Abstract
We present methods for β-selective 2-deoxy and 2,6-dideoxyglucosylations of natural products, carbohydrates, and amino acids using bis-thiourea hydrogen-bond-donor catalysts. Disarming ester protecting groups were necessary to counter the high reactivity of 2-deoxyglycosyl electrophiles toward non-stereospecific SN1 pathways. Alcohol and phenol nucleophiles with both base- and acid-sensitive functionalities were compatible with the catalytic protocol, enabling access to a wide array of 2-deoxy-β-O-glucosides.
Supplementary materials
Title
Supporting Information
Description
Experimental procedures and characterization data for cata-lyst synthesis, substrate synthesis and glycosylations. Procedures and data for mechanistic studies and additional substrates not shown in scope figures.
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