About: Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes

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About: Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes Goto Sponge NotDistinct Permalink

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scientific article published on 01 February 1999

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1999 (uk) article scientifique publié en 1999 (fr) im Februar 1999 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 1999 (ast) artikull shkencor i botuar më 01 shkurt 1999 (sq) scientific article published on 01 February 1999 (en)
publication date	wds:Q88521505-E2847335-9B2B-47E3-8D0F-3020FAAE9359
publication date	1999-02-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q88521505-1020458B-6DD3-4E57-A037-62CECECDD131 wds:Q88521505-35853DFB-F36F-46B1-BEE4-CA2290531806 wds:Q88521505-866E9F0F-01DA-4D0B-8E19-7CB39125FC55
author name string	Koichi Mikami Kuiling Ding Akihiro Ishii
rdfs:label	Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (en) Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (nl) Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (sq)
skos:prefLabel	Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (en) Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (nl) Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (sq)
name	Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (en) Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (nl) Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (sq)
title	wds:Q88521505-9F39FA1E-83AC-420C-9C02-4524683B8505
title	Super High Throughput Screening (SHTS) of Chiral Ligands and Activators: Asymmetric Activation of Chiral Diol-Zinc Catalysts by Chiral Nitrogen Activators for the Enantioselective Addition of Diethylzinc to Aldehydes (en)
page(s)	wds:Q88521505-EE9999CA-09E6-417A-B163-B51A86438B6F
page(s)	497-501
instance of	wds:Q88521505-163A8DD6-1878-4BAC-9493-AEB6D6E6C1C3
instance of	scholarly article
main subject	wds:Q88521505-35C73A8D-A143-45A1-ADC2-9FCA34EB3107 wds:Q88521505-72DEBBD9-5B64-4ED5-90F9-4DA04A64C784
main subject	chirality enantioselectivity
PubMed ID	wds:Q88521505-85379024-BEFB-4EC4-B3FF-57DBDD79FC47
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/29711785
PubMed ID	29711785
published in	wds:Q88521505-73F93497-D898-48A7-B994-1C0AEAB2F08D
published in	Angewandte Chemie International Edition
issue	wds:Q88521505-B91043DB-CE59-45AA-9697-E09227C71C6F
volume	wds:Q88521505-BCB2837C-5DB4-4E9C-AE78-372268617EBE
issue	4
volume	38
DOI	wds:Q88521505-CDDF70DC-8375-4C68-A17B-E0827B7714A1
DOI	http://dx.doi.org/10.1002/(SICI)1521-3773(19990215)38:4%3C497::AID-ANIE497%3E3.0.CO;2-G
DOI	10.1002/(SICI)1521-3773(19990215)38:4<497::AID-ANIE497>3.0.CO;2-G
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q88521505
is cites work of	Emerging methods for the rapid determination of enantiomeric excess Separation of enantiomers: needs, challenges, perspectives. Directed evolution of enantioselective enzymes for organic chemistry An on-column derivatization method for the determination of the enantiomeric excess of chiral primary amines via indirect enantioseparation by micellar electrokinetic chromatography High-throughput methods for the development of new catalytic asymmetric reactions High-throughput analytical techniques for reaction optimization Using a Lipase as a High-Throughput Screening Method for Measuring the Enantiomeric Excess of Allylic Acetates Engineering Catalysts for Enantioselective Addition of Diethylzinc to Aldehydes with Racemic Amino Alcohols: Nonlinear Effects in Asymmetric Deactivation of Racemic Catalysts Financial support from the National Natural Science Foundation of China, t Chiral N-Acylethylenediamines as New Modular Ligands for the Catalytic Asymmetric Addition of Alkylzinc Reagents to Aldehydes Simultaneous microbatch screening of enantiorecognition on solid chiral selectors using selected mixtures of test-racemates: a case study on cellulose tris(alpha-phenylpropionate) with configurational diversity Development of small focused libraries of supported amino alcohols as an efficient strategy for the optimization of enantioselective heterogeneous catalysts for the ZnEt2 addition to benzaldehyde Fluorous "racemic" mixture synthesis: polysaccharide-based chiral columns for simultaneous demix and enantioseparation of racemic fluorous tagged compounds Chiral H NMR of Atropisomeric Quinazolinones With Enantiopure Phosphoric Acids
is cites work of	wds:Q42162851-5E76E0C4-C9A7-4399-B85C-08A29B2D222B wds:Q73444478-B2BE501F-2BA0-4C5D-AE95-AB4E91108E1B wds:Q34493278-61B5EB86-E8CC-46A8-A1AD-FE59B68355C1 wds:Q34733174-86C023CD-FBBE-43D0-BBE8-417DFB7FFEA3 wds:Q34160381-02EB02E5-D44A-455C-B98D-F83B685336F8 wds:Q31008979-B829B5C4-0FD7-4216-8116-0CA80E7DBD5C wds:Q30674686-C95891DD-846C-4174-985F-97493B211705 wds:Q63209813-FB458223-9D2C-42ED-835F-80E791F76718 wds:Q35053178-6A93C27A-12AE-4BF2-AA9D-0A063FDBE66A wds:Q46801181-A509AE75-DA4D-46F2-AA7E-629AD399BAEE wds:Q58769553-47D80F5E-BB44-40A2-A0FF-D9364F3BE709 wds:Q40777962-569C56A1-A2BE-4A87-956F-02364AC723ED wds:Q44596749-DE9298C2-981D-4691-B896-87E596286F0F

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