Issue 8, 2014

A convenient palladium-catalyzed carbonylative synthesis of 4(3H)-quinazolinones from 2-bromoformanilides and organo nitros with Mo(CO)6 as a multiple promoter

Abstract

A novel and convenient procedure for the synthesis of quinazolinones has been developed. Using 2-bromoformanilides and organo nitros as substrates and Mo(CO)6 as a multiple promoter, the desired products were isolated in moderate to excellent yields in the presence of a palladium catalyst. Here, Mo(CO)6 was not only a CO source, but also a nitro compound reducing reagent and a cyclization promoter.

Graphical abstract: A convenient palladium-catalyzed carbonylative synthesis of 4(3H)-quinazolinones from 2-bromoformanilides and organo nitros with Mo(CO)6 as a multiple promoter

Supplementary files

Article information

Article type
Communication
Submitted
02 May 2014
Accepted
25 Jun 2014
First published
26 Jun 2014

Green Chem., 2014,16, 3763-3767

Author version available

A convenient palladium-catalyzed carbonylative synthesis of 4(3H)-quinazolinones from 2-bromoformanilides and organo nitros with Mo(CO)6 as a multiple promoter

L. He, M. Sharif, H. Neumann, M. Beller and X. Wu, Green Chem., 2014, 16, 3763 DOI: 10.1039/C4GC00801D

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