The dye-sensitized photooxygenation of furanosyl furans easily affords C- or O-glycosides with cis-R,-unsaturated 1,4-dioxo aglycones. The reaction, performed on a ribofuranosyl furan, provides a useful new entry to a novel pyridazine C-nucleoside that can be achieved through a simple one-pot procedure.
Dye-sensitized Photooxygenation of furanosyl Furans; Synthesis of a new Pyridazine C-Nucleoside / Cermola, Flavio; Iesce, MARIA ROSARIA; G., Buonerba. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 70:(2005), pp. 6503-6505.
Dye-sensitized Photooxygenation of furanosyl Furans; Synthesis of a new Pyridazine C-Nucleoside
CERMOLA, FLAVIO;IESCE, MARIA ROSARIA;
2005
Abstract
The dye-sensitized photooxygenation of furanosyl furans easily affords C- or O-glycosides with cis-R,-unsaturated 1,4-dioxo aglycones. The reaction, performed on a ribofuranosyl furan, provides a useful new entry to a novel pyridazine C-nucleoside that can be achieved through a simple one-pot procedure.File in questo prodotto:
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