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

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scientific article published on October 2008

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2008 (ast) наукова стаття, опублікована в жовтні 2008 (uk) مقالة علمية نشرت في أكتوبر 2008 (ar) scientific article published on October 2008 (en)
publication date	wds:Q37035555-44AD5113-D5ED-41F7-A92B-BAF42DFC9E31
publication date	2008-10-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q37035555-0AAA5C36-15EF-4E60-B9C9-C8B711F6DC96 wds:Q37035555-0DCC0152-EA8D-4F60-87E2-0F3EB08489A1 wds:Q37035555-0F64EEED-08ED-4917-B99E-E56594E02026 wds:Q37035555-29AF0C71-0845-4267-988E-AA99121694FF wds:Q37035555-31A932D6-FDE6-428B-B53C-718F4808B538 wds:Q37035555-3DF30577-C4F6-4769-BF5B-DD23EDDDAC88 wds:Q37035555-4161D202-888F-4E44-8574-B0EB954435B8 wds:Q37035555-4285AA08-0677-4080-AB69-4BD2150BDA97 wds:Q37035555-46C13FF3-CDDF-41CA-8918-A407A93D9B7A wds:Q37035555-4F1E446C-6BC7-4E39-966B-A3F4704D8820 wds:Q37035555-5E75F860-CFDB-470B-83F0-89B10FC035F8 wds:Q37035555-60E2C9CD-C6AC-445D-A76B-09EAA5E20443 wds:Q37035555-852DBBC0-ED89-441C-99AB-8B7D2F2A34AB wds:Q37035555-855B5B05-7AA2-4997-B03A-DF647776D8B8 wds:Q37035555-862F64C1-A46E-4D02-8B4A-77D0919860DD wds:Q37035555-9186BEC4-9DC0-4E00-84A8-49805300B640 wds:Q37035555-928A8C4D-FE2A-4DBB-89A8-64D5EA7578CF wds:Q37035555-93987A05-4E3E-455A-9466-A1DD1AC3E0F9 wds:Q37035555-B87BC53A-29F0-4603-A449-31690E31F2A8 wds:Q37035555-BBF8E577-2B49-4FF7-85F7-D01AEE4F6035 wds:Q37035555-D677EFC9-37ED-4FA4-8439-3E4FBEFEC651 wds:Q37035555-E01D2874-83B5-4864-B257-77199C5C84AA wds:Q37035555-E1881746-CAC9-4BEC-868F-DD1DE2B84DC0 wds:Q37035555-E69D5164-C3D5-4AF2-A25F-A60A93E954F6 wds:Q37035555-F4E79C16-9DB3-4CE7-B7EA-893B6C5C582F wds:Q37035555-F6E60D3F-5E4E-4E5E-9973-7989FA6EE3CF wds:Q37035555-F8E7C4DE-3BEE-4F90-85CB-FC11F7091462
cites work	Glycan-based interactions involving vertebrate sialic-acid-recognizing proteins Fluorous-based carbohydrate microarrays Automated solid-phase synthesis of oligosaccharides Gene synthesis machines: DNA chemistry and its uses Cycling of O-linked beta-N-acetylglucosamine on nucleocytoplasmic proteins Synthesis of fluorous tags for incorporation of reducing sugars into a quantitative microarray platform "Cap-Tag"-Novel Methods for the Rapid Purification of Oligosaccharides Prepared by Automated Solid-Phase Synthesis Financial support from the donors of the Petroleum Research Fund, administered by the ACS (ACS-PRF 34649-G1), Merck (Predoctoral Fello Separation of "light fluorous" reagents and catalysts by fluorous solid-phase extraction: synthesis and study of a family of triarylphosphines bearing linear and branched fluorous tags Fluorous mixture synthesis: a fluorous-tagging strategy for the synthesis and separation of mixtures of organic compounds Froc: a new fluorous protective group for peptide and oligosaccharide synthesis Strategy-Level Separations in Organic Synthesis: From Planning to Practice Exploiting the defensive sugars of HIV-1 for drug and vaccine design Heparan sulphate proteoglycans fine-tune mammalian physiology Toward solution-phase automated iterative synthesis: fluorous-tag assisted solution-phase synthesis of linear and branched mannose oligomers Synthesis and quantitative evaluation of Glycero-D-manno-heptose binding to concanavalin A by fluorous-tag assistance Solid-phase oligosaccharide tagging (SPOT): Validation on glycolipid-derived structures Synthesis and medical applications of oligosaccharides Automated oligosaccharide synthesis 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 Biological modulation by lectins and their ligands in tumor progression and metastasis Oligosaccharide Synthesis on a Fluorous Support Fluorous oligosaccharide synthesis using a novel fluorous protective group Automated synthesis of a protected N-linked glycoprotein core pentasaccharide Rapid oligosaccharide synthesis using a fluorous protective group Oligosaccharide synthesis in microreactors.
author name string	wds:Q37035555-588EA53F-ED11-40C9-AEBD-4EA4E195FE5F wds:Q37035555-7A34F560-2E56-4AB5-B3BB-756F6558932B wds:Q37035555-BCD89126-FC3F-4944-A0F6-D92CC636B4F4 wds:Q37035555-E9BE78DC-59F4-431C-8E21-9961691BB3E4
author name string	Nicola L Pohl Aleksandra Zakharova Gisun Park Kwang-Seuk Ko
rdfs:label	Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (en) Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (nl) Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (ast)
skos:prefLabel	Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (en) Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (nl) Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (ast)
name	Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (en) Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (nl) Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (ast)
title	wds:Q37035555-A7543D43-5115-4108-BBA1-FE4D01ABFF26
title	Mono- Vs. Di-flourous tagged Glucosamines for Iterative Oligosaccharide Synthesis (en)
page(s)	wds:Q37035555-6836422D-85FE-400F-A4B1-AA43BD2C5170
page(s)	978-982
instance of	wds:Q37035555-C5C76E97-43F7-427F-9D8A-1D880D32DCF1
instance of	scholarly article
main subject	wds:Q37035555-4D023B52-B7AB-40AF-87AC-30B4F3040C31
main subject	oligosaccharide
PubMed ID	wds:Q37035555-C857016F-BF34-4A57-8067-877B1E43D917
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19802334

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