SELENIUM-CONTROLLED STEREOSELECTIVE SYNTHESIS OF 2'-DEOXYNUCLEOSIDES FROM GLYCALS. A FORMAL SYNTHESIS OF AZT

DOI: 10.1016/S0040-4039(00)73571-4

Source and publish data:

Tetrahedron Letters p. 2821 - 2822 (1993)

Update date:2022-08-03

Topics: Catalyst Steric hindrance Stereoselective synthesis Nucleophilic substitution Reagent Chiral Auxiliary Glycals Formal Synthesis Selenium 2'-Deoxynucleosides

Authors:

El-Laghdach, Anas

Diaz, Yolanda

Castillon, Sergio

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Article abstract of DOI:10.1016/S0040-4039(00)73571-4

2'-Deoxynucleosides have been stereoselectively synthesized starting from glycals, using phenylselenyl reagents.Key Words: 2'-Deoxynucleosides, stereoselective glycosylation, glycals.

Full text of DOI:10.1016/S0040-4039(00)73571-4

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