Suzuki-Miyaura coupling in the presence of (2,2,2-triferrocenylethyl) diphenylphosphane

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OriginalspracheEnglisch
Seiten (von - bis)357-360
Seitenumfang4
FachzeitschriftJournal of Organometallic Chemistry
Jahrgang693
Ausgabenummer2
PublikationsstatusVeröffentlicht - 15 Jan. 2008

Abstract

The electron rich and sterically bulky title phosphane was prepared and efficiently applied in the palladium catalyzed Suzuki-Miyaura cross-coupling reaction. With electron rich aryl chlorides and bromides the yields and reaction times were significantly improved by microwave heating.

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Suzuki-Miyaura coupling in the presence of (2,2,2-triferrocenylethyl) diphenylphosphane. / Garabatos-Perera, Jose Ramon; Butenschön, Holger.
in: Journal of Organometallic Chemistry, Jahrgang 693, Nr. 2, 15.01.2008, S. 357-360.

Publikation: Beitrag in FachzeitschriftSurvey PaperForschungPeer-Review

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abstract = "The electron rich and sterically bulky title phosphane was prepared and efficiently applied in the palladium catalyzed Suzuki-Miyaura cross-coupling reaction. With electron rich aryl chlorides and bromides the yields and reaction times were significantly improved by microwave heating.",
keywords = "Cross-coupling, Ferrocene ligands, Palladium, Phosphanes, Suzuki-Miyaura coupling, Triferrocenylmethane",
author = "Garabatos-Perera, {Jose Ramon} and Holger Butensch{\"o}n",
note = "Funding information: This work was kindly supported by the Deutsche Forschungsgemeinschaft. We thank Octel Deutschland GmbH for a donation of ferrocene.",
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TY - JOUR

T1 - Suzuki-Miyaura coupling in the presence of (2,2,2-triferrocenylethyl) diphenylphosphane

AU - Garabatos-Perera, Jose Ramon

AU - Butenschön, Holger

N1 - Funding information: This work was kindly supported by the Deutsche Forschungsgemeinschaft. We thank Octel Deutschland GmbH for a donation of ferrocene.

PY - 2008/1/15

Y1 - 2008/1/15

N2 - The electron rich and sterically bulky title phosphane was prepared and efficiently applied in the palladium catalyzed Suzuki-Miyaura cross-coupling reaction. With electron rich aryl chlorides and bromides the yields and reaction times were significantly improved by microwave heating.

AB - The electron rich and sterically bulky title phosphane was prepared and efficiently applied in the palladium catalyzed Suzuki-Miyaura cross-coupling reaction. With electron rich aryl chlorides and bromides the yields and reaction times were significantly improved by microwave heating.

KW - Cross-coupling

KW - Ferrocene ligands

KW - Palladium

KW - Phosphanes

KW - Suzuki-Miyaura coupling

KW - Triferrocenylmethane

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U2 - 10.1016/j.jorganchem.2007.10.053

DO - 10.1016/j.jorganchem.2007.10.053

M3 - Survey paper

AN - SCOPUS:37348999716

VL - 693

SP - 357

EP - 360

JO - Journal of Organometallic Chemistry

JF - Journal of Organometallic Chemistry

SN - 0022-328X

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