2-Aminobiphenyl palladacycles: The "most powerful" precatalysts in C-C and C-heteroatom cross-couplings

Alexandre Bruneau; Maxime Roche; Mouad Alami; Samir Messaoudi

doi:10.1021/cs502011x

2-Aminobiphenyl palladacycles: The "most powerful" precatalysts in C-C and C-heteroatom cross-couplings

Alexandre Bruneau
, Maxime Roche
, Mouad Alami
, Samir Messaoudi

Université Paris-Saclay

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

159 Citations (Scopus)

Résumé

New approaches to the Pd-catalysis employing palladacycle precatalysts have been recently developed. Breakthroughs in this area using 2-aminobiphenyl palladacycle precatalysts are highlighted. High reactivity and selectivity are achieved for the C-C and C-heteroatom bond formation under mild reaction conditions. (Figure Presented).

langue originale	Anglais
Pages (de - à)	1386-1396
Nombre de pages	11
journal	ACS Catalysis
Volume	5
Numéro de publication	2
Les DOIs	https://doi.org/10.1021/cs502011x
état	Publié - 6 févr. 2015
Modification externe	Oui

Accès au document

10.1021/cs502011x

Contient cette citation

@article{cdfcfc0ef5e5475aa0a1a5d725c0a09e,

title = "2-Aminobiphenyl palladacycles: The {"}most powerful{"} precatalysts in C-C and C-heteroatom cross-couplings",

abstract = "New approaches to the Pd-catalysis employing palladacycle precatalysts have been recently developed. Breakthroughs in this area using 2-aminobiphenyl palladacycle precatalysts are highlighted. High reactivity and selectivity are achieved for the C-C and C-heteroatom bond formation under mild reaction conditions. (Figure Presented).",

keywords = "C-C and C-heteroatom bonds formation, catalysis, cross-couplings, palladacycles, precatalysts",

author = "Alexandre Bruneau and Maxime Roche and Mouad Alami and Samir Messaoudi",

note = "Publisher Copyright: {\textcopyright} 2015 American Chemical Society.",

year = "2015",

month = feb,

day = "6",

doi = "10.1021/cs502011x",

language = "English",

volume = "5",

pages = "1386--1396",

journal = "ACS Catalysis",

issn = "2155-5435",

publisher = "American Chemical Society",

number = "2",

}

TY - JOUR

T1 - 2-Aminobiphenyl palladacycles

T2 - The "most powerful" precatalysts in C-C and C-heteroatom cross-couplings

AU - Bruneau, Alexandre

AU - Roche, Maxime

AU - Alami, Mouad

AU - Messaoudi, Samir

PY - 2015/2/6

Y1 - 2015/2/6

N2 - New approaches to the Pd-catalysis employing palladacycle precatalysts have been recently developed. Breakthroughs in this area using 2-aminobiphenyl palladacycle precatalysts are highlighted. High reactivity and selectivity are achieved for the C-C and C-heteroatom bond formation under mild reaction conditions. (Figure Presented).

AB - New approaches to the Pd-catalysis employing palladacycle precatalysts have been recently developed. Breakthroughs in this area using 2-aminobiphenyl palladacycle precatalysts are highlighted. High reactivity and selectivity are achieved for the C-C and C-heteroatom bond formation under mild reaction conditions. (Figure Presented).

KW - C-C and C-heteroatom bonds formation

KW - catalysis

KW - cross-couplings

KW - palladacycles

KW - precatalysts

U2 - 10.1021/cs502011x

DO - 10.1021/cs502011x

M3 - Article

AN - SCOPUS:84922705329

SN - 2155-5435

VL - 5

SP - 1386

EP - 1396

JO - ACS Catalysis

JF - ACS Catalysis

IS - 2

ER -

2-Aminobiphenyl palladacycles: The "most powerful" precatalysts in C-C and C-heteroatom cross-couplings

Résumé

Accès au document

Empreinte digitale

Contient cette citation