The Staudinger/aza-Wittig/Grignard reaction as key step for the concise synthesis of 1-C-Alkyl-iminoalditol glycomimetics
文摘
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The Staudinger/aza-Wittig Grignard reaction cascade is a concise synthetic method for the synthesis of biologically active 1-C-alkyl iminoalditol glycomimetics.

A concise synthetic approach to biologically active 1-C-alkyl iminoalditol glycomimetics: The Staudinger/aza-Wittig Grignard reaction cascade.

The stereoselective control of C-1 alkyl substitution can be controlled by the choice of protecting groups at the sugar substrate as well as the nature of the nucleophilic Grignard reagent in the Staudinger/aza-Wittig Grignard reaction cascade.

Compounds exhibit selective b-glucosidase inhibition.

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