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

Jose Ramon Garabatos-Perera; Holger Butenschön

doi:10.1016/j.jorganchem.2007.10.053

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

Jose Ramon Garabatos-Perera
, Holger Butenschön^*

^*Korrespondierende*r Autor*in für diese Arbeit

Institut für Organische Chemie

Publikation: Beitrag in Fachzeitschrift › Survey Paper › Forschung › Peer-Review

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.

Originalsprache	Englisch
Seiten (von - bis)	357-360
Seitenumfang	4
Fachzeitschrift	Journal of Organometallic Chemistry
Jahrgang	693
Ausgabenummer	2
DOIs	https://doi.org/10.1016/j.jorganchem.2007.10.053
Publikationsstatus	Veröffentlicht - 15 Jan. 2008

ASJC Scopus Sachgebiete

Biochemie
Physikalische und Theoretische Chemie
Organische Chemie
Anorganische Chemie
Werkstoffchemie

Zugriff auf Dokument

10.1016/j.jorganchem.2007.10.053

Andere Dateien und Links

Link zur Publikation in Scopus

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

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.",

year = "2008",

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doi = "10.1016/j.jorganchem.2007.10.053",

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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

UR - https://www.scopus.com/pages/publications/37348999716

U2 - 10.1016/j.jorganchem.2007.10.053

DO - 10.1016/j.jorganchem.2007.10.053

M3 - Survey paper

AN - SCOPUS:37348999716

SN - 0022-328X

VL - 693

SP - 357

EP - 360

JO - Journal of Organometallic Chemistry

JF - Journal of Organometallic Chemistry

IS - 2

ER -