Premium
A Stereoselective Approach to Isoxazolidinyl Nucleosides
Author(s) -
Chiacchio Ugo,
Corsaro Antonino,
Iannazzo Daniela,
Piperno Anna,
Procopio Antonio,
Rescifina Antonio,
Romeo Giovanni,
Romeo Roberto
Publication year - 2001
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/1099-0690(200105)2001:10<1893::aid-ejoc1893>3.0.co;2-k
Subject(s) - chemistry , stereoselectivity , combinatorial chemistry , stereochemistry , organic chemistry , catalysis
A stereoselective approach towards isoxazolidinyl nucleosides has been designed. The 1,3‐dipolar cycloaddition of a C ‐chiral nitrone with purine and pyrimidine nucleobases produces thymidine and adenine N , O ‐nucleosides, in enantiomerically pure forms.