Microwave‐Assisted Decarbonylative Coupling Reaction of o‐Halobenzamides for Phenanthridinone Synthesis | Zendy

Chen Xuwen | Zendy; Liu Yunyun | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Microwave‐Assisted Decarbonylative Coupling Reaction of o‐Halobenzamides for Phenanthridinone Synthesis

Author(s) -

Chen Xuwen,

Liu Yunyun

Publication year - 2018

Publication title -

chemistryselect

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.437

H-Index - 34

ISSN - 2365-6549

DOI - 10.1002/slct.201801441

Subject(s) - annulation , catalysis , palladium , coupling (piping) , coupling reaction , amide , chemistry , microwave , combinatorial chemistry , photochemistry , organic chemistry , materials science , physics , quantum mechanics , metallurgy

The microwave assisted synthesis of valuable phenanthridinones via the homo‐annulation of o‐halobenzamides is realized via palladium catalysis. The formation of the products involves in the reductive coupling of aromatic C−X (X=Br, I) bond and the decarbonylative coupling of amide. With this method, a broad array of free NH and N ‐substituted phenanthridinones have been rapidly synthesized.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research