| Literature DB >> 29364227 |
D Jamin Keith1, Stefan A Marasligiller1, Alexander W Sasse1, Steven D Townsend2.
Abstract
The goal of the following procedure is to provide a demonstration of the one-pot conversion of a 2-azido-1-nitrate-ester to a trichloroacetimidate glycosyl donor. Following azido-nitration of a glycal, the product 2-azido-1-nitrate ester can be hydrolyzed under microwave-assisted irradiation. This transformation is usually achieved using strongly nucleophilic reagents and extended reaction times. Microwave irradiation induces hydrolysis, in the absence of reagents, with short reaction times. Following denitration, the intermediate anomeric alcohol is converted, in the same pot, to the corresponding 2-azido-1-trichloroacetimidate.Entities:
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Year: 2018 PMID: 29364227 PMCID: PMC5908649 DOI: 10.3791/56610
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355