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Mannitol 1.6- dibromo-1,6-dideoxy

Tharapautic Function Cancer chemotherapy Chemical Name 1,6-dibromo-1,6-dideoxy-D-mannitol Common Name —... [Pg.1031]

Intramolecular cyclization can also be effected with acyclic intermediates derived from such readily available alditols as D-mannitol. Kuszmann and Vargha63 reported the formation of 2,5-anhydro-l,6-dibromo-l,6-dideoxy-4-0-(methylsulfonyl)-D-glucitol (63), in 73% yield, by boiling 3,5-di-0-acetyl-l,6-dibromo-l,6-dideoxy-2,4-di-0-... [Pg.127]

More recently a group of halogenated sugars have been found to have similar properties to the bifunctional alkylating agents 1. 1,6-Dibromo- 1,6-dideoxy-D-mannitol, for example (DBD, Mitobronitol 10) is now in clinical use, but it is believed to act at least in part by transformation in vivo to the bis epoxide... [Pg.143]

A standard sequence of conversions has been used to convert 1,6-dibromo-1,6-dideoxy-3,4-0-isopropylidene-D-mannitol by chain elongation to the 3,6-diamino-l,4 5,8-dianhydro-L-manno- and L-ido-22... [Pg.168]


See other pages where Mannitol 1.6- dibromo-1,6-dideoxy is mentioned: [Pg.1346]    [Pg.338]    [Pg.380]    [Pg.7]    [Pg.287]    [Pg.257]    [Pg.1346]    [Pg.42]    [Pg.978]    [Pg.338]    [Pg.380]    [Pg.150]    [Pg.168]    [Pg.382]    [Pg.382]    [Pg.1036]    [Pg.1242]    [Pg.178]   
See also in sourсe #XX -- [ Pg.25 , Pg.257 ]




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