A Bis(oxazolinyl)pyrrole as a New Monoanionic Tridentate Supporting Ligand: Synthesis of a Highly Active Palladium Catalyst for Suzuki-Type C-C Coupling

Mazet, Clement; Gade, Lutz H.

doi:10.1021/om010586d

Scientific article

English

A Bis(oxazolinyl)pyrrole as a New Monoanionic Tridentate Supporting Ligand: Synthesis of a Highly Active Palladium Catalyst for Suzuki-Type C-C Coupling

ContributorsMazet, Clement; Gade, Lutz H.

Published inOrganometallics, vol. 20, no. 20, p. 4144-4146

Publication date2001

Abstract

Reaction of pyrrole-2,5-biscarbonitrile with 2-amino-2-methyl-1-propanol gave the bis{2-(4,4‘-dimethyl-4,5-dihydrooxazolyl)}pyrrole (dmoxpH) (1), which was deprotonated and reacted with [PdCl2(COD] to give [Pd2(dmoxp)2Cl2] (2) and [Pd3(dmoxp)2Cl4] (3). The former is an active catalyst in the Suzuki cross coupling of phenylboronic acid with activated and nonactivated aryl bromides at 70 °C and catalyst/substrate ratios of 10-4 to 10-5.

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Citation (ISO format)

MAZET, Clement, GADE, Lutz H. A Bis(oxazolinyl)pyrrole as a New Monoanionic Tridentate Supporting Ligand: Synthesis of a Highly Active Palladium Catalyst for Suzuki-Type C-C Coupling. In: Organometallics, 2001, vol. 20, n° 20, p. 4144–4146. doi: 10.1021/om010586d

Article

Identifiers

PID : unige:6940
DOI : 10.1021/om010586d

Journal ISSN0276-7333

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A Bis(oxazolinyl)pyrrole as a New Monoanionic Tridentate Supporting Ligand: Synthesis of a Highly Active Palladium Catalyst for Suzuki-Type C-C Coupling

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