Selective deprotection of allyl amines using palladium
Lemaire-Audoire, Sandrine; Savignac, Monique; Genêt, Jean-Pierre
1995

Abstract

Mono and diallylamines can be cleaved using Pd(0) catalyst and 2-mercaptobenzoic acid as nucleophile. This methodology has been successfully used for the sequential deprotection of diallylamines. The yields of desallylation are good to quantitative.

Details

Title Selective deprotection of allyl amines using palladium
Author(s) Lemaire-Audoire, Sandrine ; Savignac, Monique ; Genêt, Jean-Pierre
Published in Tetrahedron Letters
Volume 36
Issue 8
Pages 1267-1270
Date 1995
Keywords
DOI https://doi.org/10.1016/0040-4039(95)00003-U
Laboratories LGSA
Record Appears in Scientific production and competences > SB - School of Basic Sciences > SB Archives > LGSA - Laboratory of Glycochemistry and Asymmetric Synthesis
Peer-reviewed publications
Work produced at EPFL
Journal Articles
Published
Record creation date 2005-11-09

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