About: Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents

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About: Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1999

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1999 (uk) article scientifique publié en 1999 (fr) im Dezember 1999 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 1999 (ast) scientific article published on 01 December 1999 (en)
publication date	wds:Q73846083-61262E83-D842-4EC8-A123-83F580A2EAF9
publication date	1999-12-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73846083-55EB1A09-B275-497C-B685-B925D57177C2 wds:Q73846083-5BFEC0C7-5E07-4C8F-8C50-13F0F19AF069 wds:Q73846083-989570FF-17DB-4B65-9E9C-4719E6632985 wds:Q73846083-F99EE98D-2997-474C-8261-145264DF4DAD
author name string	P H Seeberger L G Melean O J Plante R B Andrade
rdfs:label	Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents (en) Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents (nl)
skos:prefLabel	Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents (en) Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents (nl)
name	Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents (en) Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents (nl)
title	wds:Q73846083-735CEC56-9506-4E52-8482-074585578B6B
title	Solid-phase oligosaccharide synthesis: preparation of complex structures using a novel linker and different glycosylating agents (en)
page(s)	wds:Q73846083-480ECE10-2A39-451B-99B2-C30D267B9803
page(s)	1811-1814
instance of	wds:Q73846083-54AB4A40-5308-4AF5-9CE9-C8C0C0FBC004
instance of	scholarly article
PubMed ID	wds:Q73846083-1BBB237E-3B13-427D-90A7-BFE7B7E8547A
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10836038
PubMed ID	10836038
published in	wds:Q73846083-A03D31F0-3600-4C30-AB55-FF61B148621C
published in	Organic Letters
issue	wds:Q73846083-D67BD3D7-9C1E-4007-8072-B3592A087934
volume	wds:Q73846083-AE0CDCD0-4F83-4FEC-9679-4198FBA75FF8
issue	11
volume	1
DOI	wds:Q73846083-D7A997EE-9532-4DA9-9DB4-A4C74645AB38
DOI	http://dx.doi.org/10.1021/OL991071%2B
DOI	10.1021/OL991071+
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73846083
is cites work of	Multisite and multivalent binding between cyanovirin-N and branched oligomannosides: calorimetric and NMR characterization Synthesis and medical applications of oligosaccharides Development of an automated oligosaccharide synthesizer Toward the automated solid-phase synthesis of oligoglucosamines: systematic evaluation of glycosyl phosphate and glycosyl trichloroacetimidate building blocks Imidazolium cation supported solution-phase assembly of homolinear alpha(1-->6)-linked octamannoside: an efficient alternate approach for oligosaccharide synthesis Automated Chemical Oligosaccharide Synthesis: Novel Approach to Traditional Challenges. Automated synthesis of polysaccharides Rational saccharide extension by using the natural product glycosyltransferase LanGT4. New approaches to the chemical synthesis of bioactive oligosaccharides Automated Glycan Assembly: A Perspective A highly efficient synthetic strategy for polymeric support synthesis of Le(x), Le(y), and H-type 2 oligosaccharides Stereocontrolled synthesis of mannans and rhamnans Cross metathesis assisted solid-phase synthesis of glycopeptoids Polymer-supported and chemoenzymatic synthesis of the Neisseria meningitidis pentasaccharide: a methodological comparison Anomeric O-Functionalization of Carbohydrates for Chemical Conjugation to Vaccine Constructs
is cites work of	wds:Q64946906-226D7459-FD0B-4578-9B50-D801BE3FCA16 wds:Q75259489-44A5FFDA-CBD4-41D4-9A79-6E7BA29F2960 wds:Q44217555-3D30D3D8-E1F1-45F9-89DE-C3762E697806 wds:Q37510066-0FADDBA4-0F0A-4621-8A46-C39BEDAEC783 wds:Q92476925-5BD890B6-A595-49FC-94E3-2EDF5AF83281 wds:Q35627032-88A41820-DCA3-4310-B773-AA35DBEF4489 wds:Q44784419-2D0D3DC0-DB7D-4F47-AC80-1BB1FB841FB4 wds:Q33925794-ECFDBF46-651E-47A3-89F6-0CC8F518F9DB wds:Q38361586-06B96C2F-0E1D-4835-8019-830012677808 wds:Q43669118-E8EFE88C-DE74-46F3-92B2-488C042466BB wds:Q84323548-8DD230E1-0210-4405-8F98-320AA4C0239F wds:Q36802338-50F2B3B4-FD5F-4883-84C7-08A9D494EA1A wds:Q90293519-12303572-2248-41C1-A047-A485F003684C wds:Q34489520-2AE4E074-B948-4EFE-A8A5-2EC9F18711C7 wds:Q61455356-52AC6EE7-A37A-4F4E-88EE-F21C6FE31C5F

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