Palladium-catalyzed allylic amination: a powerful tool for the enantioselective synthesis of acyclic nucleoside phosphonates-Reference-Cited by-同舟云学术

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

Published:2017 Issue:34 Volume:15 Page:7227-7234
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Azzouz Mariam¹²³⁴⁵,Soriano Sébastien¹²³⁴⁵,Escudero-Casao Margarita¹²³⁴⁵^ORCID,Matheu M. Isabel¹²³⁴⁵^ORCID,Castillón Sergio¹²³⁴⁵^ORCID,Díaz Yolanda¹²³⁴⁵^ORCID

Affiliation:

1. Departament de Química Analítica I Química Orgànica

2. Facultat de Química

3. Universitat Rovira i Virgili

4. 43007 Tarragona

5. Spain

Abstract

Acyclic nucleoside phosphonate were prepared in high yield and up to 92% ee using an enantioselective palladium-catalyzed allylic substitution.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01478C

Reference38 articles.

1. Acyclic nucleoside phosphonates: An unfinished story

2. M. Krecmerova , in Herpesviridae—A Look into This Unique Family of Viruses, ed. G. D. Magel and S. Tyring, INTECH, 2012, ch. 11, p. 245

3. The acyclic nucleoside phosphonates from inception to clinical use: Historical perspective

4. Acyclic nucleoside phosphonates: a key class of antiviral drugs

5. Phosphonomethoxyalkyl Analogs of Nucleotides

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