Synthesis of 3a, 4-dihydro-8-substituted-3H-isoxazolo c-4,3] thiapyrano 5,6-3,2] quinolines

Prabhuswamy, B. and Ambekar, S. Y. (1999) Synthesis of 3a, 4-dihydro-8-substituted-3H-isoxazolo c-4,3] thiapyrano 5,6-3,2] quinolines. Synthetic Communications, 29 (20). pp. 3477-3485. ISSN 0039-7911

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Official URL: https://doi.org/10.1080/00397919908085980

Abstract

Condensation of 2-chloro-3-formylquinoline 1a-c with allylthiol 2 afforded 2-allysulfanyl-3-formylquinolines 3a-c, Oximation followed by oxidation of 3a-c with NaOCl or chloramine-T, in cold or mercuric acetate resulted in the formation of respective nitrile oxides, which underwent insitu intramolecular 1,3-dipolar cycloaddition reaction and afforded the title compounds 5a-c in high yield.

Item Type: Article
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: Vasantha
Date Deposited: 22 Jan 2020 10:38
Last Modified: 22 Jan 2020 10:38
URI: http://eprints.uni-mysore.ac.in/id/eprint/11180

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