Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

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Mapping the Reactivity and Selectivity of 2-Azidofucosyl Donors for the Assembly of N-Acetylfucosamine-Containing Bacterial Oligosaccharides.

P2860

Q42156196-3DFD195E-EB21-4B32-897A-4E6B54D6F3DB

P2860

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

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http://www.wikidata.org/entity/Q26770205

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2016 nî lūn-bûn

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2016 թուականի Մարտին հրատարակուած գիտական յօդուած

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2016 թվականի մարտին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

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2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@ast

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@en

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

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Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

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type

Item

label

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@ast

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@en

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@en-gb

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@nl

prefLabel

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@ast

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@en

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@en-gb

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@nl

P1154

2-s2.0-84959902450

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P1433

Chemistry: A European Journal

P1476

Mechanistic Investigations into the Application of Sulfoxides in Carbohydrate Synthesis

@en

P275

Creative Commons Attribution

P2860

Synthesis and reactivity of 4'-deoxypentenosyl disaccharides.

Reactivity-based one-pot total synthesis of fucose GM1 oligosaccharide: a sialylated antigenic epitope of small-cell lung cancer.

Stereocontrolled synthesis of D- and L-beta-rhamnopyranosides with 4-O-6-S-alpha-cyanobenzylidene-protected 6-thiorhamnopyranosyl thioglycosides.

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.

On the influence of the C2-O2 and C3-O3 bonds in 4,6-O-benzylidene-directed beta-mannopyranosylation and alpha-glucopyranosylation.

On the use of 3,5-O-benzylidene and 3,5-O-(di-tert-butylsilylene)-2-O-benzylarabinothiofuranosides and their sulfoxides as glycosyl donors for the synthesis of beta-arabinofuranosides: importance of the activation method.

Cation clock permits distinction between the mechanisms of α- and β-O- and β-C-glycosylation in the mannopyranose series: evidence for the existence of a mannopyranosyl oxocarbenium ion.

Block synthesis of tetra- and hexasaccharides (beta-D-glycero-D-manno-Hep p-(1-->4)-[alpha-l-Rha p-(1-->3)-beta-D-glycero-D-manno-Hep p-(1-->4)]n-alpha-L-Rha p-OMe (n = 1 and 2)) corresponding to multiple repeat units of the glycan from the surface-

Dissecting the mechanisms of a class of chemical glycosylation using primary ¹³C kinetic isotope effects

P304

3916-28

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P31

scholarly article

review article

P356

10.1002/CHEM.201503504

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Robin Brabham

Martin Fascione

Bruce Turnbull

P5530

4968903

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P577

2016-03-14T00:00:00Z

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P6179

1048940010

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P6366

2188896531

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P698

26744250

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P921

Angliavandeniai

sulfoxide

P932

4794778

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P953

92520/