About: Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts

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scientific article published on 25 November 2013

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 2013 (uk) article scientifique publié en 2013 (fr) scientific article published on 25 November 2013 (en) artículu científicu espublizáu en payares de 2013 (ast)
publication date	wds:Q86808311-9C61D87C-B870-4D7B-BF43-AA7B466E5B17
publication date	2013-11-25 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q86808311-4E2F187B-8A32-4C59-B701-38051AB69301
language of work or name	English
author name string	wds:Q86808311-3B843D1D-1414-4C36-A149-1ACD47378314 wds:Q86808311-97CE55B2-D343-44D0-97B4-A3E4BB756473 wds:Q86808311-BE27A969-CFE2-4066-9024-C01A61B5B863 wds:Q86808311-C05283CD-808E-4919-BE3A-6E9FE3A40166 wds:Q86808311-F8E62532-1C08-4486-A93A-9C6715BE8234
author name string	Manuel Pérez Douglas W Stephan Roman Dobrovetsky Christopher B Caputo Lindsay J Hounjet
rdfs:label	Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts (en) Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts (nl)
skos:prefLabel	Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts (en) Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts (nl)
name	Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts (en) Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts (nl)
title	wds:Q86808311-62D51175-48AD-4106-B564-CA96CB937FB1
title	Olefin isomerization and hydrosilylation catalysis by Lewis acidic organofluorophosphonium salts (en)
page(s)	wds:Q86808311-5756EFA2-C8B4-4912-8516-6A6B21C5D2A7
page(s)	18308-18310
instance of	wds:Q86808311-D6014CD8-677C-402B-95A5-EFD5F885E035
instance of	scholarly article
PubMed ID	wds:Q86808311-6E4B3D45-3C1D-4A4E-AC46-A1CDE53D9530
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24256456
PubMed ID	24256456
published in	wds:Q86808311-88D45E30-2315-4A78-AB84-454551371AEA
published in	Journal of the American Chemical Society
issue	wds:Q86808311-1D8C70AE-B69F-436D-A8A8-B972B42424C7
volume	wds:Q86808311-83EAAFAD-7587-4577-AB9F-BB5E82D9C268
issue	49
volume	135
DOI	wds:Q86808311-ABF50EB8-FC95-4599-87FD-9A7E67B6C32A
DOI	http://dx.doi.org/10.1021/JA410379X
DOI	10.1021/JA410379X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q86808311
is cites work of	Biphilic Organophosphorus Catalysis: Regioselective Reductive Transposition of Allylic Bromides via P(III)/P(V) Redox Cycling Metal-free transfer hydrogenation of olefins via dehydrocoupling catalysis Intramolecular Diels-Alder reactions of cycloalkenones: stereoselectivity, Lewis acid acceleration, and halogen substituent effects Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines Magnesium hydride alkene insertion and catalytic hydrosilylation Highly selective catalytic -hydroboration of alkynes mediated by borenium cations and B(CF) Carbodiphosphorane mediated synthesis of a triflyloxyphosphonium dication and its reactivity towards nucleophiles. Phosphine and carbene azido-cations: [(L)N3]+ and [(L)2N3]. Fifty Years of Hydrosilylation in Polymer Science: A Review of Current Trends of Low-Cost Transition-Metal and Metal-Free Catalysts, Non-Thermally Triggered Hydrosilylation Reactions, and Industrial Applications Establishing the Role of Triflate Anions in H2 Activation by a Cationic Triorganotin(IV) Lewis Acid
is cites work of	wds:Q38660196-252B2378-B7FD-468B-B7C0-4929CC98944E wds:Q59576327-93251041-A0FE-433B-80F5-C0473DC276A3 wds:Q91791816-E9C39800-845D-4B80-A74F-069739597264 wds:Q34002474-9074D3D0-FD84-4FAA-8201-77E0E45E5081 wds:Q37662412-E271E836-A514-48EA-95AA-A9D23953D0FD wds:Q42263671-4E4B2D10-034A-43C4-8229-CB06359676D0 wds:Q63972301-2B8ED9A6-6217-4EBA-83B8-5B0A9468E47A wds:Q40967834-A03B5B91-5642-4789-8C28-6D0635124F87 wds:Q99241176-0B687524-EDD7-4839-8270-37BFFBB0E1B1 wds:Q64890121-063FC288-69E8-4BE7-8E29-B1117D10E4E4

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