Abstract
A short and efficient synthesis of 1,4,5-trideoxy-1,4-imino- l- xylo-hexitol 2a and 1,4,5-trideoxy-1,4-imino- d- arabino-hexitol 2b is reported using the intramolecular conjugate addition of in situ generated benzylamine to the α,β-unsaturated ester 4 , derived from d-glucose, as the key step.
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