Literature DB >> 26399156

Base-Promoted Domino Reaction of 5-Substituted 2-Nitrosophenols with Bromomethyl Aryl Ketones: A Transition-Metal-Free Approach to 2-Aroylbenzoxazoles.

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


  1 in total

Review 1.  The Synthesis and Utility of Metal-Nitrosophenolato Compounds-Highlighting the Baudisch Reaction.

Authors:  Alexander J Nicholls; Thomas Barber; Ian R Baxendale
Journal:  Molecules       Date:  2019-11-06       Impact factor: 4.411

  1 in total

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