Transition metal free intramolecular S-arylation: One-pot synthesis of thiochromen-4-ones

Jenifer Vijay, T. A. and Nandeesh, K. N. and Raghavendra, G. M. and Rangappa, K. S. and Mantelingu, K. (2013) Transition metal free intramolecular S-arylation: One-pot synthesis of thiochromen-4-ones. Tetrahedron Letters, 54 (48). pp. 6533-6537. ISSN 0040-4039

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Official URL: http://doi.org/10.1016/j.tetlet.2013.09.094

Abstract

A convenient one-pot method for the synthesis of thiochromen-4-ones by the condensation of 2′-haloacetophenone and dithioesters at room temperature in the presence of NaH in DMF in moderate to good yields has been developed. The method involves unusual intramolecular S-arylation. The reaction is operationally facile, readily scalable and offers rapid entry into substituted chromene-4-ones.

Item Type: Article
Uncontrolled Keywords: article, unclassified drug, chemical structure, mass spectrometry, heterocyclic compound, chemical reaction, proton nuclear magnetic resonance, arylation, screening, one pot synthesis, carbon nuclear magnetic resonance, chromene derivative, natural product, thiochromen 4 one, thioflavonone
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: Arshiya Kousar Library Assistant
Date Deposited: 23 Sep 2019 06:21
Last Modified: 23 Sep 2019 06:21
URI: http://eprints.uni-mysore.ac.in/id/eprint/7945

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