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Decitols

It is evident that syntheses of the Lespieau type can lead to a great number of polyhydroxy compounds. Wiemann has prepared compounds such as CHsCH2(CHOH)6CH2CH3, which he calls diethyl mannitol. It would seem better to designate this substance a tetra-desoxy decitol or decane hexol since its configuration is not known with certainty. Apparently this type of synthesis leads to symmetrical arrangements of hydroxyl groups, since allitol, dulcitol and D,L-mannitol are the only hexitols that were identified as products. [Pg.217]

Four octitols, one nonitol, one decitol, and one dodecitol have been de-described. Of these only the configurations of the octitols are completely known. None occurs naturally. [Pg.256]

Alditols, Cyclitols and Derivatives Thereof. - 2,5 3,4-Dianhydro-D-altritol, 2,5-aohydro-3,4-0-(l,2-ethanediyl)-D mannitol, pentaerythritol tetraacetate, ribitol tetraacetate, xylitol tetraacetate, D-arabinitol tetraacetate, D, L-arabinitol tetraacetate, 2,4 3,5-di-0-isopropylidene-D-mannitol, 2 hexa-O-acetyl-D-mannitol, allitol hexaacetate, D-mannitol hexaacetate, D, L-mannitol hexaacetate, D-iditol hexaacetate, D, L-iditol hexaacetate, D, L-glucitol hexaacetate, D, L-altritol hexaacetate, L-galacto-D-galacto-decitol (which is C2-symmetric), 5 6-0-benzyl-2,3-0-[(S)-caniphanylidene]-l,4,5-tris-0-pivaloyl-D-myo-inositol, 6D-3,6-di-0-benzyl-l-0-[(S)-camphanyl]-2-deoxy-2,2-difluoro-4,5-0-isopropylidene- y< -inositol, cyclopentane 28. ... [Pg.281]

Further studies have been reported by Brimacombe s group on the synthesis of decitol derivatives previously-described procedures have been used to prepare D-altro-D-galacto-decitol together with... [Pg.172]


See other pages where Decitols is mentioned: [Pg.223]    [Pg.15]    [Pg.223]    [Pg.167]    [Pg.168]    [Pg.327]    [Pg.256]    [Pg.258]    [Pg.294]    [Pg.223]    [Pg.15]    [Pg.223]    [Pg.167]    [Pg.168]    [Pg.327]    [Pg.256]    [Pg.258]    [Pg.294]   
See also in sourсe #XX -- [ Pg.257 ]




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Decitol

Decitol

Octitols, Nonitols, and Decitols

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