Issue 10, 2013
From the journal:

Dalton Transactions

Hydrophosphination of vinyl-boranes with phosphinoamines†

Chunfang Jianga  and  Douglas W. Stephan*a  

* Corresponding authors

a Department of Chemistry, University of Toronto, Toronto, Ontario, Canada
E-mail: dstephan@chem.utoronto.ca

Abstract

Phosphinoamine ligands PhN(H)PR2 (R = iPr 1, tBu 2) react with R1CH[double bond, length as m-dash]CR2B(C6F5)2 (R1 = Ph, p-FC6H4, nPr, Et, R2 = H, Ph, Et, C6F5) to effect uncatalyzed hydrophosphination of the olefinic bond, affording the C2BNP five-membered cyclization compounds 3–14. All the compounds are fully characterized and compounds 4, 7, 8 and 9 are studied by X-ray diffraction analysis.

Graphical abstract: Hydrophosphination of vinyl-boranes with phosphinoamines

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Article information

DOI
https://doi.org/10.1039/C2DT32677A
Article type
Paper
Submitted
09 Nov 2012
Accepted
11 Dec 2012
First published
04 Jan 2013

Dalton Trans., 2013,42, 3318-3325

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Hydrophosphination of vinyl-boranes with phosphinoamines

C. Jiang and D. W. Stephan, Dalton Trans., 2013, 42, 3318 DOI: 10.1039/C2DT32677A

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