Solvent-free, under air selective synthesis of α-glycosides adopting glycosyl chlorides as donors-Reference-Cited by-同舟云学术

Solvent-free, under air selective synthesis of α-glycosides adopting glycosyl chlorides as donors

Published:2020 Issue:27 Volume:18 Page:5157-5163
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Traboni Serena¹²³⁴^ORCID,Vessella Giulia¹²³⁴^ORCID,Bedini Emiliano¹²³⁴^ORCID,Iadonisi Alfonso¹²³⁴

Affiliation:

1. Department of Chemical Sciences

2. University of Naples Federico II

3. I-80126 Naples

4. Italy

Abstract

A solvent-free, under air approach for the highly stereoselective synthesis of α-glycosides from glycosyl chloride donors, promoted by a triethylphosphite, tetrabutylammonium bromide, and N,N-diisopropylethylamine combination.

Funder

Università degli Studi di Napoli Federico II

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01024C

Reference50 articles.

1. Recent developments in chemical oligosaccharide synthesis

2. New Principles for Glycoside-Bond Formation

3. 1,2-cis O-Glycosylation: Methods, Strategies, Principles

4. Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry

5. Advances in Stereoselective 1,2-cis Glycosylation using C-2 Auxiliaries

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Iodine-triphenylphosphine triggers an easy one-pot alpha stereoselective dehydrative glycosylation on hemiacetalic benzylated glycosyl donors;Carbohydrate Research;2023-11

2. A review of the preparation, derivatization and functions of glucosamine and N-acetyl-glucosamine from chitin;Carbohydrate Polymer Technologies and Applications;2023-06

3. A comprehensive solvent-free approach for the esterification and amidation of carboxylic acids mediated by carbodiimides;Tetrahedron;2023-03

4. Expanding the scope of stereoselective α-galactosylation using glycosyl chlorides;Bioorganic & Medicinal Chemistry;2022-11

5. Recent Advances in Stereoselective Chemical O-Glycosylation Reactions;Frontiers in Molecular Biosciences;2022-06-14