about
Correlations between nucleophilicities and selectivities in the substitutions of tetrahydropyran acetalsOne-pot syntheses of immunostimulatory glycolipidsCarbohydrate force fieldsSuperarmed and superdisarmed building blocks in expeditious oligosaccharide synthesis.Potent non-nucleoside inhibitors of the measles virus RNA-dependent RNA polymerase complex.The effect of electrostatic interactions on conformational equilibria of multiply substituted tetrahydropyran oxocarbenium ions.Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research.Useful access to enantiomerically pure protected inositols from carbohydrates: the aldohexos-5-uloses route.Design of chemical glycosyl donors: does changing ring conformation influence selectivity/reactivity?A propos of glycosyl cations and the mechanism of chemical glycosylation; the current state of the art.Glycosynthesis in a waterworld: new insight into the molecular basis of transglycosylation in retaining glycoside hydrolases.Conformational Behaviour of Azasugars Based on Mannuronic Acid.Determination of the Influence of Side-Chain Conformation on Glycosylation Selectivity using Conformationally Restricted Donors.Silyl-protective groups influencing the reactivity and selectivity in glycosylations.Benzenesulfonamides: a unique class of chemokine receptor type 4 inhibitors.Stereoselective C-glycoside formation with 2-O-benzyl-4,6-O-benzylidene protected 3-deoxy gluco- and mannopyranoside donors: comparison with O-glycoside formation.Probing the influence of a 4,6-O-acetal on the reactivity of galactopyranosyl donors: verification of the disarming influence of the trans-gauche conformation of C5-C6 bonds.Superarming of glycosyl donors by combined neighboring and conformational effects.Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position.Cation Clock Reactions for the Determination of Relative Reaction Kinetics in Glycosylation Reactions: Applications to Gluco- and Mannopyranosyl Sulfoxide and Trichloroacetimidate Type Donors.The isothiocyanato moiety: an ideal protecting group for the stereoselective synthesis of sialic acid glycosides and subsequent diversification.Absence of Stereodirecting Participation by 2-O-Alkoxycarbonylmethyl Ethers in 4,6-O-Benzylidene-Directed Mannosylation.Does neighboring group participation by non-vicinal esters play a role in glycosylation reactions? Effective probes for the detection of bridging intermediates.Facile oxidative cleavage of 4-O-benzyl ethers with dichlorodicyanoquinone in rhamno- and mannopyranosides.Quantifying the electronic effects of carbohydrate hydroxy groups by using aminosugar models.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 andCatalytic stereospecific O-glycosylation.On the nature of the electronic effect of multiple hydroxyl groups in the 6-membered ring - the effects are additive but steric hindrance plays a role too.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 SialiDirect Experimental Evidence for the High Chemical Reactivity of α- and β-Xylopyranosides Adopting a 2,5B Conformation in Glycosyl Transfer
P2860
Q33683347-1DA03895-CBDE-43DF-8C56-8DCA3E2BD1C1Q34031730-501F6D03-26E1-44F0-974C-D956E2619A73Q34730263-299C58FB-B715-4667-B7D1-E461E462EEEBQ35147955-22FA6B98-6DFA-4ECE-914D-06E5577789C8Q36984136-52115FF4-F263-463F-8EAB-E7A927C1A2D4Q37171066-22B18A91-6DC9-41AD-ADEB-8C291D43A9F1Q37477221-10241265-AD0E-45C6-B5DE-3D414FE7C17EQ37587830-21C4B5FB-8BCB-4318-8F66-25B102CD02FDQ38077932-C207B49D-31EA-4E79-9188-961D130733B9Q38238441-704160CE-ABB1-402C-A04D-3AB1739B0530Q38385154-2E5E1D6F-A342-41C6-8B8B-DAA546C6F5A6Q38931248-CC16B7EF-9C26-4AE0-A5D3-A3DFFD581EA3Q39017696-0FED1D52-EC8D-4184-82B4-B3A455ED6E36Q39147232-1F21E246-9E71-49B7-AF38-90E890283334Q39184086-3D7B87C6-8F8F-4434-B853-9C07E9DB14BDQ41476064-33AD3E76-F4BF-4269-8469-8D00EDEDCC16Q41811288-9F3F11A5-6EE0-4852-9218-CE64D72340EFQ41829763-07553E6A-1079-4EB0-AFE5-6602A326DF50Q41932024-B478B7B2-A99D-4A8A-9558-9ED3123A4257Q42734177-3B83C34A-D17A-4791-B287-EF878571A61CQ43112638-A1039864-0B73-4945-B22F-5B4059848F89Q43122823-82C33EBB-574E-4EE9-A911-9D609242618FQ43145506-2D84D4A4-9701-4335-BAFA-587BAA963F0BQ43210902-6418A177-7E6A-486C-B205-0C9B22C8B686Q44798275-B6BC1923-E24D-4F83-8957-3F8884955D70Q47309853-2DA2A3AA-13AC-4826-9994-195BD206431BQ48308763-2FE49E17-D38A-4A22-879A-0A83C16D757AQ48354901-C62A6B35-D3A8-4BB5-93A8-EFD767CBB235Q55099075-99B133FF-C3E6-4D97-8633-1A3758781E46Q57515384-4747AD59-D643-4969-9074-3EB1765D831E
P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Stereoelectronic substituent effects.
@ast
Stereoelectronic substituent effects.
@en
type
label
Stereoelectronic substituent effects.
@ast
Stereoelectronic substituent effects.
@en
prefLabel
Stereoelectronic substituent effects.
@ast
Stereoelectronic substituent effects.
@en
P356
P1476
Stereoelectronic substituent effects.
@en
P2093
Henrik Helligsø Jensen
Mikael Bols
P304
P356
10.1021/AR050189P
P407
P577
2006-04-01T00:00:00Z