About: Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations

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About: Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2016 (fr) наукова стаття, опублікована в березні 2016 (uk) im März 2016 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q59203334-8F58BD0C-046D-47E7-9860-B9C4EBC28847
publication date	2016-03-29 00:00:00Z (xsd:dateTime)
author name string	wds:Q59203334-0514620D-C0A2-4178-B39C-0F5D772104DE wds:Q59203334-60C8444F-5B18-4DE9-B81F-6FB1E9B2153A wds:Q59203334-67741E03-622B-4A49-8F4E-FAF1524819EF wds:Q59203334-C791F9BF-B4C3-4A4F-BEF8-C06CAE9DDAF8 wds:Q59203334-F43CD3DF-08C4-4C9B-B565-7C19C04D9A88
author name string	Manuel Perez Douglas W. Stephan Digvijay Porwal Meera Mehta Isaac Garcia de la Arada
rdfs:label	Metal-Free Phosphine Oxide Reductions Catalyzed by B (nl) Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations (en)
skos:prefLabel	Metal-Free Phosphine Oxide Reductions Catalyzed by B (nl) Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations (en)
name	Metal-Free Phosphine Oxide Reductions Catalyzed by B (nl) Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations (en)
author	wds:Q59203334-9A08779E-C524-4A9F-8107-FCF51160A14B
author	Martin Oestreich
title	wds:Q59203334-38A56FB8-ECF1-473D-82E9-8ACA7C3E9F23
title	Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations (en)
page(s)	wds:Q59203334-F359E4D9-D8C6-4355-85AC-4C26F6FF4041
page(s)	1030-1035
instance of	wds:Q59203334-A71AD10E-7196-4EF1-B3B2-F65B17551064
instance of	scholarly article
published in	wds:Q59203334-ACB3C822-9540-4335-A0BE-7DAC2BB265D5
published in	Organometallics
issue	wds:Q59203334-A8745707-C06C-4AB8-BF4C-4E66DBF568AF
volume	wds:Q59203334-229CE65E-43E9-45DE-BBC4-72813A508442
issue	7
volume	35
DOI	wds:Q59203334-3A562DAF-F303-4627-A7A5-2A0C8235F4CE
DOI	http://dx.doi.org/10.1021/ACS.ORGANOMET.6B00158
DOI	10.1021/ACS.ORGANOMET.6B00158
Fatcat ID	wds:Q59203334-6D93C353-0D7D-4686-B911-95B9C422CF93
Fatcat ID	release_orejidcnozbjldxpxl3l3kdgqq
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59203334
is cites work of	Poly(methylhydrosiloxane) as a green reducing agent in organophosphorus-catalysed amide bond formation. Electrophilic Activation of Silicon-Hydrogen Bonds in Catalytic Hydrosilations Cooperative Lewis acidity in borane-substituted fluorophosphonium cations. N-Methyl-Benzothiazolium Salts as Carbon Lewis Acids for Si-H σ-Bond Activation and Catalytic (De)hydrosilylation Catalytic reduction of amides to amines by electrophilic phosphonium cations via FLP hydrosilylation. Efficient phosphine-mediated formal C(sp3)-C(sp3) coupling reactions of alkyl halides in batch and flow. A Tale of Two Elements: The Lewis Acidity/Basicity Umpolung of Boron and Phosphorus Metal-free pincer ligand chemistry polycationic phosphonium Lewis acids Air- and water-stable Lewis acids: synthesis and reactivity of P-trifluoromethyl electrophilic phosphonium cations. Catalytic double hydroarylation of alkynes to 9,9-disubstituted 9,10-dihydroacridine derivatives by an electrophilic phenoxyphosphonium dication. B(C6F5)3-Catalyzed Reduction of Aromatic and Aliphatic Nitro Groups with Hydrosilanes A model for C–F activation by electrophilic phosphonium cations Eine Geschichte über zwei Elemente: die Umpolung der Lewis-Acidität/Basizität von Bor und Phosphor Synthesis and oxidation of phosphine cations. A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane.
is cites work of	wds:Q50196457-30ACB4A4-D38A-41F9-83E8-657043236B54 wds:Q53567464-A786A751-DB8E-4D22-A37A-A0EF9A616CBB wds:Q53708379-DE2BC18E-BB98-4E39-A8F6-95F66F60C749 wds:Q46408132-7C2B9DE3-D3DD-4C0F-9528-5BFE7E660BEB wds:Q47731304-96FF27A3-A9FF-4787-A77A-DA0E8B95F0CC wds:Q54045295-56EE27C3-4535-489F-A1BA-A71243805B87 wds:Q59203327-C283D151-6987-4949-9FD7-4D65A287A93D wds:Q39134836-C0320FD3-F284-4F3B-B576-801D8FEDE0C0 wds:Q57394682-656CCCA9-11CB-48CE-9EA3-5FF1E955A11A wds:Q57394684-9E8B6F06-8FEE-4B4A-A484-29C1B7817FD2 wds:Q31138954-EB5B2EE2-D7E8-4FAD-B35C-2A8FE7643FF2 wds:Q46294167-A1F99F44-F0E1-410F-AB3A-E9EED9B99636 wds:Q38957956-653900D7-47EB-4609-8CE5-62543C496097 wds:Q52813389-E2DF5C12-FDB7-4BD9-8974-5F0C09FB11A6 wds:Q50007006-5C5DD8E8-A5CF-4ED9-97A7-64B8D2166250

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