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Branched-chain sugars cyclohexanes

Considerable work was done to induce chirality via chiral auxiliaries. Reac tions with aromatic a-ketoesters like phenylglyoxylates 21 and electron-rich al kenes like dioxoles 22 and furan 23 were particularly efficient (Scheme 6). Yield up to 99% and diastereoselectivities higher than 96% have been observed whet 8-phenylmenthol 21a or 2-r-butylcyclohexanol 21b were used as chiral auxiliarie [14-18]. It should be noted that only the exoisomers 24 and 25 were obtained from the reaction of dioxoles 22. Furthermore, the reaction with furan 23 wa regioselective. 24 were suitable intermediates in the synthesis of rare carbohydrate derivatives like branched chain sugars [16], Other heterocyclic compounds liki oxazole 28 [19] and imidazole 29 [20] derivatives as well as acyclic alkenes 3fl 31, and 32 [14,15,21,22] were used as olefinic partners. Numerous cyclohexane derived alcohols [18,21-24] and carbohydrate derivatives [25] were used as chiri... [Pg.184]

All three components are unusual the amino sugar is based on L-glucose streptose is a branched-chain monosaccharide and streptidine is not a sugar at all, but a cyclohexane derivative called an amino cyclitol. [Pg.1019]


See other pages where Branched-chain sugars cyclohexanes is mentioned: [Pg.326]    [Pg.8]    [Pg.1053]    [Pg.182]    [Pg.214]    [Pg.216]    [Pg.303]   
See also in sourсe #XX -- [ Pg.238 ]




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