Issue 5, 2002

Synthesis of the first 1,2,3,4-azatriphospholene complex

Abstract

Synthesis of the first 1,2,3,4-azatriphospholene complex was achieved by heating a solution of a P-phenyl-substituted 7-phosphanorbornadiene tungsten complex and triphenylphosphonio cyanomethylide, whereby CH-insertion products were formed in a competing reaction; these results also provide first evidence for the ability of electrophilic terminal phosphanediyl complexes to react at the ylide carbon atom and at the carbonitrile nitrogen atom of Wittig-ylides having a nitrile functional group; the structures of both complexes were established through X-ray single-crystal diffraction studies.

Graphical abstract: Synthesis of the first 1,2,3,4-azatriphospholene complex

Supplementary files

Article information

Article type
Communication
Submitted
26 Nov 2001
Accepted
17 Jan 2002
First published
04 Feb 2002

Chem. Commun., 2002, 454-455

Synthesis of the first 1,2,3,4-azatriphospholene complex

N. Hoffmann, C. Wismach, P. G. Jones, R. Streubel, N. H. T. Huy and F. Mathey, Chem. Commun., 2002, 454 DOI: 10.1039/B110803B

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