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2000
Volume 5, Issue 2
  • ISSN: 2213-3461
  • E-ISSN: 2213-347X

Abstract

Oxidation of 2-(substituted thio) quinazolines in THF and aqueous media using stoichiometric amounts of oxone afforded their corresponding 2-(substituted sulfonyl)quinazolines with excellent selectivity (75-94% yield). This versatile synthetic protocol proved efficient with various substituted thio quinazoline compounds as substrates. All the twelve products were characterized by melting range, infrared, 1H-NMR, 13C-NMR and mass spectrometry.

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/content/journals/cgc/10.2174/2213346105666180605123417
2018-08-01
2025-09-04
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/content/journals/cgc/10.2174/2213346105666180605123417
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  • Article Type:
    Research Article
Keyword(s): chemo-selective; m-CPBA; optimization; Oxone; sulfones; thioquinazolines
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