2007
DOI: 10.1016/j.tet.2007.04.016
|View full text |Cite
|
Sign up to set email alerts
|

Copper(I)-catalysed homo-coupling of aryldiazonium salts: synthesis of symmetrical biaryls

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

1
22
0

Year Published

2008
2008
2020
2020

Publication Types

Select...
8
2

Relationship

0
10

Authors

Journals

citations
Cited by 45 publications
(23 citation statements)
references
References 54 publications
1
22
0
Order By: Relevance
“…Recently, a few reports on the homo-coupling of arenediazonium salts have appeared, but the scope of these reactions was limited to biaryl synthesis. 18,19 Only few reports described the use of cross-coupling reaction to generate polyphenyls.…”
Section: -3mentioning
confidence: 99%
“…Recently, a few reports on the homo-coupling of arenediazonium salts have appeared, but the scope of these reactions was limited to biaryl synthesis. 18,19 Only few reports described the use of cross-coupling reaction to generate polyphenyls.…”
Section: -3mentioning
confidence: 99%
“…One of the well-recognized mechanisms for Ullmann reaction [6,7] (Scheme 1, abbreviated as 0/2/4) involves consecutive oxidative addition steps of aryl halide on Pd(0) and Pd(II) species, respectively. The resulting Pd(IV) species is very unstable and readily undergoes reductive elimination to form Pd(II) species.…”
Section: Introductionmentioning
confidence: 99%
“…Thus efficient aryl-aryl bond forming reactions have been the theme of many research papers [4][5][6][7][8][9][10][11][12][13][14]. Symmetrical biaryl compounds are traditionally prepared by the Ullmann homo-coupling reaction, which involves the condensation of aryl halide molecules by a stoichiometric amount of copper at very high (>200°C) temperatures [15].…”
Section: Introductionmentioning
confidence: 99%