Issue 21, 2019

Fe-Catalyzed decarbonylative cascade reaction of N-aryl cinnamamides with aliphatic aldehydes to construct 3,4-dihydroquinolin-2(1H)-ones

Abstract

A practical Fe-catalyzed decarbonylative cascade reaction of N-aryl cinnamamides with aliphatic aldehydes to provide C3 alkylated 3,4-dihydroquinolin-2(1H)-ones is developed. Aliphatic aldehydes were oxidatively decarbonylated into 1°, 2° and 3° alkyl radicals conveniently, allowing for the subsequent cascade construction of C(sp3)–C(sp3) and C(sp3)–C(sp2) bonds via radical addition and HAS-type cyclization. The importance of the amide linkage and the selectivity of the 6-endo-trig over 5-exo-trig cyclization pathway were elucidated by experimental results and DFT calculations.

Graphical abstract: Fe-Catalyzed decarbonylative cascade reaction of N-aryl cinnamamides with aliphatic aldehydes to construct 3,4-dihydroquinolin-2(1H)-ones

Supplementary files

Article information

Article type
Paper
Submitted
27 Feb 2019
Accepted
01 May 2019
First published
02 May 2019

Org. Biomol. Chem., 2019,17, 5262-5268

Fe-Catalyzed decarbonylative cascade reaction of N-aryl cinnamamides with aliphatic aldehydes to construct 3,4-dihydroquinolin-2(1H)-ones

R. Gao, X. Luan, Z. Xie, L. Yang and Y. Pei, Org. Biomol. Chem., 2019, 17, 5262 DOI: 10.1039/C9OB00492K

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