Synthesis of Spirocyclohexanone Ring Containing Thiazolidine Nucleus: A Regioselective Approach-Reference-Cited by-同舟云学术

Synthesis of Spirocyclohexanone Ring Containing Thiazolidine Nucleus: A Regioselective Approach

Published:2005-06 Issue:6 Volume:2005 Page:345-347
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Chande Madhukar S.¹,Suryanarayan Vijay¹²

Affiliation:

1. Department of Chemistry, Organic Chemistry Division, The Institute of Science, Mumbai 400 032, India

2. Present address: Department of Chemistry, University of Wisconsin, Madison, USA

Abstract

The paper highlights the Michael addition reactions of 2-arylimino-3-aryl-thiazolidin-4-one 1 with acceptors like methyl acrylate and acrylonitrile to furnish the diadducts 5 and 8. Dieckmann condensation of 5 affords the spirocyclohexanone derivative. Also discussed is the interaction of 1 with 1,5-diarylpenta-1,4-dien-3-ones 9.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/0308234054506749

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4. Studies on 4-Hydroxycoumarins. V. The Condensation of α,β-Unsaturated Ketones with 4-Hydroxycoumarin1

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