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Synlett 1993; 1993(2): 168-170
DOI: 10.1055/s-1993-22391
DOI: 10.1055/s-1993-22391
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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data processing and storage.Synthesis of Unprotected O-Glycosyl Trichloroacetimidates and Their Reactivity Towards some Glycosyl Acceptors1
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Publikationsverlauf
Publikationsdatum:
19. März 2002 (online)

The preparation of O-unprotected sugars which are activated at the anomeric position with a trichloroacetimidate group is described. Furthermore, some examples illustrate the reactivity of these derivatives as glycosyl donors. They react with different glycosyl acceptors in the presence of an acid catalyst; the yields and the α/β-stereoselectivities depend highly on the reaction conditions.