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Amination of meso‐Bromoporphyrins and 9‐Haloanthracenes with Diarylamines Catalyzed by a Palladium–PEPPSI Complex

Amination of meso‐Bromoporphyrins and 9‐Haloanthracenes with Diarylamines Catalyzed by a... Palladium‐catalyzed aminations of bulky aryl halides such as meso‐bromoporphyrins and 9‐haloanthracenes with diarylamines provided efficient syntheses of meso‐aminoporphyrins and 9‐aminoanthracenes. Commercially available and air‐stable Pd‐PEPPSI complexes that have N‐heterocyclic carbene (NHC) as ligands have the highest catalytic activities. The scope of diarylamines is wide enough to use diphenylamine, phenoxazine, phenothiazine, 9,10‐dihydroacrydine, and carbazole. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

Amination of meso‐Bromoporphyrins and 9‐Haloanthracenes with Diarylamines Catalyzed by a Palladium–PEPPSI Complex

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References (53)

Publisher
Wiley
Copyright
Copyright © 2013 Wiley Subscription Services, Inc., A Wiley Company
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201300162
Publisher site
See Article on Publisher Site

Abstract

Palladium‐catalyzed aminations of bulky aryl halides such as meso‐bromoporphyrins and 9‐haloanthracenes with diarylamines provided efficient syntheses of meso‐aminoporphyrins and 9‐aminoanthracenes. Commercially available and air‐stable Pd‐PEPPSI complexes that have N‐heterocyclic carbene (NHC) as ligands have the highest catalytic activities. The scope of diarylamines is wide enough to use diphenylamine, phenoxazine, phenothiazine, 9,10‐dihydroacrydine, and carbazole.

Journal

Asian Journal of Organic ChemistryWiley

Published: Dec 1, 2013

Keywords: ; ; ; ;

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