Oxidant- and metal-free synthesis of 4(3H)-quinazolinones from 2-amino-N-methoxybenzamides and aldehydes via acid-promoted cyclocondensation and elimination
Author:
Affiliation:
1. Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency
2. School of Pharmaceutical Science and Technology
3. Tianjin University
4. Tianjin 300072, China
5. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)
Abstract
This paper presents a novel one-pot synthesis of biologically relevant 4(3H)-quinazolinones, in the absence of oxidants or heavy-metal catalysts.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA04331F
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1. Novel Nonpeptide CCK-B Antagonists: Design and Development of Quinazolinone Derivatives as Potent, Selective, and Orally Active CCK-B Antagonists
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