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P-Phenylbenzoyl chloride

HYDROXYL GROUPS ( Bntyldimethyl-cblorosilane. Dimethyl f-buiylchlorosilane. p-Phenylbenzoyl chloride. 9-Phenyl-9-hy-droxyanthrone. NJ4 -Tetramothyl-diamidophosphorochloridate. 0 J-Tri-diloroethyl chloroformate. [Pg.587]

Lombardo methylenation (zinc-dibromomethane-titanium tetrachloride) of methyl 2-deoxy-5-0-(4-phenylbenzoyl)-P-D-g/ycero-pent-3-uloside, followed by dihydroxylation, gave the 3-C-hydroxymethyl derivative 7 (R = 4-phenylbenzoyl) exclusively. A ran of other 2-deoxypentuloses was also subjected to a similar course of reactions, but erally resulted in the formation of epimers during the dihydroxylation step. The hydroxymethyl group was further transformed first with tosyl chloride to the tosylate which was displaced with adenine or thymine to yield nucleoside analogues. ... [Pg.192]

See other pages where P-Phenylbenzoyl chloride is mentioned: [Pg.29]    [Pg.180]    [Pg.339]    [Pg.376]    [Pg.376]    [Pg.339]    [Pg.355]    [Pg.192]    [Pg.192]    [Pg.53]    [Pg.56]    [Pg.145]    [Pg.145]    [Pg.29]    [Pg.180]    [Pg.339]    [Pg.376]    [Pg.376]    [Pg.339]    [Pg.355]    [Pg.192]    [Pg.192]    [Pg.53]    [Pg.56]    [Pg.145]    [Pg.145]    [Pg.331]   
See also in sourсe #XX -- [ Pg.376 ]

See also in sourсe #XX -- [ Pg.376 ]



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