Direct Synthesis of Amino-substituted Aromatic Phosphonates via Palladium-catalyzed Coupling of Aromatic Mono- and Dibromides with Diethyl Phosphite

Direct Synthesis of Amino-substituted Aromatic Phosphonates via Palladium-catalyzed Coupling of Aromatic Mono- and Dibromides with Diethyl Phosphite

An efficient Pd-catalyzed carbon–phosphorus bond-forming route is described for the direct synthesis of diethyl arylphosphonates bearing amino and alkylamino groups on the aromatic ring.

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Veröffentlicht in:Chemistry letters 2009-07, Vol.38 (7), p.738-739
Hauptverfasser: Bessmertnykh, Alla, Douaihy, Christiane Morkos, Guilard, Roger
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Organic chemistry
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container_issue 7
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container_title Chemistry letters
container_volume 38
creator Bessmertnykh, Alla
Douaihy, Christiane Morkos
Guilard, Roger
description An efficient Pd-catalyzed carbon–phosphorus bond-forming route is described for the direct synthesis of diethyl arylphosphonates bearing amino and alkylamino groups on the aromatic ring.
doi_str_mv 10.1246/cl.2009.738
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source Oxford University Press Journals All Titles (1996-Current)
subjects Chemical Sciences
Organic chemistry
title Direct Synthesis of Amino-substituted Aromatic Phosphonates via Palladium-catalyzed Coupling of Aromatic Mono- and Dibromides with Diethyl Phosphite
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