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Three-step synthesis of l-ido-1-deoxynojirimycin derivatives by reductive amination in water, “borrowing hydrogen” under neat conditions and deprotection†
Kai Zhao,Gang Zhou,Huifang Nie,Weiping Chen
Organic & Biomolecular Chemistry Pub Date : 09/08/2016 00:00:00 , DOI:10.1039/C6OB01864E
Abstract

In this communication, we describe a three-step synthesis of L-ido-1-deoxynojirimycin derivatives starting from readily available 2,3,4,6-tetra-O-benzyl-D-glucopyranose via Ir-catalyzed reductive amination in water, “borrowing hydrogen” under neat conditions, and Pd-catalyzed debenzylation.

Graphical abstract: Three-step synthesis of l-ido-1-deoxynojirimycin derivatives by reductive amination in water, “borrowing hydrogen” under neat conditions and deprotection
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