A new and convenient approach for the synthesis of ribo- and 2 '-deoxyribo-beta-L-furanonucleosides starting from beta-L-xylofuranonucleosides

Citation
V. Boudou et al., A new and convenient approach for the synthesis of ribo- and 2 '-deoxyribo-beta-L-furanonucleosides starting from beta-L-xylofuranonucleosides, NUCLEOS NUC, 18(4-5), 1999, pp. 607-609
Citations number
4
Categorie Soggetti
Biochemistry & Biophysics
Journal title
NUCLEOSIDES & NUCLEOTIDES
ISSN journal
07328311 → ACNP
Volume
18
Issue
4-5
Year of publication
1999
Pages
607 - 609
Database
ISI
SICI code
0732-8311(1999)18:4-5<607:ANACAF>2.0.ZU;2-Q
Abstract
Ribo- and 2'-deoxyribo-beta-L-furanosyladenine have been synthesized. Altho ugh these compounds have been already reported in the literature, it seemed to us that a more convenient approach for their synthesis deserved to be d eveloped. Intramolecular substitution as well as Mitsunobu reaction were us ed to invert the configuration of carbon 3' of starting beta-L-xylofuranosy l intermediates.