Suzuki-Miyaura cross-coupling of aryl chlorides in water using ligandless palladium on activated carbon

Morten Lysén; Klaus Köhler

doi:10.1055/s-2005-869877

Suzuki-Miyaura cross-coupling of aryl chlorides in water using ligandless palladium on activated carbon

Morten Lysén
, Klaus Köhler

Professur für Anorganische Chemie

Publikation: Beitrag in Fachzeitschrift › Artikel › Begutachtung

75 Zitate (Scopus)

Abstract

Aqueous reaction conditions that activate various aryl chlorides in Suzuki-Miyaura cross-coupling have been developed. These environment friendly conditions utilize ligandless Pd/C (Pd concentrations 0.2-2 mol%) that allow easy separation of the catalyst at the end of the reaction.

Originalsprache	Englisch
Seiten (von - bis)	1671-1674
Seitenumfang	4
Fachzeitschrift	Synlett
Ausgabenummer	11
DOIs	https://doi.org/10.1055/s-2005-869877
Publikationsstatus	Veröffentlicht - 7 Juli 2005

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title = "Suzuki-Miyaura cross-coupling of aryl chlorides in water using ligandless palladium on activated carbon",

abstract = "Aqueous reaction conditions that activate various aryl chlorides in Suzuki-Miyaura cross-coupling have been developed. These environment friendly conditions utilize ligandless Pd/C (Pd concentrations 0.2-2 mol\%) that allow easy separation of the catalyst at the end of the reaction.",

keywords = "Aryl chlorides, Biaryls, Cross-coupling, Palladium, Water",

author = "Morten Lys{\'e}n and Klaus K{\"o}hler",

year = "2005",

month = jul,

day = "7",

doi = "10.1055/s-2005-869877",

language = "English",

pages = "1671--1674",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

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T1 - Suzuki-Miyaura cross-coupling of aryl chlorides in water using ligandless palladium on activated carbon

AU - Lysén, Morten

AU - Köhler, Klaus

PY - 2005/7/7

Y1 - 2005/7/7

N2 - Aqueous reaction conditions that activate various aryl chlorides in Suzuki-Miyaura cross-coupling have been developed. These environment friendly conditions utilize ligandless Pd/C (Pd concentrations 0.2-2 mol%) that allow easy separation of the catalyst at the end of the reaction.

AB - Aqueous reaction conditions that activate various aryl chlorides in Suzuki-Miyaura cross-coupling have been developed. These environment friendly conditions utilize ligandless Pd/C (Pd concentrations 0.2-2 mol%) that allow easy separation of the catalyst at the end of the reaction.

KW - Aryl chlorides

KW - Biaryls

KW - Cross-coupling

KW - Palladium

KW - Water

UR - https://www.scopus.com/pages/publications/22244463212

U2 - 10.1055/s-2005-869877

DO - 10.1055/s-2005-869877

M3 - Article

AN - SCOPUS:22244463212

SN - 0936-5214

SP - 1671

EP - 1674

JO - Synlett

JF - Synlett

IS - 11

ER -

Suzuki-Miyaura cross-coupling of aryl chlorides in water using ligandless palladium on activated carbon

Abstract

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