Abstract
Enantiomerically pure R or S 1,3-butanediols were prepared in four steps from L or D threonine by nitrous deamination in the presence of bromide ion followed by esterification and reduction.
Enantiomerically pure R or S 1,3-butanediols were prepared in four steps from L or D threonine by nitrous deamination in the presence of bromide ion followed by esterification and reduction.
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