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α/β-Stereo- and diastereoselective glycosylation with n-pentenyl glycoside donors, promoted by N-iodosuccinimide and catalyzed by chiral Brønsted acid

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ORGANIC & BIOMOLECULAR CHEMISTRY
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ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ob01633a

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This paper describes a method for stereoselective glycosylation using a chiral Bronsted acid, the (+)-isomenthol ester of pentacarbomethoxycyclopentadiene, with n-pentenyl glycosides in the presence of N-iodosuccinimide as the promoter, which offers a chiral recognition of racemic substrates.
A method involving stereoselective glycosylation catalyzed by (+)-isomenthol ester of pentacarbomethoxycyclopentadiene as a chiral Bronsted acid, with n-pentenyl glycosides in the presence of N-iodosuccinimide as the promoter is described; this method offered a chiral recognition of racemic substrates.

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