Intramolecular glycosylation to form 4-methoxy-2,6-dioxopyrimidine nucleosides via O6,5'-cyclonucleosides

Article abstract of DOI:10.1080/07328319908044616

Lewis-acid promoted intramolecular N1 glycosylation to form the novel O⁶,5'-cyclonucleoside 1a occurs in high yield from the corresponding acyclic thiophenyl-glycoside 12. The relative stability of the 06,5' tether compared with O²,5

Full text of DOI:10.1080/07328319908044616

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Intramolecular Glycosylation to Form
4-Methoxy-2,6-Dioxopyrimidine
Nucleosides via O6,5′-Cyclonucleosides
Claire Castro a , Chuan Chen a & Michael E. Jung b
a Department of Chemistry , University of San Francisco , San
Francisco, CA, 94117-1080
b Department of Chemistry and Biochemistry , University of
California , Los Angeles, CA, 90095-1569
Published online: 04 Oct 2006.
To cite this article: Claire Castro , Chuan Chen & Michael E. Jung (1999) Intramolecular Glycosylation
to Form 4-Methoxy-2,6-Dioxopyrimidine Nucleosides via O6,5′-Cyclonucleosides, Nucleosides and
Nucleotides, 18:11-12, 2415-2423, DOI: 10.1080/07328319908044616
To link to this article: http://dx.doi.org/10.1080/07328319908044616
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