| Literature DB >> 28653839 |
Seuli Parua1, Siuli Das1, Rina Sikari1, Suman Sinha1, Nanda D Paul1.
Abstract
In this paper, we report a general, efficient, and environmentally benign method for the one-pot cascade synthesis of quinazolin-4(3H)-ones via acceptorless dehydrogenative coupling of o-aminobenzamide with alcohols catalyzed by a simple Ni(II) catalyst, [Ni(MeTAA)], featuring a tetraaza macrocyclic ligand (tetramethyltetraaza[14]annulene (MeTAA)). A wide variety of substituted quinazolin-4(3H)-ones were synthesized in high yields starting from readily available benzyl alcohols and o-aminobenzamides. Several controlled reactions along with deuterium labeling studies were carried out to establish the acceptorless dehydrogenative nature of the reactions.Entities:
Year: 2017 PMID: 28653839 DOI: 10.1021/acs.joc.7b00643
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354