NOVEL NUCLEOSIDES VIA INTRAMOLECULAR FUNCTIONALIZATION OF 2,2'-ANHYDROURIDINE DERIVATIVES

Authors
MCGEE DPC SEBESTA DP OROURKE SS MARTINEZ RL JUNG ME PIEKEN WA
Citation
Dpc. Mcgee et al., NOVEL NUCLEOSIDES VIA INTRAMOLECULAR FUNCTIONALIZATION OF 2,2'-ANHYDROURIDINE DERIVATIVES, Tetrahedron letters, 37(12), 1996, pp. 1995-1998
Citations number
27
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
37
Issue
12
Year of publication
1996
Pages
1995 - 1998
Database
ISI
SICI code
0040-4039(1996)37:12<1995:NNVIFO>2.0.ZU;2-D
Abstract
The generation of novel ribonucleoside analogues derived from 2,2'-anh ydrouridines by a 3'-hydroxyl directed intramolecular nucleophilic sub stitution of the 2'-position is described. The methodology allows for the efficient, regio- and stereoselective elaboration of the 2'-positi on, often under exceptionally mild reaction conditions.