Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis. - Wikidata - wikimedia - TriplyDB

Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

http://www.wikidata.org/entity/Q37035555

about

Fluorous-based small-molecule microarrays for protein, antibody and enzyme screening.A fluorous phosphate protecting group with applications to carbohydrate synthesis.Fluorous-Assisted One-Pot Oligosaccharide Synthesis.Synthesis and applications of a light-fluorous glycosyl donor.Synthesis of fluorous photolabile aldehyde and carbamate and alkyl carbamate protecting groups for carbohydrate-associated amines.Facile synthesis of tetrasaccharide aided by fluorous chemistry toward a dengue virus vaccine.Highly efficient one-pot multienzyme (OPME) synthesis of glycans with fluorous-tag assisted purification.

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Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

http://www.wikidata.org/entity/Q37035555

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

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bilimsel makale

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scientific article published on October 2008

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

@en

Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

@nl

type

label

Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

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Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

@nl

prefLabel

Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

@en

Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

@nl

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P356

J.JFLUCHEM.2008.05.001

P1433

Journal of Fluorine Chemistry

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Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis.

@en

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Aleksandra Zakharova

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

Gisun Park

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

Kwang-Seuk Ko

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

Nicola L Pohl

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P2860

Cycling of O-linked beta-N-acetylglucosamine on nucleocytoplasmic proteins

Heparan sulphate proteoglycans fine-tune mammalian physiology

Automated solid-phase synthesis of oligosaccharides.

Hydrophobically assisted switching phase synthesis: the flexible combination of solid-phase and solution-phase reactions employed for oligosaccharide preparation.

Solution-phase mixture synthesis with double-separation tagging: double demixing of a single mixture provides a stereoisomer library of 16 individual murisolins.

Solution-phase mixture synthesis with fluorous tagging en route: total synthesis of an eight-member stereoisomer library of passifloricins.

Glycan-based interactions involving vertebrate sialic-acid-recognizing proteins.

Exploiting the defensive sugars of HIV-1 for drug and vaccine design.

Synthesis and medical applications of oligosaccharides.

Automated oligosaccharide synthesis.

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978-982

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scholarly article

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10.1016/J.JFLUCHEM.2008.05.001

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10

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129

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2008-10-01T00:00:00Z

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26868577

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19802334

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oligosaccharide

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2613283

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