Issue 73, 2021

Cu(OTf)2 catalyzed Ugi-type reaction of N,O-acetals with isocyanides for the synthesis of pyrrolidinyl and piperidinyl 2-carboxamides

Abstract

The Cu(OTf)2 catalyzed Ugi-type reactions of N,O-acetals with isocyanides have been described for the synthesis of pyrrolidinyl and piperidinyl 2-carboxamides. 4-Hydroxy-5-substituted-prolinamides can be obtained in high diastereoselectivities (2,4-cis/trans > 19 : 1) and a stereoselective model was proposed for 2,4-cis selectivity. Moreover, 4-F-VH 032, a novel analog of the VHL ligand, was conveniently obtained by utilizing the present method.

Graphical abstract: Cu(OTf)2 catalyzed Ugi-type reaction of N,O-acetals with isocyanides for the synthesis of pyrrolidinyl and piperidinyl 2-carboxamides

Supplementary files

Article information

Article type
Communication
Submitted
13 Jun 2021
Accepted
19 Jul 2021
First published
19 Jul 2021

Chem. Commun., 2021,57, 9248-9251

Cu(OTf)2 catalyzed Ugi-type reaction of N,O-acetals with isocyanides for the synthesis of pyrrolidinyl and piperidinyl 2-carboxamides

Z. Mao, X. Nie, Y. Feng, C. Si, B. Wei and G. Lin, Chem. Commun., 2021, 57, 9248 DOI: 10.1039/D1CC03113A

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