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Magnetic Core-Shell Fe3O4@C-SO3H as an Efficient and Renewable ‘Green Catalyst’ for the Synthesis of O-2,3-Unsaturated Glycopyranosides

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TLDR
A magnetic core-shell solid-acid catalyst Fe3O4@C-SO3H was used for synthesis of O-2,3-unsaturated glycosides through Ferrier rearrangement as mentioned in this paper.
Abstract
A magnetic core-shell solid-acid catalyst Fe3O4@C-SO3H was studied for synthesis of O-2,3-unsaturated glycosides through Ferrier rearrangement. The donors include 3,4,6-tri-O-acetyl- d -glucal and 3,4-di-O-acetyl- l -rhamnal. The acceptors consist of primary alcohols, secondary alcohols, tert-butanol, unsaturated alcohols, halogenated alcohol, sterol, sugars, and phenols. O-2,3-Unsaturated glycosides were obtained rapidly ( 5:1 to 19:1). Moreover, the catalyst can be easily separated from the reaction with an external magnetic force and reused for a minimum of five times without any significant decrease in the yields of the products after every recycle, suggesting it a promising green catalyst in 2,3-unsaturated glycosides syntheses.

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Journal ArticleDOI

Tuning the Chemoselectivity of Silyl Protected Rhamnals by Temperature and Brønsted Acidity: Kinetically Controlled 1,2-Addition vs Thermodynamically Controlled Ferrier Rearrangement

TL;DR: An acidity- and temperature-dependent chemoselective glycosylation of silyl-protected rhamnals with alcohols has been revealed, allowing facile and practical access to both 2,3-unsaturated rhamnosides with excellent yields and high α-stereoselectivity.
Journal ArticleDOI

Eco-friendly synthesis of 5-hydroxymethylfurfural (HMF) and its application to the Ferrier-rearrangement reaction

TL;DR: In this paper, 5-hydroxymethylfurfural was conveniently synthesized by dehydration of D-fructose in a good yield, and it was used to further build bioactive derivatives from 2,3-unsaturated glyco...
Journal ArticleDOI

Progress in the Synthesis of 2,3-unsaturated Glycosides

TL;DR: In this paper, a review summarizes recent advances in the application of various types of catalysts to Ferrier type-I rearrangement reactions, including their synthesis, mechanism, and application of 2, 3-unsaturated glycosides.
Journal ArticleDOI

FeCl3/C as an efficient catalyst for Ferrier rearrangement of 3,4,6-tri-O-Benzyl-D-glucal

TL;DR: FeFeCl3/C was used as an efficient and convenient promoter for glycosylation through Ferrier-type rearrangement of 3,4,6-tri-Obenzyl-D-glucal as mentioned in this paper.
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