alpha-selective sialylations at -78 degrees C in nitrile solvents with a 1-adamantanyl thiosialoside.
about
Advances in the biology and chemistry of sialic acids.Methodology development and physical organic chemistry: a powerful combination for the advancement of glycochemistry.Linear synthesis and immunological properties of a fully synthetic vaccine candidate containing a sialylated MUC1 glycopeptide.Synthesis and immunological study of α-2,9-oligosialic acid conjugates as anti-group C meningitis vaccines.Toward automated oligosaccharide synthesis.Probing the influence of protecting groups on the anomeric equilibrium in sialic acid glycosides with the persistent radical effectExploration of the Oxazolidinthione Protecting System for the Synthesis of Sialic Acid Glycosides.Imposing the trans/gauche conformation on a sialic acid donor with a 5-N,7-O-oxazinanone group: effect on glycosylation stereoselectivity.Stereoselective C-glycoside formation with 2-O-benzyl-4,6-O-benzylidene protected 3-deoxy gluco- and mannopyranoside donors: comparison with O-glycoside formation.Dissecting the influence of oxazolidinones and cyclic carbonates in sialic acid chemistry.Stereoselective synthesis of alpha-keto-deoxy-D-glycero-D-galacto-nonulosonic acid glycosides by means of the 4,5-O-carbonate protecting group.Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position.Synthesis of mucin-type O-glycan probes as aminopropyl glycosides.Influence of protecting groups on the anomeric equilibrium; case of the 4,6-O-benzylidene acetal in the mannopyranose seriesOxidative Deamination of N-Acetyl Neuraminic Acid: Substituent Effects and Mechanism.Influence of the O3 protecting group on stereoselectivity in the preparation of C-mannopyranosides with 4,6-O-benzylidene protected donors.Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deamination.Stereoselective iterative one-pot synthesis of N-glycolylneuraminic acid-containing oligosaccharides.The isothiocyanato moiety: an ideal protecting group for the stereoselective synthesis of sialic acid glycosides and subsequent diversification.Stereoselective Synthesis of the Equatorial Glycosides of Legionaminic Acid.Synthesis of an S-Linked α(2→8) GD3 Antigen and Evaluation of the Immunogenicity of Its Glycoconjugate.A Visible-Light-Promoted O-Glycosylation with a Thioglycoside Donor.Stereoselective Synthesis of 5-epi-α-Sialosides Related to the Pseudaminic Acid Glycosides. Reassessment of the Stereoselectivity of the 5-Azido-5-deacetamidosialyl Thioglycosides and Use of Triflate as Nucleophile in the Zbiral Deamination of Siali
P2860
Q33519629-21CD8E9E-E29A-4658-A0AD-EB91B159BD7AQ35549359-0EBED5AE-4986-4D6A-9B85-6AA32F8CC83BQ35800918-9016A956-31B5-4452-92F8-690BA5E99B4EQ35920353-F38604AB-F86E-4377-852D-B926C2AD3BCCQ37962848-83CE246C-D5A7-4236-B7DD-1489F0CE2A5EQ39044526-4B5DD12C-3C6A-4F09-BE7E-D753FF92B386Q40065968-C581776F-DA83-4125-96CC-C135CE9EA100Q41276894-2030E7DB-8FE4-4522-9C65-F4229CEDD08EQ41476064-F0DAC37B-C62E-439A-AF55-AEFC07255C8FQ41482514-7ADAE9AF-AE14-453B-A3D4-6E1AA5C6F823Q41842610-E03E1599-93F2-4644-91FB-741286193C97Q41932024-80E69C34-968C-4B25-8935-EF4F4EF3238FQ42158841-98849568-AEB1-4489-AD9C-CE2D48968E7FQ42236654-2A96A22C-6479-4995-8AFC-699D2F0FFE9DQ42536038-13260542-C2ED-4E33-9A6F-CE1A64F22791Q42704172-8956670A-A39A-42FF-A16B-2BC20962FEBFQ42789515-D7D1C4CD-F58E-4337-B080-597BC5A844F1Q43069778-6961085C-D101-4B72-8CA6-B2B157DA62CBQ43112638-95DCE70A-8689-4A39-AC3B-A5559804C5B8Q48115807-C7954683-E182-4C78-BC76-082CA48607F9Q51098501-35167FDA-E581-4BB6-A8B8-82DA675D1A2EQ53137102-A827A248-C283-493E-9B86-9C261E25AA52Q55099075-33192618-6882-4440-9BD8-992DCC5BDAF1
P2860
alpha-selective sialylations at -78 degrees C in nitrile solvents with a 1-adamantanyl thiosialoside.
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
alpha-selective sialylations a ...... a 1-adamantanyl thiosialoside.
@en
alpha-selective sialylations a ...... a 1-adamantanyl thiosialoside.
@nl
type
label
alpha-selective sialylations a ...... a 1-adamantanyl thiosialoside.
@en
alpha-selective sialylations a ...... a 1-adamantanyl thiosialoside.
@nl
prefLabel
alpha-selective sialylations a ...... a 1-adamantanyl thiosialoside.
@en
alpha-selective sialylations a ...... a 1-adamantanyl thiosialoside.
@nl
P2860
P356
P1476
alpha-selective sialylations a ...... a 1-adamantanyl thiosialoside.
@en
P2093
P2860
P304
P356
10.1021/JO7012912
P407
P50
P577
2007-09-07T00:00:00Z