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Selective palladium-catalysed carbonylations of dichloroquinoline and simple dichloropyridines

✍ Scribed by Douja Najiba; Jean-François Carpentier; Yves Castanet; Christophe Biot; Jacques Brocard; André Mortreux

Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
218 KB
Volume
40
Category
Article
ISSN
0040-4039

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✦ Synopsis

Dichloroquinoline and some dichloropyridines undergo selective alkoxycarbonylation in the presence of carbon monoxide, an alcohol and PdCI2(PPh3) 2 as a catalyst, affording chloro-monoester and/or diesters in good yields under selected reaction conditions.

📜 SIMILAR VOLUMES

ChemInform Abstract: Selective Palladium
ChemInform Abstract: Selective Palladium-Catalyzed Carbonylations of Dichloroquinoline and Simple Dichloropyridines.
✍ Douja Najiba; Jean-Francois Carpentier; Yves Castanet; Christophe Biot; Jacques 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

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Microwave-assisted palladium-catalysed c
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Mo(CO) 6 acts as a source of carbon monoxide for the palladium-catalysed, microwave-assisted, carbonylative coupling of aryl or heteroaryl halides with sulfamide nucleophiles to yield aryl and heteroaryl acyl sulfamides.