@article{3027659,
    title = "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.",
    author = "Constantinou-Kokotou, V. and Couladouros, E.A. and Georgiadis, M.P.",
    journal = "Journal of Carbohydrate Chemistry",
    year = "1991",
    volume = "10",
    number = "5",
    pages = "749-756",
    issn = "0732-8303, 1532-2327",
    doi = "10.1080/07328309108543948",
    abstract = "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."
}