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Carbohydr Res. 2013 Dec 15;382:36-42. doi: 10.1016/j.carres.2013.09.011. Epub 2013 Oct 10.

Combined Lewis acid and Brønsted acid-mediated reactivity of glycosyl trichloroacetimidate donors.

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1
Department of Chemistry, Yale University, PO Box 208107, New Haven, CT 06520-8107, United States.

Abstract

Biomimetic conditions for a synthetic glycosylation reaction, inspired by the highly conserved functionality of carbohydrate active enzymes, were explored. At the outset, we sought to generate proof of principle for this approach to developing catalytic systems for glycosylation. However, control reactions and subsequent kinetic studies showed that a stoichiometric, irreversible reaction of the catalyst and glycosyl donor was occurring, with a remarkable rate variance depending upon the structure of the carboxylic acid. It was subsequently found that a combination of Brønsted acid (carboxylic acid) and Lewis acid (MgBr2) was unique in catalyzing the desired glycosylation reaction. Thus, it was concluded that the two acids act synergistically to catalyze the desired transformation. The role of the catalytic components was tested with a number of control reactions and based on these studies a mechanism is proposed herein.

KEYWORDS:

Biomimetic; Catalytic; Glycosylation; Magnesium; Schmidt

PMID:
24177201
DOI:
10.1016/j.carres.2013.09.011
[Indexed for MEDLINE]
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