About: Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide

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About: Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide Goto Sponge NotDistinct Permalink

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scientific article published on 01 April 1990

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1990 (uk) im April 1990 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 1990 (ast) scientific article published on 01 April 1990 (en)
publication date	wds:Q68872677-6985D501-83FB-4D61-81B3-639012583D2A
publication date	1990-04-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q68872677-0904E043-0EA0-4778-AE49-B3C4D2DD2B08 wds:Q68872677-18018959-C400-494A-AF9B-4DC380EF5431 wds:Q68872677-3BCF4608-BD5F-4956-B2C7-A7A6544EFC05 wds:Q68872677-4D43552F-4B1C-4822-8F04-9BBE6E422FB1
author name string	H Ishida A Hasegawa M Kiso A Kameyama
rdfs:label	Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide (en) Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide (nl)
skos:prefLabel	Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide (en) Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide (nl)
name	Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide (en) Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide (nl)
title	wds:Q68872677-A38D80C3-158D-432C-81E1-BF3A29351CB2
title	Stereoselective synthesis of sialyl-lactotetraosylceramide and sialylneolactotetraosylceramide (en)
page(s)	wds:Q68872677-7B7519ED-3566-463B-8628-079F5A210F4D
page(s)	269-285
instance of	wds:Q68872677-62504E85-9CF3-4883-86B1-60A429EDFE71
instance of	scholarly article
main subject	wds:Q68872677-2104EA51-A442-4881-B6E5-B9908BBFFF44
main subject	stereoselectivity
PubMed ID	wds:Q68872677-C6632194-A845-4EF8-BFE5-14BEC5DC7849
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2379209
PubMed ID	2379209
published in	wds:Q68872677-CFD970E6-D758-4FDB-BA81-1742417079F1
published in	Carbohydrate Research
volume	wds:Q68872677-63C52027-6DA9-4753-879E-AE10A50E2D94
volume	200
DOI	wds:Q68872677-D00C8CF8-8593-4508-9B15-63C7F187B69C
DOI	http://dx.doi.org/10.1016/0008-6215(90)84197-3
DOI	10.1016/0008-6215(90)84197-3
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q68872677
is cites work of	Substitution of amino acid residue in influenza A virus hemagglutinin affects recognition of sialyl-oligosaccharides containing N-glycolylneuraminic acid Anomeric-oxygen activation for glycoside synthesis: the trichloroacetimidate method Molecular cloning and expression of a sixth type of alpha 2,8-sialyltransferase (ST8Sia VI) that sialylates O-glycans A concise synthesis of the 6-O- and 6'-O-sulfated analogues of the sialyl Lewis X tetrasaccharide Systematic synthesis and MAG-binding activity of novel sulfated GM1b analogues as mimics of Chol-1 (alpha-series) gangliosides: highly active ligands for neural siglecs A novel and versatile glycosyl donor for the preparation of glycosides of N-acetylneuraminic acid Sulphatide binds to human and animal influenza A viruses, and inhibits the viral infection Renewed synthetic approach to gangliosides exploiting versatile and powerful synthetic units. Facile enzymatic conversion of lactose into lacto-N-tetraose and lacto-N-neotetraose The synthesis and biological evaluation of lactose-based sialylmimetics as inhibitors of rotaviral infection Synthesis of Lactose-Based S-Linked Sialylmimetics of α(2,3)-Sialosides Synthesis and biological activity of glycolipids, with a focus on gangliosides and sulfatide analogs Synthesis and biological activities of three sulfated sialyl Le(x) ganglioside analogues for clarifying the real carbohydrate ligand structure of L-selectin Stereocontrolled synthesis of sialyl Lewis X ceramide consisting of a pentasaccharide recognized by the selectin family Total synthesis of sialyl Lewis X Synthesis of sialyl Le(x) ganglioside analogues sulfated at C-6 of either the galactose or N-acetylglucosamine residues, and at both of the galactose and N-acetylglucosamine residues: probes for clarifying the real carbohydrate ligand of L-selectin Study of glycosylation with N-trichloroacetyl-D-glucosamine derivatives in the syntheses of the spacer-armed pentasaccharides sialyl lacto-N-neotetraose and sialyl lacto-N-tetraose, their fragments, and analogues Synthesis of sialyl LeX ganglioside analogues modified at C-6 of the galactose residue to elucidate the mechanism of selection recognition. Synthesis of two analogues of the Sda determinant. Replacement of the sialic acid residue by a sulfate or a carboxymethyl group Synthetic studies on glycosphingolipids from the parasite Echinococcus multilocularis Systematic synthesis of N-methyl-1-deoxynojirimycin-containing, Le(x), Le(a), sialyl-Le(x) and sialyl-Le(a) epitopes recognized by selectins Cloning and Overexpression of β-N-Acetylglucosaminidase Encoding GenenagAfromAspergillus oryzaeand Enzyme-catalyzed Synthesis of Human Milk Oligosaccharide The chemistry of oligosaccharide ligands of selectins: significance for the development of new immunomodulatory medicines Total synthesis of a cholinergic neuron-specific ganglioside GT1a alpha: a high affinity ligand for myelin-associated glycoprotein (MAG). Synthesis of disialoganglioside GD1 alpha and its positional isomer First total synthesis of ganglioside GT1a alpha A facile total synthesis of ganglioside GM1b and its positional analog Enzymic synthesis of lacto-N-triose II and its positional analogues A synthetic approach to the c-series gangliosides containing sialyl-alpha(2-->8)sialyl-alpha(2-->8)sialic acid: synthesis of ganglioside GT4, alpha(2-->6) GT4 and GT3 Synthesis of a spacer-armed disulfated tetrasaccharide of SB1a, a carbohydrate hapten associated with human hepatocellular carcinoma Synthesis of cerebroside, lactosyl ceramide, and ganglioside GM3 analogs containing beta-thioglycosidically linked ceramide A first total synthesis of a novel sulfated ganglioside, 3'-O-sulfo-GM1b Polymer-supported and chemoenzymatic synthesis of the Neisseria meningitidis pentasaccharide: a methodological comparison Synthesis and selectin-binding activity of N-deacetylsialyl Lewis X ganglioside Novel sulfated gangliosides, high-affinity ligands for neural siglecs, inhibit NADase activity of leukocyte cell surface antigen CD38. Roles of GalNAc-disialyl Lactotetraosyl Antigens in Renal Cancer Cells.
is cites work of	wds:Q38320121-9A29F7FE-7555-4EE9-A7A5-CDECFBC71571 wds:Q73019576-56EEDF5C-4D9C-4836-AE92-3B43A7E79F31 wds:Q38308632-A060E2C3-1757-40F5-859F-98A2E2ACFCCD wds:Q41911352-80B31EAC-B1A3-482E-A3D6-86775AC867E9 wds:Q73457091-24B46A77-7933-40EB-AA8C-3CD0F4F7031E wds:Q74068600-CC1BF3CE-1885-4312-8079-63FD52C6611D wds:Q38317034-6FA2AC05-08BF-4A6B-8300-7A7675C26470 wds:Q44424510-AA5C3B1B-E37F-412B-96B0-461A97D3A140 wds:Q67589360-46F27BE2-19CD-46DC-9384-73D419FF738B wds:Q41172064-C2DBABF2-25C3-4E27-9700-4F4E0DB90338 wds:Q45723778-B26266CE-1A83-49EA-AA4D-121BC882F6E3 wds:Q57242604-8BD67DAB-0F08-4440-AA7B-367C2A2106BB wds:Q73186793-F595076B-21CA-4045-A10E-C785D4904340 wds:Q24295378-052E6C26-3826-49C4-A67C-CC82F4D3D802 wds:Q43721756-EFE900D3-BD49-4BA2-AAEE-F20D053FDB7B wds:Q44217560-68A917F2-AC10-43A9-8AFC-59FF0E3E9BEC wds:Q78042033-42BAD87D-E894-43B3-99CF-674D7D23FBD1 wds:Q72759073-0108CF6A-7D20-4209-B644-199952936894 wds:Q34523324-45B06378-6878-4B14-87FE-CCECDAFA13B5 wds:Q44210945-9B0C3771-B1F9-457D-B2F8-282A3C9437DE wds:Q46721473-632AC4E5-6C63-47F0-AA24-C9318F03301D wds:Q73367842-6AFDAA36-8E8A-4ED2-BDF4-2FF27686EDDF wds:Q44217605-E688427C-E735-47A2-8164-93767892B6A3

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