A New Highly Chemo- and Regioselective Alkoxycarbonylation of Amino Alcohols and polyols

Abstract
The alkoxycarbonylating carbamates 1 and 2 are readily prepared and reacted under mild conditions with polyfunctional substrates, e.g. amino acids, unsymmetrical diols, and unprotected carbohydrates (D-glucosamine and methyl α-D-glucoside), thus affording carbamates or monocarbonates in good yields and with high chemo- and regioselectivity.

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