About: [(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère

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About: [(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2001 (uk) مقالة علمية تنشرت ف 1 دجنبر 2001 (ary) article scientifique publié en 2001 (fr) im Dezember 2001 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q95391967-3C8CEECC-7412-4BC2-A3B9-A0B7B1BC3924
publication date	2001-12-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q95391967-09F53526-B191-4B25-B2DA-5665F3B12A78 wds:Q95391967-46A9B944-2443-4D63-B142-285FE5DB87E4 wds:Q95391967-5ACE93B3-42A3-4193-950F-3D77E666E91C wds:Q95391967-A83D53EF-F920-4015-B04E-E79C8839B8A4 wds:Q95391967-D6BD0755-C3E2-4E5F-A862-40B6AD1130A5
author name string	Gérald Bernardinelli Valérie Alezra Florian Viton Christophe M. Saudan E. Peter Kündig
rdfs:label	[(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère (en) [(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère (nl)
skos:prefLabel	[(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère (en) [(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère (nl)
name	[(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère (en) [(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère (nl)
title	wds:Q95391967-3819F7A4-4621-4842-B968-1C9393609E93
title	[(Indenyl)Ru(biphop-F)](+): A Lewis Acid Catalyst That Controls both the Diene and the Dienophile Facial Selectivity in Diels-Alder Reactions This work was supported by the Swiss National Science Foundation (FNS grant 20-59374.99) and The Ministère des Affaires Etrangères from France (Lavoisier grant to V.A.). biphop-F=1,2-bis[bis(pentafluorophenyl)phosphanyloxy]-1,2-diphenylethane (en)
page(s)	wds:Q95391967-44CE4667-DCE3-466F-9917-EE5FBB8B9637
page(s)	4481-4485
instance of	wds:Q95391967-FDA36C23-B49A-435F-98BD-086A689AA843
instance of	scholarly article
PubMed ID	wds:Q95391967-AC943E4A-422B-4188-8572-630B04D4AFF8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12404453
PubMed ID	12404453
published in	wds:Q95391967-0F332D5B-B437-48F6-AB56-FF202BD3E23F
published in	Angewandte Chemie International Edition
issue	wds:Q95391967-2DB0E630-9F40-4D38-9C09-403B7A980F38
volume	wds:Q95391967-1968F9C1-4A50-4909-BF3D-93FD9511189D
issue	23
volume	40
DOI	wds:Q95391967-19755357-7DB8-402B-8BAB-7E8DD541A5CB
DOI	http://dx.doi.org/10.1002/1521-3773(20011203)40:23%3C4481::AID-ANIE4481%3E3.0.CO;2-A
DOI	10.1002/1521-3773(20011203)40:23<4481::AID-ANIE4481>3.0.CO;2-A
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q95391967
is cites work of	Arene-ruthenium complexes with salicyloxazolines: diastereoselective synthesis, configurational stability and applications as asymmetric catalysts for Diels-Alder reactions Chiral Half-Sandwich Ruthenium(II) Complexes as Catalysts in 1,3-Dipolar Cycloaddition Reactions of Nitrones with Methacrolein Indenylmetal Catalysis in Organic Synthesis
is cites work of	wds:Q59617386-56186129-3C28-40D2-B109-5CB3E4A18BB3 wds:Q38996893-38D6D4BB-7025-4B77-85EF-D490E7C5AC2C wds:Q44977620-8AA14A78-01CE-4C94-8B47-705A36C47365

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