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Tetra-O-benzoyl-a-D-mannopyranosyl bromide

Similarly, the mannopyranosyl analog (346) was synthesized by condensation of di-O-isopropylidene-a-DL-carba-mannopyranose (349) with 348. The other isomer (347) was obtained by reaction of 278 with tetra-O-benzoyl-a-D-mannopyranosyl bromide (350). The four carba-glucopyrano-syl D-mannopyranosides, including 346 and 347, show no antiviral activity. [Pg.73]

See other pages where Tetra-O-benzoyl-a-D-mannopyranosyl bromide is mentioned: [Pg.701] [Pg.1108] [Pg.1162]

See also in sourсe #XX -- [ Pg.48 , Pg.73 ]

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A-benzoyl

Benzoyl bromide

D 5-benzoyl

Mannopyranosylations