About: Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences

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About: Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences Goto Sponge NotDistinct Permalink

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scientific article published on 01 May 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2000 (uk) article scientifique publié en 2000 (fr) im Mai 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en mayu de 2000 (ast) scientific article published on 01 May 2000 (en)
publication date	wds:Q73853303-E1C53DB5-F2DF-4F03-9959-CF07D8F3AEA4
publication date	2000-05-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73853303-FD1E5828-9A9B-47AE-99BA-4A6FFB1E888F
author name string	Breit B
rdfs:label	Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences (en) Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences (nl)
skos:prefLabel	Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences (en) Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences (nl)
name	Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences (en) Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences (nl)
title	wds:Q73853303-96CE58D7-A795-432E-B031-F93927F1A8CD
title	Controlling stereoselectivity with the aid of a reagent-directing group: hydroformylation, cuprate addition, and domino reaction sequences (en)
page(s)	wds:Q73853303-C650836F-22CC-4F22-8414-1ECC2758A9DC
page(s)	1519-1524
instance of	wds:Q73853303-BB0215D4-1201-4B2E-AD4E-6049B49553F8
instance of	scholarly article
main subject	wds:Q73853303-E5C7E643-B4D2-46D9-BE0A-F71045338366
main subject	stereoselectivity
PubMed ID	wds:Q73853303-CDE45F83-486D-444C-9ED0-24EAFB22F802
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10839167
PubMed ID	10839167
published in	wds:Q73853303-45C490F5-7087-4060-A39B-AD31EB7A99AC
published in	Chemistry—A European Journal
issue	wds:Q73853303-75C09B7E-63A7-4541-B4ED-C6F0D38B8B54
volume	wds:Q73853303-39718BDA-A041-45EE-A796-3927067688F9
issue	9
volume	6
DOI	wds:Q73853303-E4317EDB-88FE-492A-B715-FAC3F5E094BC
DOI	http://dx.doi.org/10.1002/(SICI)1521-3765(20000502)6:9%3C1519::AID-CHEM1519%3E3.3.CO;2-Y
DOI	10.1002/(SICI)1521-3765(20000502)6:9<1519::AID-CHEM1519>3.3.CO;2-Y
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73853303
is cites work of	Phosphabenzenes as monodentate pi-acceptor ligands for rhodium-catalyzed hydroformylation Metallacycle-Mediated Cross-Coupling with Substituted and Electronically Unactivated Alkenes Neighbouring-Group Effects in Heck Reactions α-Lithiated (R,R)-TMCDA as an Efficient Building Block for the Preparation of Chiral N,N,O Ligands by Asymmetric 1,2-Addition The Development of Alkoxide-Directed Metallacycle-Mediated Annulative Cross-Coupling Chemistry A Transient-Directing-Group Strategy Enables Enantioselective Reductive Heck Hydroarylation of Alkenes
is cites work of	wds:Q38464492-00B535D7-DFF4-4B46-8404-0BAA9A26479F wds:Q59203581-9CADD4D1-0EE2-49E2-B418-EF9BB8B3C13B wds:Q62705645-CDC92251-C86C-47AF-B1D0-2E0C20F53852 wds:Q39399650-7E1358CD-F255-4805-A6DF-7D430A551B7B wds:Q43701308-A8419969-ACE0-4D2D-ABF5-98D31C724098 wds:Q90512374-56244758-181E-4E6B-B280-9A52F23C2A4F

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