A five-step synthesis of O,N-protected (+)-3-Deoxynojirimycin from N-Boc L-serinal acetonide employing 2-acetylthiazole as a mesked alpha-hydroxy propanal beta-anion synthon is described.
A divergent route to nojirimycin analogues from L-serinal and 2-acetylthiazole
DONDONI, Alessandro;FANTIN, Giancarlo;FOGAGNOLO, Marco;
1990
Abstract
A five-step synthesis of O,N-protected (+)-3-Deoxynojirimycin from N-Boc L-serinal acetonide employing 2-acetylthiazole as a mesked alpha-hydroxy propanal beta-anion synthon is described.File in questo prodotto:
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