ALLYLIC ALCOHOL TRANSPOSITIONS IN THE CARBOHYDRATE MOIETY OF PYRIMIDINE NUCLEOSIDES

Authors
IOANNIDIS P SODERMAN P SAMUELSSON B CLASSON B
Citation
P. Ioannidis et al., ALLYLIC ALCOHOL TRANSPOSITIONS IN THE CARBOHYDRATE MOIETY OF PYRIMIDINE NUCLEOSIDES, Tetrahedron letters, 34(18), 1993, pp. 2993-2994
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
18
Year of publication
1993
Pages
2993 - 2994
Database
ISI
SICI code
0040-4039(1993)34:18<2993:AATITC>2.0.ZU;2-8
Abstract
The reagent system chlorodiphenylphosphine, imidazole, and iodine, is shown to be useful in a novel transposition reaction of allylic alcoho ls to provide access to a new class of 2',3'-unsaturated nucleoside an alogues.