Methodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.
about
Chemical O-Glycosylations: An OverviewOFox imidates as versatile glycosyl donors for chemical glycosylation.Automated Solution-Phase Synthesis of β-1,4-Mannuronate and β-1,4-Mannan.Twenty Years of Mycobacterial Glycans: Furanosides and Beyond.Design of chemical glycosyl donors: does changing ring conformation influence selectivity/reactivity?Determination of the Influence of Side-Chain Conformation on Glycosylation Selectivity using Conformationally Restricted Donors.Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position.Regenerative glycosylation under nucleophilic catalysisElectrochemical generation of 2,3-oxazolidinone glycosyl triflates as an intermediate for stereoselective glycosylation.Influence of protecting groups on the anomeric equilibrium; case of the 4,6-O-benzylidene acetal in the mannopyranose seriesStereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry.Regiospecific anomerisation of acylated glycosyl azides and benzoylated disaccharides by using TiCl4.Synthesis of Conformationally-Locked cis- and trans-Bicyclo[4.4.0] Mono-, Di-, and Trioxadecane Modifications of Galacto- and Glucopyranose; Experimental Limiting 3JH,H Coupling Constants for the Estimation of Carbohydrate Side Chain Populations andRegenerative Glycosylation.Dehydrative glycosylation with cyclic phosphonium anhydrides.Pyranosides with 2,3-trans carbamate groups: exocyclic or endocyclic cleavage reaction?Significant substituent effect on the anomerization of pyranosides: mechanism of anomerization and synthesis of a 1,2-cis glucosamine oligomer from the 1,2-trans anomer.Glycosylation via remote activation of anomeric leaving groups: development of 2-(2-propylsulfinyl)benzyl glycosides as novel glycosyl donors
P2860
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P2860
Methodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.
description
2011 nî lūn-bûn
@nan
2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Methodology development and ph ...... advancement of glycochemistry.
@ast
Methodology development and ph ...... advancement of glycochemistry.
@en
type
label
Methodology development and ph ...... advancement of glycochemistry.
@ast
Methodology development and ph ...... advancement of glycochemistry.
@en
prefLabel
Methodology development and ph ...... advancement of glycochemistry.
@ast
Methodology development and ph ...... advancement of glycochemistry.
@en
P2860
P356
P1476
Methodology development and ph ...... advancement of glycochemistry.
@en
P2860
P304
P356
10.1021/JO2017026
P407
P50
P577
2011-10-04T00:00:00Z