Literature DB >> 21218234

Chemospecific and ligand free CuI catalysed heterogeneous N-arylation of amines with diheteroaryl halides at room temperature.

Sanjeev K Verma1, B N Acharya, M P Kaushik.   

Abstract

A ligand free, copper-catalyzed N-arylation reaction of amines with diheteroaryl halides in heterogeneous medium at room temperature has been developed. The protocol is very effective for low boiling amines and useful for amines available in aqueous solution. The reaction gives chemospecific arylation of amines with diheteroaryl halides in the mixture monoheteroaryl halides, diheteroaryl halides and carbocyclic aryl halides. The reaction is also chemospecific with respect to arylation of aliphatic amines. Monoarylated piperazines were also synthesized at room temperature following this protocol.

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Year:  2011        PMID: 21218234     DOI: 10.1039/c0ob00859a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Pd-Catalyzed Synthesis of Piperazine Scaffolds Under Aerobic and Solvent-Free Conditions.

Authors:  Sean W Reilly; Robert H Mach
Journal:  Org Lett       Date:  2016-10-13       Impact factor: 6.005

2.  Intriguing enigma of nitrobenzofuroxan's 'Sphinx': Boulton-Katritzky rearrangement or unusual evidence of the N-1/N-3-oxide rearrangement?

Authors:  Gabriele Micheletti; Leonardo Iannuzzo; Matteo Calvaresi; Silvia Bordoni; Dario Telese; Elena Chugunova; Carla Boga
Journal:  RSC Adv       Date:  2020-09-18       Impact factor: 4.036

  2 in total

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