About: Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC

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About: Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC Goto Sponge NotDistinct Permalink

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scientific article published on 01 September 1996

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 1996 (uk) article scientifique publié en 1996 (fr) im September 1996 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 1996 (ast) scientific article published on 01 September 1996 (en)
publication date	wds:Q71507027-D95CE9AB-1FFF-426D-9A8D-77D88E5294E8
publication date	1996-09-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q71507027-ACCBFD16-A4FF-4254-9906-157B63026AF2
language of work or name	English
author name string	wds:Q71507027-0C9FF8D1-57A3-41C6-B411-D25B32D0512F wds:Q71507027-31EF8F62-E716-4560-BC80-5B58D44E7D2F wds:Q71507027-4E3FA716-ABF8-4517-8764-916AC7451040 wds:Q71507027-675AD006-2BA2-4CB4-AAFC-35424780ABB5 wds:Q71507027-EBFA4CD6-816F-48C4-8B23-D70499052E3A wds:Q71507027-ECF71F79-CCC4-4FE1-A454-9BB98FF767A9 wds:Q71507027-FF6A2B7B-FDE4-4955-AC9D-EEE206168338
author name string	Y Kawamura N Enomoto Y Ogasawara S Furukawa Y Okamoto E Yashima H Akano
rdfs:label	Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC (en) Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC (nl)
skos:prefLabel	Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC (en) Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC (nl)
name	Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC (en) Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC (nl)
title	wds:Q71507027-C6A665C9-2A64-44C6-A661-F0034AF44744
title	Preparation of silica gel-bonded amylose through enzyme-catalyzed polymerization and chiral recognition ability of its phenylcarbamate derivative in HPLC (en)
page(s)	wds:Q71507027-69FCFD6C-70F0-476E-A466-490791DE3999
page(s)	2798-2804
instance of	wds:Q71507027-AD01A733-C68C-4766-BAB1-7624653F8063
instance of	scholarly article
main subject	wds:Q71507027-F89FAF03-6000-45A9-A5BF-827C49CB6BF4
main subject	chirality
PubMed ID	wds:Q71507027-06FFA459-FD5B-414C-9B49-2115A007609A
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8794916
PubMed ID	8794916
published in	wds:Q71507027-C6B9C8A2-271A-404A-AF61-5EE623410CFD
published in	Analytical Chemistry
issue	wds:Q71507027-62E24814-EA5E-4E96-8F72-0337D5B97692
volume	wds:Q71507027-E9C543A6-9461-4886-BB42-2300E6DB7CED
issue	17
volume	68
DOI	wds:Q71507027-66D4F9A0-AA64-421B-9FAF-03F3B57860E9
DOI	http://dx.doi.org/10.1021/AC960002V
DOI	10.1021/AC960002V
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71507027
is cites work of	Chiral beta-cyclodextrin-based polymer supports prepared via ring-opening metathesis graft-polymerization Chiral recognition ability and solvent versatility of bonded amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase: enantioselective liquid chromatographic resolution of racemic N-alkylated barbiturates and thalidomide analogs Chiral separation by chromatographic and electromigration techniques. A review Amylose engineering: phosphorylase-catalyzed polymerization of functional saccharide primers for glycobiomaterials Polysaccharide-based chiral stationary phases for high-performance liquid chromatographic enantioseparation Covalently bonded polysaccharide derivatives as chiral stationary phases in high-performance liquid chromatography Novel Amide-Based Molecular Knots: Complete Enantiomeric Separation, Chiroptical Properties, and Absolute Configuration We would like to thank Prof. F. V. Schurig for his advice regarding the separation of the enantiomers. The results reported here Preparative enantioseparation by simulated moving bed chromatography Preparation of chiral stationary phase for HPLC based on immobilization of cellulose 3,5-dimethylphenylcarbamate derivatives on silica gel. Liquid chromatographic separation of darunavir enantiomers on coated and immobilized amylose tris(3, 5-dimethylphenylcarbamate) chiral stationary phases Enantioseparation using selected polysaccharides as chiral buffer additives in capillary electrophoresis Enantioselectivity of monolithic silica stationary phases immobilized with different concentrations cellulose tris (3,5-dimethylphenylcarbamate), analyzed with different mobile phases in capillary electrochromatography Enantioseparation on Riboflavin Derivatives Chemically Bonded to Silica Gel as Chiral Stationary Phases for HPLC Long Chain-Substituted and Triply Functionalized Molecular Knots – Synthesis, Topological Chirality and Monolayer Formation Immobilization and chiral recognition of 3,5-dimethylphenylcarbamates of cellulose and amylose bearing 4-(trimethoxysilyl)phenylcarbamate groups. Comparative studies between covalently immobilized and coated chiral stationary phases based on polysaccharide derivatives for enantiomer separation of N-protected alpha-amino acids and their ester derivatives
is cites work of	wds:Q32055589-D1E385B2-940C-4946-989D-58774D533D68 wds:Q38922981-CD04BA59-6A14-44A0-9988-63F5458E7283 wds:Q34160349-D0A0C55A-E429-4D1A-B348-31BD2AD6545C wds:Q34522296-6F486D09-DDAD-49CB-B76E-1AF6D4DD02EC wds:Q85066031-3AE722C1-E46A-4979-9DFC-59EC163E4C16 wds:Q44239089-A46DA105-F000-4280-82FF-FE34DE2CDC22 wds:Q60245786-9D2106D4-774F-449D-9684-4D605DD50201 wds:Q62073162-BE902535-A16C-4478-A1F3-88361752BB48 wds:Q84190624-2AB3A166-C64A-4088-9E1B-A6186E0E5932 wds:Q34160339-9835813A-57E8-423D-9018-F3EF3DE76D67 wds:Q46004490-A6D00883-F0A7-49C4-B678-6BBBB589216C wds:Q80061888-F09B6506-3228-4FA3-B6C7-4E7493C28DE4 wds:Q74157309-9D252391-A11D-49C9-A8DE-A0B8A2BD3FA2 wds:Q73522550-1B68963B-AA20-4C06-8803-F3FBBB01BE66 wds:Q46249311-1FA78781-F189-4B27-970C-04B582F9FB36 wds:Q34160410-4D4692AF-02D3-44C0-9D7A-DBC87F5D41DE

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