| Literature DB >> 21589958 |
Riccardo Mossetti1, Tracey Pirali, Dèsirèe Saggiorato, Gian Cesare Tron.
Abstract
Up to now, the synthesis of quinazolinones has required lengthy synthetic procedures. Here, we describe an innovative one-pot multicomponent reaction leading to highly substituted quinazolinones. We believe that this novel transformation may open the door for the generation of new and pharmacologically active quinazolinones, but, most important of all, the resurrection of the imide-Ugi scaffold paves the way for the synthesis of novel molecular architectures. This journal is © The Royal Society of Chemistry 2011Entities:
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Year: 2011 PMID: 21589958 DOI: 10.1039/c1cc12067k
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222