Synlett

A mixed naphthyl-phenyl phosphine ligand motif for Suzuki, Heck, and hydrodehalogenation reactions

OM Demchuk, B Yoruk, T Blackburn, V Snieckus

Index: Demchuk, Oleg M.; Yoruk, Bilge; Blackburn, Tom; Snieckus, Victor Synlett, 2006 , # 18 p. 2908 - 2913

Full Text: HTML

Citation Number: 12

Abstract

Abstract Nap-Phos, representing a new naphthyl-phenyl biaryl-type phosphine ligand class and available by a short synthesis (4 steps, 71% overall yield), effectively catalyzes the Suzuki-Miyaura (including highly hindered cases), hydrodehalogenation, and Heck reactions.

Related Articles:

Cooperative catalysis of palladium nanoparticles and cobalt oxide support for formylation of aryl iodides under syngas atmosphere

[Applied Catalysis A: General, , vol. 469, p. 146 - 152]

Palladium-catalyzed hydrodehalogenation of aryl halides using paraformaldehyde as the hydride source: high-throughput screening by paper-based colorimetric …

[Pyo, Ayoung; Kim, Sudeok; Kumar, Manian Rajesh; Byeun, Aleum; Eom, Min Sik; Han, Min Su; Lee, Sunwoo Tetrahedron Letters, 2013 , vol. 54, # 38 p. 5207 - 5210]

Orthogonal Cu-and Pd-based catalyst systems for the O-and N-arylation of aminophenols

[Journal of the American Chemical Society, , vol. 131, # 47 p. 17423 - 17429]

Activity Stabilization of Ga-MFI Zeolite Catalyst Modified by Chemical Vapor Deposition.

[Bulletin of the Chemical Society of Japan, , vol. 69, # 2 p. 469 - 472]

On the mechanism of palladium-catalyzed coupling of haloaryls to biaryls in water with zinc

[Organic Letters, , vol. 2, # 2 p. 211 - 214]

More Articles...