Additive-Controlled Stereoselective Glycosylations of Oxazolidinone-Protected Glucosamine and Galactosamine Thioglycoside Donors Based on Preactivation Protocol

Synlett - Germany
doi 10.1055/s-0030-1258557
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Georg Thieme Verlag KG

Related search

Direct Α-Selective Glycosylations of Acetyl-Protected 2-Deoxy- And 2,6-Dideoxythioglycosides by Preactivation Protocol

Synlett
Organic Chemistry
2010English

Syntheses of LewisXand Dimeric LewisX: Construction of Branched Oligosaccharides by a Combination of Preactivation and Reactivity Based Chemoselective One-Pot Glycosylations

Journal of Organic Chemistry
Organic Chemistry
2007English

Remote Participation of Protecting Groups at Remote Positions of Donors in Glycosylations

Trends in Glycoscience and Glycotechnology
BiochemistryOrganic Chemistry
2011English

Development of an Additive-Controlled, SmI2-mediated Stereoselective Sequence: Telescoped Spirocyclisation, Lactone Reduction and Peterson Elimination

Beilstein Journal of Organic Chemistry
Organic Chemistry
2013English

A Method for the Determination of D-Galactosamine in the Presence of D-Glucosamine

Biochemical Journal
1963English

A Convenient Synthesis of S-Glycosyl Donors of D-Glucose and O-Glycosylations Involving the New Reagent.

Chemical and Pharmaceutical Bulletin
MedicineDrug DiscoveryChemistry
1990English

Stereoselective Synthesis of Protected Peptides Containing an Anti Beta-Hydroxy Tyrosine

European Journal of Organic Chemistry
Organic ChemistryTheoretical ChemistryPhysical
2019English

Water-Mediated Catalyst Preactivation: An Efficient Protocol for C−N Cross-Coupling Reactions

Organic Letters
BiochemistryOrganic ChemistryTheoretical ChemistryPhysical
2008English

Controlled Thiolate-Protected Gold and Alloy Clusters

2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy