Palladium-Catalyzed Ullmann-Type Reductive Homocoupling of Iodoaryl Glycosides
摘要:
A catalytic synthesis of novel biaryl-linked divalent glycosides was achieved using an electroreductive palladium-catalyzed iodoaryl-iodoaryl coupling reaction. This new method was optimized for the synthesis of divalent biaryl-linked mannopyranosides that was subsequently generalized toward several carbohydrate substrates with yields up to 96%.
Synthesis of a small library of bivalent α-d-mannopyranosides for lectin cross-linking
作者:Milan Bergeron-Brlek、Tze Chieh Shiao、M. Corazon Trono、René Roy
DOI:10.1016/j.carres.2011.03.041
日期:2011.9
A small library of bivalent alpha-D-mannopyranosides having rigid linkers was constructed in order to evaluate the effects of inter-saccharide distances upon multivalent binding interactions with plant and bacterial lectins. To this end, iodoaryl and propargyl alpha-D-mannopyranosides were synthesized and the former treated with TMS-acetylene under palladium chemistry to provide their corresponding ethynylaryl derivatives. A library of 15 dimeric members was then obtained using Lewis acid catalyzed glycosidation, aryl-aryl homocoupling, transition metal catalyzed Sonogashira cross-coupling reactions, and oxidative Glaser homocoupling. (C) 2011 Elsevier Ltd. All rights reserved.
Palladium-Catalyzed Ullmann-Type Reductive Homocoupling of Iodoaryl Glycosides
作者:Milan Bergeron-Brlek、Denis Giguère、Tze Chieh Shiao、Catherine Saucier、René Roy
DOI:10.1021/jo2025652
日期:2012.3.16
A catalytic synthesis of novel biaryl-linked divalent glycosides was achieved using an electroreductive palladium-catalyzed iodoaryl-iodoaryl coupling reaction. This new method was optimized for the synthesis of divalent biaryl-linked mannopyranosides that was subsequently generalized toward several carbohydrate substrates with yields up to 96%.