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FLP reactivity of [Ph3C]+ and (o-tolyl)3P and the capture of a Staudinger reaction intermediate

Abstract

The frustrated Lewis pair (FLP) derived from trityl cation and (o-tolyl)3P effects activation of 1,4-cyclohexadiene and RC6H4CCH (R = Br, Me) and heterolytically cleaves the S–S bond of diphenyl disulfide. The FLP also captures pentafluorophenyl azide as the Staudinger reaction intermediate; a species that reacts with Ph3SiH to give the silyl analog.

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Publication details

The article was accepted on 12 May 2017 and first published on 12 May 2017


Article type: Communication
DOI: 10.1039/C7DT01726J
Citation: Dalton Trans., 2017, Accepted Manuscript
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    FLP reactivity of [Ph3C]+ and (o-tolyl)3P and the capture of a Staudinger reaction intermediate

    J. Zhou, L. (. Liu, L. Cao and D. W. Stephan, Dalton Trans., 2017, Accepted Manuscript , DOI: 10.1039/C7DT01726J

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