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Ribofuranosyl fluoride synthesis

The synthesis of 2,3i5-tri-O-benzyl-yfl-D-ribofuranosyl fluoride and its oC-D-arabinofuranosyl analogue, has been accomplished by the reaction of the tri- -benzylated sugar with 2-fluoro-1-methylpyridin-ium tosylate - triethylamine. [Pg.81]

Purine, 6-bromo-9-/3-D-(2,3,5-tri-0-acetyl)ribofuranosyl-synthesis, 5, 598 Purine, 6-carboxy-reactions, 5, 549 Purine, 8-carboxy-reactions, 5, 549 Purine, 2-chloro-reactions, 5, 561 synthesis, 5, 597 Purine, 6-chloro-alkylation, 5, 529 glycosylation, 5, 529 oxidation, 5, 539 3-oxides reactions, 5, 554 synthesis, 5, 595 reactions, 5, 561, 595 with ammonia, 5, 562 with fluorides, 5, 563 with trimethylamine, 5, 562 9- -D-ribofuranoside synthesis, 5, 560 synthesis, 5, 597, 598 Purine, 8-chloro-amination, 5, 542 Purine, 6-chloro-8-ethoxy-synthesis, 5, 591 Purine, 6-chloro-9-ethyl-dipole moment, 5, 522 Purine, 6-chloro-2-fluoro-riboside... [Pg.758]


See other pages where Ribofuranosyl fluoride synthesis is mentioned: [Pg.225]    [Pg.131]   
See also in sourсe #XX -- [ Pg.48 , Pg.101 ]




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