Issue 82, 2020

Metal-free spirocyclization of N-arylpropiolamides with glyoxylic acids: access to complex azaspiro-fused tricycles

Abstract

A metal-free oxidative cascade acylation and dearomatization of N-(p-methoxyaryl)propiolamides was achieved via K2S2O8 mediated decarboxylation of α-oxocarboxylic acids under operationally simple conditions to access azaspiro[4,5]-trienones in good to excellent yields. Furthermore, the utility of the protocol was illustrated in a one-pot reaction sequence consisting of Ugi-reaction/spirocyclization/aza-Michael transformation for the construction of complex tricyclic cores having quaternary spirocenters.

Graphical abstract: Metal-free spirocyclization of N-arylpropiolamides with glyoxylic acids: access to complex azaspiro-fused tricycles

Supplementary files

Article information

Article type
Communication
Submitted
12 Jul 2020
Accepted
03 Sep 2020
First published
03 Sep 2020

Chem. Commun., 2020,56, 12367-12370

Metal-free spirocyclization of N-arylpropiolamides with glyoxylic acids: access to complex azaspiro-fused tricycles

A. M. Nair, A. H. Shinde, S. Kumar and C. M. R. Volla, Chem. Commun., 2020, 56, 12367 DOI: 10.1039/D0CC04800C

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