chemistry

2. Faculty of Science

3. Banaras Hindu University

4. Varanasi-221005, India

5. Institut fuer Organische und Biomolekulare Chemie

6. Georg-August-Universität Göttingen

7. 37077 Gottingen, Germany

Abstract

One-pot DMAP-mediated regioselective access to functionalized 1,3-thiazolidin-4-ones has been achieved via annulation of β-ketothioamides with internal alkynes.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA00131A

Reference56 articles.

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3. N-Heterocyclic Carbene Catalyzed Domino Reactions

4. Asymmetric organocascades involving the formation of two C–heteroatom bonds from two distinct heteroatoms

5. Stereocontrolled Domino Reactions

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