Issue 34, 2017

Palladium-catalyzed allylic amination: a powerful tool for the enantioselective synthesis of acyclic nucleoside phosphonates

Abstract

Acyclic nucleoside phosphonates have been prepared in a straightforward manner and in high yields by an enantioselective palladium-catalyzed allylic substitution involving nucleic bases as nucleophiles followed by cross-metathesis reaction with diethyl allylphosphonate.

Graphical abstract: Palladium-catalyzed allylic amination: a powerful tool for the enantioselective synthesis of acyclic nucleoside phosphonates

Supplementary files

Article information

Article type
Paper
Submitted
19 Jun 2017
Accepted
07 Aug 2017
First published
10 Aug 2017
This article is Open Access
Creative Commons BY-NC license

Org. Biomol. Chem., 2017,15, 7227-7234

Palladium-catalyzed allylic amination: a powerful tool for the enantioselective synthesis of acyclic nucleoside phosphonates

M. Azzouz, S. Soriano, M. Escudero-Casao, M. I. Matheu, S. Castillón and Y. Díaz, Org. Biomol. Chem., 2017, 15, 7227 DOI: 10.1039/C7OB01478C

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