About: Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox")

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About: Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique (publié 2007) (fr) наукова стаття, опублікована в січні 2007 (uk) artículu científicu espublizáu en xineru de 2007 (ast) artikull shkencor i botuar më 01 janar 2007 (sq) scientific article published on 01 January 2007 (en)
publication date	wds:Q80383037-732FA8C1-4485-4F07-AC5E-4FF827C82FF4
publication date	2007-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q80383037-4CE424FD-7A39-4ACB-9AB5-725CA5D4F494 wds:Q80383037-6C99D96E-2967-46EC-9237-98996A50A66A wds:Q80383037-A94E392D-5736-4DAD-8DD1-935429227326
author name string	Lutz H Gade Stéphane Bellemin-Laponnaz Carole Foltz
rdfs:label	Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (en) Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (nl) Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (sq)
skos:prefLabel	Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (en) Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (nl) Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (sq)
name	Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (en) Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (nl) Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (sq)
author	wds:Q80383037-0C701545-5E64-4523-A62F-8CF6CA77488E wds:Q80383037-2C6846B1-0DCE-41BD-90B1-C22BF371E0FB
author	Hubert Wadepohl Markus Enders
title	wds:Q80383037-2921B2B5-A143-4121-B1B3-B287C87DB953
title	Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox") (en)
page(s)	wds:Q80383037-B5F2D378-CD3D-42AA-9737-5ECA59DDB9C7
page(s)	5994-6008
instance of	wds:Q80383037-DCE4CC2C-13B2-43DD-8CA3-C5D85D0BAF57
instance of	scholarly article
main subject	wds:Q80383037-E8996E17-09B0-4CAA-A2A6-48D5494A8A7A
main subject	chirality
PubMed ID	wds:Q80383037-E1E2BB68-F1C6-4740-ABBF-E94E9E85EBE0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17525923
PubMed ID	17525923
published in	wds:Q80383037-38375367-A418-4551-8D7B-412BB80D185A
published in	Chemistry—A European Journal
issue	wds:Q80383037-E6EFA9CD-DF55-4BAB-83C8-CF5233E7476D
volume	wds:Q80383037-38F46FE1-A99C-4265-BFB7-540FE74A74F4
issue	21
volume	13
DOI	wds:Q80383037-8A97A780-D524-467F-AF93-D1FA9AEE33BD
DOI	http://dx.doi.org/10.1002/CHEM.200700307
DOI	10.1002/CHEM.200700307
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80383037
is cites work of	One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles Concise methods for the synthesis of chiral polyoxazolines and their application in asymmetric hydrosilylation Bis(oxazolinylmethyl) Derivatives of C4H4E Heterocycles (E = NH, O, S) asC2-Chiral Meridionally Coordinating Ligands for Nickel and Chromium
is cites work of	wds:Q36558473-FF3FFDD2-B078-47E3-A344-9293412BC40A wds:Q33867988-888817A8-8E23-40BD-8EA1-5D9A58A591F8 wds:Q63982480-3B821C62-F7DB-48A2-8D14-4CA1A6E0F50B

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