Issue 17, 2017, Issue in Progress

Coupling of anhydro-aldose tosylhydrazones with hydroxy compounds and carboxylic acids: a new route for the synthesis of C-β-d-glycopyranosylmethyl ethers and esters

Abstract

Cross couplings of O-peracylated 2,6-anhydro-aldose tosylhydrazones (C-(β-D-glycopyranosyl)formaldehyde tosylhydrazones) with alcohols, phenols, and carboxylic acids were studied under thermic or photolytic conditions in the presence of K3PO4 or LiOtBu. The reactions failed with EtOH, BnOH, or tBuOH, however, (CF3)2CHOH, electron poor phenols and carboxylic acids gave the corresponding C-β-D-glycopyranosylmethyl ethers and esters, respectively, representing a new access to these glycomimetic compounds.

Graphical abstract: Coupling of anhydro-aldose tosylhydrazones with hydroxy compounds and carboxylic acids: a new route for the synthesis of C-β-d-glycopyranosylmethyl ethers and esters

Supplementary files

Article information

Article type
Paper
Submitted
24 Nov 2016
Accepted
31 Jan 2017
First published
07 Feb 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 10454-10462

Coupling of anhydro-aldose tosylhydrazones with hydroxy compounds and carboxylic acids: a new route for the synthesis of C-β-D-glycopyranosylmethyl ethers and esters

T. Kaszás, M. Tóth, S. Kun and L. Somsák, RSC Adv., 2017, 7, 10454 DOI: 10.1039/C6RA27282G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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