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Flavazol-3-yl acyclo C-nucleosides

Benzo[gJpyrazolo[3,4-b]quinoxalin-3-yl C-Nucleosides benzo[g]flavazol-3-yl Acyclo C-Nucleosides ... [Pg.291]

The only synthetic pathway used so far to prepare these C-nucleosides was the acid-catalyzed cyclodehydration of the alditolyl chains of their acyclo analogs (Section XII,N). Thus, heating l-aryl-3-(D-ara mo-tetritol-l-yl)flavazoles (751) with dilute sulfuric acid gave, stereospecifically, 1-aryl-... [Pg.287]


See other pages where Flavazol-3-yl acyclo C-nucleosides is mentioned: [Pg.289]    [Pg.289]    [Pg.289]    [Pg.289]    [Pg.287]   
See also in sourсe #XX -- [ Pg.70 , Pg.289 ]

See also in sourсe #XX -- [ Pg.70 , Pg.289 ]




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Acyclo-C-nucleosides

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