| Literature DB >> 26399156 |
Nayyef Aljaar1,2, Chandi C Malakar1, Jürgen Conrad1, Uwe Beifuss1.
Abstract
The reaction of 5-substituted 2-nitrosophenols with bromomethyl aryl ketones and related compounds employing K2CO3 as a base in refluxing THF and DMF at 80 °C, respectively, delivers 2-aroylbenzoxazoles in a single step with yields up to 85%. The new method involves an intermolecular nucleophilic substitution followed by intramolecular 1,2-addition and elimination. It allows an efficient and practical access to 2-aroylbenzoxazoles under transition-metal-free conditions.Entities:
Year: 2015 PMID: 26399156 DOI: 10.1021/acs.joc.5b02000
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354