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One‐Pot Synthesis of 2‐Arylbenzoxazoles by Gas‐Free Carbonylation using Dicobalt Octacarbonyl as a Solid Carbon Monoxide Source

One‐Pot Synthesis of 2‐Arylbenzoxazoles by Gas‐Free Carbonylation using Dicobalt Octacarbonyl as... A simple, mild, and facile carbonylation procedure to synthesise 2‐arylbenzoxazole derivatives using dicobalt octacarbonyl [Co2(CO)8] as an in situ carbon monoxide source is described. This method is tolerant of a variety of functional groups and the compounds are obtained in high to excellent yields. Moreover, the reaction is performed in one‐pot with a simple workup procedure. The choice of catalytic system as well as base is important in order to ensure a high yield and chemoselectivity in the reaction. Both electron‐rich and electron‐deficient aryl bromides worked well in this reaction. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

One‐Pot Synthesis of 2‐Arylbenzoxazoles by Gas‐Free Carbonylation using Dicobalt Octacarbonyl as a Solid Carbon Monoxide Source

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References (39)

Publisher
Wiley
Copyright
Copyright © 2015 Wiley Subscription Services, Inc., A Wiley Company
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201402252
Publisher site
See Article on Publisher Site

Abstract

A simple, mild, and facile carbonylation procedure to synthesise 2‐arylbenzoxazole derivatives using dicobalt octacarbonyl [Co2(CO)8] as an in situ carbon monoxide source is described. This method is tolerant of a variety of functional groups and the compounds are obtained in high to excellent yields. Moreover, the reaction is performed in one‐pot with a simple workup procedure. The choice of catalytic system as well as base is important in order to ensure a high yield and chemoselectivity in the reaction. Both electron‐rich and electron‐deficient aryl bromides worked well in this reaction.

Journal

Asian Journal of Organic ChemistryWiley

Published: Apr 1, 2015

Keywords: ; ; ; ; ;

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