An efficient catalyst for the synthesis of ortho-substituted biaryls by the Suzuki cross-coupling: Triphenylphosphine adduct of cyclopalladated ferrocenylimine
H Li, Y Wu, W Yan
Index: Li, Hong; Wu, Yangjie; Yan, Weibo Journal of Organometallic Chemistry, 2006 , vol. 691, p. 5688 - 5696
Full Text: HTML
Citation Number: 12
Abstract
The air and moisture stable triphenylphosphine adduct of cyclopalladated ferrocenylimine 2 has been successfully used in palladium-catalyzed Suzuki cross-coupling for the synthesis of ortho-substituted biaryls in air. In the presence of 0.05 mol% of 2 as catalyst and 3
Related Articles:
Pd-catalysed asymmetric Suzuki–Miyaura reactions using chiral mono-and bidentate phosphorus ligands
[Castillo, Angelica Balanta; Perandones, Bernabe F.; Zangrando, Ennio; Gladiali, Serafino; Godard, Cyril; Claver, Carmen Journal of Organometallic Chemistry, 2013 , vol. 743, p. 31 - 36]
[Castanet, Anne-Sophie; Colobert, Francoise; Broutin, Pierre-Emmanuel; Obringer, Michel Tetrahedron Asymmetry, 2002 , vol. 13, # 6 p. 659 - 665]
[Tetrahedron Asymmetry, , vol. 13, # 6 p. 659 - 665]
[Organic Process Research and Development, , vol. 7, # 3 p. 379 - 384]