Ni/C-catalyzed aminocarbonylation of aryl halides using DMF as an amine source and o-chlorophenyl formate as a CO surrogate and promoter-Reference-Cited by-同舟云学术

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Ni/C-catalyzed aminocarbonylation of aryl halides using DMF as an amine source and o-chlorophenyl formate as a CO surrogate and promoter

Published:2024-05 Issue: Volume:561 Page:114167
ISSN:2468-8231
Container-title:Molecular Catalysis
language:en
Short-container-title:Molecular Catalysis

Author:

Mahajan Vijay P.,Kolekar Yuvraj A.,Bhanage Bhalchandra M.^ORCID

Publisher

Elsevier BV

Reference43 articles.

1. Palladium-catalyzed reductive carbonylation of aryl triflates with synthesis gas;Brennführer;Synlett,2007

2. Pd/C-catalyzed direct formylation of aromatic iodides to aryl aldehydes using carbon dioxide as a C1 resource;Yu;Chem. Commun.,2014

3. Recent developments in palladium-catalyzed carbonylation reactions;Gadge;RSC Adv.,2014

4. An efficient synthesis of weinreb amides and ketones via palladium nanoparticles on ZIF-8 catalyzed carbonylative coupling;Dang;RSC Adv.,2014

5. Pd(OAc)2-catalyzed aminocarbonylation of aryl iodides with aromatic or aliphatic amines in water;Tambade;Synthesis (Stuttg),2008

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