Regioselective Alkylation and Acylation of Methyl, 2,6-Dideoxyhexo-Pyranosides Via Their Stannylene Acetals: Key Step for the Synthesis of Daunosamine and Related Amino-Sugars
- 1 May 1987
- journal article
- research article
- Published by Taylor & Francis in Journal of Carbohydrate Chemistry
- Vol. 6 (2) , 221-229
- https://doi.org/10.1080/07328308708058872
Abstract
Synthetic intermediates for the preparation of 3-amino-2,3,6 (or 4-amino-2,4,6)-trideoxy-L-hexopyranosides, sugar moieties of anthracycline antibiotics, were selectively obtained from stannylene acetals of methyl 2,6-dideoxy-α-L-lyxo and arabino-hexopyranosides.This publication has 15 references indexed in Scilit:
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