STEREOCONTROLLED SYNTHESIS OF BETA-2'-DEOXYPYRIMIDINE NUCLEOSIDES VIAINTRAMOLECULAR GLYCOSYLATIONS

Authors
XIA XY WANG JY HAGER MW SISTI N LIOTTA DC
Citation
Xy. Xia et al., STEREOCONTROLLED SYNTHESIS OF BETA-2'-DEOXYPYRIMIDINE NUCLEOSIDES VIAINTRAMOLECULAR GLYCOSYLATIONS, Tetrahedron letters, 38(7), 1997, pp. 1111-1114
Citations number
20
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
7
Year of publication
1997
Pages
1111 - 1114
Database
ISI
SICI code
0040-4039(1997)38:7<1111:SSOBNV>2.0.ZU;2-0
Abstract
A pyrimidine moiety was tethered at the 3'-beta-position of D-threo-fu ranosides. By carefully controlling the reaction conditions, pyrimidin e bases can be delivered to the anomeric center to give of beta-pyrimi dine nucleosides in good yield and with complete stereocontrol. (C) 19 97, Elsevier Science Ltd.