Suzuki-Miyaura reaction of chloroarenes using Pd(PPh3) 4 as catalyst

Thies Thiemann; Yasuko Tanaka; Soleiman Hisaindee; Maitha Kaabi

doi:10.3184/030823410X12624523028293

Suzuki-Miyaura reaction of chloroarenes using Pd(PPh₃) ₄ as catalyst

Thies Thiemann, Yasuko Tanaka, Soleiman Hisaindee, Maitha Kaabi

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Abstract

The reactivity of a number of chloroarenes was investigated and chloro-nitroarenes were found to undergo facile arylation with Pd(PPh ₃)₄ / [Pd(PPh₃)₂Cl ₂/n.PPh₃] as catalyst. Furthermore, 4-chlorobenzaldehyde underwent arylation under the conditions, albeit with a higher catalyst loading.

Original language	English
Pages (from-to)	34-38
Number of pages	5
Journal	Journal of Chemical Research
Issue number	1
DOIs	https://doi.org/10.3184/030823410X12624523028293
Publication status	Published - 2010

Keywords

Nitrochlorobenzenes
Suzuki-miyaura cross-coupling
Tetrakis(triphenylphosphino)palladium(0)

ASJC Scopus subject areas

General Chemistry

Access to Document

10.3184/030823410X12624523028293

Cite this

@article{b499fc38b341441fa9f6aeabfd204296,

title = "Suzuki-Miyaura reaction of chloroarenes using Pd(PPh3) 4 as catalyst",

abstract = "The reactivity of a number of chloroarenes was investigated and chloro-nitroarenes were found to undergo facile arylation with Pd(PPh 3)4 / [Pd(PPh3)2Cl 2/n.PPh3] as catalyst. Furthermore, 4-chlorobenzaldehyde underwent arylation under the conditions, albeit with a higher catalyst loading.",

keywords = "Nitrochlorobenzenes, Suzuki-miyaura cross-coupling, Tetrakis(triphenylphosphino)palladium(0)",

author = "Thies Thiemann and Yasuko Tanaka and Soleiman Hisaindee and Maitha Kaabi",

year = "2010",

doi = "10.3184/030823410X12624523028293",

language = "English",

pages = "34--38",

journal = "Journal of Chemical Research",

issn = "0308-2342",

publisher = "Science Reviews Ltd",

number = "1",

}

TY - JOUR

T1 - Suzuki-Miyaura reaction of chloroarenes using Pd(PPh3) 4 as catalyst

AU - Thiemann, Thies

AU - Tanaka, Yasuko

AU - Hisaindee, Soleiman

AU - Kaabi, Maitha

PY - 2010

Y1 - 2010

N2 - The reactivity of a number of chloroarenes was investigated and chloro-nitroarenes were found to undergo facile arylation with Pd(PPh 3)4 / [Pd(PPh3)2Cl 2/n.PPh3] as catalyst. Furthermore, 4-chlorobenzaldehyde underwent arylation under the conditions, albeit with a higher catalyst loading.

AB - The reactivity of a number of chloroarenes was investigated and chloro-nitroarenes were found to undergo facile arylation with Pd(PPh 3)4 / [Pd(PPh3)2Cl 2/n.PPh3] as catalyst. Furthermore, 4-chlorobenzaldehyde underwent arylation under the conditions, albeit with a higher catalyst loading.

KW - Nitrochlorobenzenes

KW - Suzuki-miyaura cross-coupling

KW - Tetrakis(triphenylphosphino)palladium(0)

UR - http://www.scopus.com/inward/record.url?scp=77949379124&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=77949379124&partnerID=8YFLogxK

U2 - 10.3184/030823410X12624523028293

DO - 10.3184/030823410X12624523028293

M3 - Article

AN - SCOPUS:77949379124

SN - 0308-2342

SP - 34

EP - 38

JO - Journal of Chemical Research

JF - Journal of Chemical Research

IS - 1

ER -