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Cyanohydrin Formation and Chain Extension

The reaction is used for the chain extension of aldoses in the synthesis of new or unusual sugars In this case the starting material l arabinose is an abundant natural product and possesses the correct configurations at its three chirality centers for elaboration to the relatively rare l enantiomers of glucose and mannose After cyanohydrin formation the cyano groups are converted to aldehyde functions by hydrogenation m aqueous solution Under these conditions —C=N is reduced to —CH=NH and hydrolyzes rapidly to —CH=0 Use of a poisoned palladium on barium sulfate catalyst prevents further reduction to the alditols... [Pg.1056]


See other pages where Cyanohydrin Formation and Chain Extension is mentioned: [Pg.1055]    [Pg.1055]    [Pg.1055]    [Pg.1062]    [Pg.1062]    [Pg.1054]    [Pg.1055]    [Pg.1055]    [Pg.1055]    [Pg.1062]    [Pg.1062]    [Pg.1054]    [Pg.1001]    [Pg.1001]    [Pg.1001]    [Pg.1001]    [Pg.198]   


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Chain extensibility

Chain extension

Chain formation

Cyanohydrin formation

Cyanohydrine

Cyanohydrins

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