About: Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls

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About: Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 2002

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2002 (uk) مقالة علمية تنشرت ف 1 أكتوبر 2002 (ary) im Oktober 2002 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 2002 (ast) scientific article published on 01 October 2002 (en)
publication date	wds:Q78361790-BD87C72E-CD6D-499C-9F8F-53F4FF32AB28
publication date	2002-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q78361790-689B234E-AD5D-4626-A52E-84FBDF3E5973 wds:Q78361790-A9CCCB61-1B0D-40DC-955A-DB06BC520F75 wds:Q78361790-D3FB736B-7297-45D0-AE98-470BED9AD4A8
author name string	Kyoung Hoon Kim Dong-Hyun Ko Deok-Chan Ha
rdfs:label	Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls (en) Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls (nl)
skos:prefLabel	Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls (en) Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls (nl)
name	Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls (en) Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls (nl)
title	wds:Q78361790-34E1422E-2C8F-458C-A6F3-798231AFCCAE
title	Enantioselective additions of diethylzinc and diphenylzinc to aldehydes using 2-dialkyl-aminomethyl-2'-hydroxy- 1,1'-binaphthyls (en)
page(s)	wds:Q78361790-D3F90A10-F5EF-4201-A127-3F5AAAE8BB1D
page(s)	3759-3762
instance of	wds:Q78361790-D4BEDF40-919D-47C1-85D1-80EC38B32172
instance of	scholarly article
main subject	wds:Q78361790-FB13C6EB-9301-4BA0-8A71-F4D2141A5B61
main subject	enantioselectivity
PubMed ID	wds:Q78361790-E3F3106A-C407-4E60-8B23-00B1D60E732F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12375937
PubMed ID	12375937
published in	wds:Q78361790-FFD826CE-B883-46F7-8110-6EC2C3DC5690
published in	Organic Letters
issue	wds:Q78361790-C81FF102-7CAB-46E8-AAD0-BF0627196049
volume	wds:Q78361790-5993FEF0-CDF6-4E2C-A0D5-922CF27023A8
issue	21
volume	4
DOI	wds:Q78361790-E73C39BB-685F-4472-A51B-A08370C3C60E
DOI	http://dx.doi.org/10.1021/OL026761J
DOI	10.1021/OL026761J
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q78361790
is cites work of	Structural influence of chiral tertiary aminonaphthol ligands on the asymmetric phenyl transfer to aromatic aldehydes Continuous flow enantioselective arylation of aldehydes with ArZnEt using triarylboroxins as the ultimate source of aryl groups Practical catalytic asymmetric synthesis of diaryl-, aryl heteroaryl-, and diheteroarylmethanols Catalytic asymmetric addition of diphenylzinc to cyclic alpha,beta-unsaturated ketones. Mannich andO-Alkylation Reactions of Tetraalkoxyresorcin[4]arenes – The Use of Some Products in Ligand-Assisted Reactions 1,3-Bis[N-sulfonyl-(1R,2S)-1,3-diphenyl-2-aminopropanol]benzene: an excellent ligand for titanium-catalyzed asymmetric AlPh3(THF) additions to aldehydes New atropisomeric amino alcohol ligands for enantioselective addition of diethylzinc to aldehydes
is cites work of	wds:Q85113488-366E4F2F-12AC-4159-B767-ABE530928AEC wds:Q41808988-D8BE47D4-B140-4977-8769-BC7650D8222E wds:Q37370256-0E84A0EF-2D4B-438F-8B7B-E01E76511A50 wds:Q60649305-10FDDB45-D060-4995-9784-0C889488C4DA wds:Q37681531-B28B9F97-D9B0-43D6-A80D-9DE451E8FD08 wds:Q86421644-63745064-E7C6-4915-B895-D3BAEFF0C9CA wds:Q46553547-D326669A-AC5C-47AD-846D-0BB70F144C88

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