Stereoselective glycosylations of 2-azido-2-deoxy-glucosides using intermediate sulfonium ions.
about
Sugar Silanes: Versatile Reagents for Stereocontrolled Glycosylation via Intramolecular Aglycone Delivery.Facile chemoenzymatic synthesis of biotinylated heparosan hexasaccharide.Stereoselective assembly of complex oligosaccharides using anomeric sulfonium ions as glycosyl donorsFluorous supported modular synthesis of heparan sulfate oligosaccharides.Mechanism of Glycosylation of Anomeric Sulfonium Ions.Chemical synthesis of glycosylphosphatidylinositol anchors.Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research.Stereoselective glycosylation of glucosamine: the role of the N-protecting group.Modulating glycosylation with exogenous nucleophiles: an overview.Principles of modern solid-phase oligosaccharide synthesis.Design of α-Selective Glycopyranosyl Donors Relying on Remote Anchimeric Assistance.Chemical synthesis and functionalization of clickable glycosylphosphatidylinositol anchors.A synthetic strategy to xylose-containing thioglycoside tri- and tetrasaccharide building blocks corresponding to Cryptococcus neoformans capsular polysaccharide structures.Direct synthesis of diastereomerically pure glycosyl sulfonium salts.Regenerative glycosylation under nucleophilic catalysisAutomated solid-phase synthesis of oligosaccharides containing sialic acids.Total synthesis of an immunomodulatory phosphoglycolipid from thermophilic bacteria.Direct and stereoselective synthesis of alpha-linked 2-deoxyglycosides.Study of the stereoselectivity of 2-azido-2-deoxyglucosyl donors: protecting group effects.Synthesis and biological activity of phosphoglycolipids from Thermus thermophilus.Do glycosyl sulfonium ions engage in neighbouring-group participation? A study of oxathiane glycosyl donors and the basis for their stereoselectivity.A general method for synthesis of GPI anchors illustrated by the total synthesis of the low-molecular-weight antigen from Toxoplasma gondii.Catalytic stereospecific O-glycosylation.Glycosylation intermediates studied using low temperature 1H- and 19F-DOSY NMR: new insight into the activation of trichloroacetimidates.A flexible 1,2-cis α-glycosylation strategy based on in situ adduct transformation.Utilization of bench-stable and readily available nickel(II) triflate for access to 1,2-cis-2-aminoglycosides.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.Acceptor reactivity in the total synthesis of alginate fragments containing α-L-guluronic acid and β-D-mannuronic acid.Reagent Controlled Stereoselective Synthesis of α-Glucans.Synthesis of conjugation-ready zwitterionic oligosaccharides by chemoselective thioglycoside activationA general and convergent synthesis of diverse glycosylphosphatidylinositol glycolipidsEine allgemeine Methode zur Herstellung von GPI-Membranankern am Beispiel der Totalsynthese des “Low-molecular-weight-Antigens” von Toxoplasma gondii
P2860
Q35619813-D05446AE-C6D7-4784-843B-DC3F4D1A69A5Q35754841-3CC33A19-52D4-44BC-91D5-A891F010FBA7Q35964206-CB2BB76B-3BC0-4E21-9426-6AC9C635B085Q36584437-B0BA432C-2D82-4831-BFCD-8FF33B570DE0Q37363866-95BD6EAC-906F-4E2B-A82C-257E11990531Q37418540-82865204-0E23-491D-A6E9-C075D7C94337Q37477221-B31D7CF4-3FEC-4B09-849F-F3C12ACF4DE4Q38023315-7CDA8A69-6372-47A8-A45A-D854B5EAC40EQ38175109-F4C2673D-986E-4BA2-B06E-1D642E5EADB2Q38185269-2B4E12C2-BB1C-4B48-BE74-55968C704D8AQ38703018-044414AC-AE0F-43C4-9A22-64DA7CBB34B0Q39670047-3463C20A-BB4B-4B3E-AF03-B3B54B746248Q40926571-A1CB4F7A-4F2E-4E7C-9CE0-CA422DAD1908Q41819048-DF900EAD-C67A-45C9-840C-D2D4AD628ADEQ41976269-CF850923-F245-4D49-A11F-61B763745D5EQ42529034-D6D078FC-8082-4366-9759-06BAB5F785AEQ43018197-50B1CA58-B130-42E1-AC57-B34EC2AC5BE5Q43193101-DE593A1C-B224-464A-977B-7F7C2846541EQ43445520-91D9D6A3-0A04-4BDF-97AA-52042B029E84Q44168698-78314B82-81A2-4690-9F4D-B36BF4DBF340Q45835674-F77C7283-5762-49F5-96F0-84D43586A1EBQ47356757-85D79316-753C-488F-BE54-6D89177AD945Q48308763-C4D42BBE-0110-4687-B11B-362CB7D890B3Q48311022-073DE67A-BADF-4F51-BEDE-BB21792C5ABCQ48761687-AF1003AA-A159-4048-A3EE-53A3F3768F2FQ49242984-CCC74761-6A9E-49B0-859D-8EEEDBF7DDC3Q53043321-DC52B3E0-DD36-402D-BF9C-06DB3AED4731Q53080060-617FB727-046D-4ACF-896E-2E75DCAC536BQ53511361-5002C592-1D5D-4243-85D5-A30E2A2B5E05Q55278181-31194CB2-620A-41DA-968B-59C8E898BAF8Q57525962-F7584B49-CC39-40BB-9860-0A1F39247AA1Q57760492-C8B9FE13-24B4-45A8-B085-CB9EE6F0AAA0Q57760505-C2A37E56-8D8E-4AA6-A799-C75A22DFF012
P2860
Stereoselective glycosylations of 2-azido-2-deoxy-glucosides using intermediate sulfonium ions.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Stereoselective glycosylations ...... g intermediate sulfonium ions.
@en
type
label
Stereoselective glycosylations ...... g intermediate sulfonium ions.
@en
prefLabel
Stereoselective glycosylations ...... g intermediate sulfonium ions.
@en
P2093
P2860
P356
P1433
P1476
Stereoselective glycosylations ...... g intermediate sulfonium ions.
@en
P2093
Jin-Hwan Kim
Sameer Kawatkar
P2860
P304
P356
10.1021/OL070513B
P407
P577
2007-04-14T00:00:00Z