TY - JOUR
TI - Resolution of 2, 3-Dideoxy-Dl-2-Enopyranos-4-Uloses via chromatographic separation of their diastereomeric O-Tert-Butyloxycarbonyl-L-Alanyl esters. A convenient synthesis of L- and D-Aculose 1.
AU - Constantinou-Kokotou, V.
AU - Couladouros, E.A.
AU - Georgiadis, M.P.
JO - Journal of Carbohydrate Chemistry
PY - 1991
VL - 10
TODO - 5
SP - 749-756
PB - 
SN - 0732-8303, 1532-2327
TODO - 10.1080/07328309108543948
TODO - null
TODO - A simple and effective procedure for the resolution of 2, 3-dideoxy-DL-2-enopyranos-4- uloses is presented. This procedure is based on column chromatographic separation of their diastereomeric 0-(N-rm-butyloxycarbonyl)-L-alanyl esters, followed by mild acidic cleavage of the ester function. L-Aculosc, 2, 3, 6-tridcoxy-L-glycero-hcx-2-cnopyranos-4-ulosc, is also prepared in satisfactory yield. © 1991, Taylor & Francis Group, LLC. All rights reserved.
ER -