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Hydrophosphonylation of alkenes or nitriles by double radical transfer mediated by titanocene/propylene oxide
Journal article   Peer reviewed

Hydrophosphonylation of alkenes or nitriles by double radical transfer mediated by titanocene/propylene oxide

Camille Midrier, Mathias Lantsoght, Jean-Noël Volle, Jean-Luc Pirat, David Virieux and Christian V. Stevens
Tetrahedron Letters, Vol.52, pp.6693-6696
02/10/2011

Abstract

Radical Titanocene Hydrophosphonylation Alkenes Nitriles
Hydrophosphonylation reactions have emerged as efficient processes for the functionalization of alkenes or alkynes. Synthesis of alkylphosphonates was achieved by an original double radical transfer mediated by titanocene and propylene oxide. By the same way, nitriles which are considered as inert functions in radical process lead to aminobisphosphonates.
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