Room-Temperature Aqueous Suzuki–Miyaura Cross-Coupling

Apr 24, 2009 - for Suzuki-Miyaura Coupling of Sterically. Hindered Aryl Bromides. Takashi Hoshi,*,† Ippei Saitoh,‡ Taichi Nakazawa,‡. Toshio Suzuki ...

Highly Active, Recoverable, and ... Grasa, G. A.; Hillier, A. C.; Nolan, S. P. Org. Lett. 2001 ... (4) Recently, a highly active hydroxyapatite-supported Pd(II) catalyst.

Miyaura cross-coupling reaction has become a cornerstone of organic synthesis.1 Recent advances have significantly broadened the scope of the reaction, ...

... Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic. UniVersity, Hung Hom, Kowloon, Hong Kong [email protected].

Institute of Molecular and Biological Chemistry, Swiss Institute of Technology,. BCH CH-1015 Lausanne, .... A small library of ligands was tested, and it was found that the carbene .... Acknowledgment. We thank the Swiss National Science.

Oct 4, 2007 - hydroborated using the Snieckus hydroborating reagent (i-PP2-. BH),11 and the resulting organoborane intermediates were treated.

Jefferson D. Revell and A. Ganesan*. Combinatorial Centre of Excellence, Department of Chemistry,. UniVersity of Southampton, Southampton SO17 1BJ, ...

Richard J. K. Taylor*. Department of Chemistry, UniVersity of York, Heslington, York, YO10 5DD, U.K. [email protected]; [email protected]. Received September ...

The First General Palladium Catalyst for the Suzuki-Miyaura and Carbonyl. Enolate Coupling of Aryl Arenesulfonates. Hanh Nho Nguyen, Xiaohua Huang, and ...

Dec 11, 2008 - Department of Medicinal Chemistry, Merck Research Laboratories, Merck & Co., Inc.,. P.O. Box 2000, Rahway, New Jersey 07065-0900, and ...