1998

Thomas Mackewitz

Daniel Appella

Electronic Dependence of C−O Reductive Elimination from Palladium (Aryl)neopentoxide Complexes

R. A. Widenhoefer and Buchwald, S. L. “Electronic Dependence of C−O Reductive Elimination from Palladium (Aryl)neopentoxide Complexes”, J. Am. Chem. Soc., 1998, 120(26), 6504-6511.

A palladium-catalyzed strategy for the preparation of indoles: A novel entry into the Fischer indole synthesis

S. Wagaw, Yang, B. H. , and Buchwald, S. L. “A palladium-catalyzed strategy for the preparation of indoles: A novel entry into the Fischer indole synthesis”, J. Am. Chem. Soc., 1998, 120(26), 6621-6622.

Amine additives greatly expand the scope of asymmetric hydrosilylation of imines

X. Verdaguer, Lange, U. E. W. , and Buchwald, S. L. “Amine additives greatly expand the scope of asymmetric hydrosilylation of imines”, Angew. Chem. Int. Ed., 1998, 37(8), 1103-1107.

A general synthesis of end-functionalized oligoanilines via palladium-catalyzed amination

R. A. Singer, Sadighi, J. P. , and Buchwald, S. L. “A general synthesis of end-functionalized oligoanilines via palladium-catalyzed amination”, J. Am. Chem. Soc., 1998, 120(1), 213-214.

Palladium-catalyzed synthesis of monodisperse, controlled-length, and functionalized oligoanilines

J. P. Sadighi, Singer, R. A. , and Buchwald, S. L. “Palladium-catalyzed synthesis of monodisperse, controlled-length, and functionalized oligoanilines”, J. Am. Chem. Soc., 1998, 120(20), 4960-4976.

A highly active palladium catalyst system for the arylation of anilines

J. P. Sadighi, Harris, M. C. , and Buchwald, S. L. “A highly active palladium catalyst system for the arylation of anilines”, Tet. Lett., 1998, 39(30), 5327-5330.

Short Enantioselective Total Syntheses of the Piperidine Alkaloids (S)-Coniine and (2R,6R)-trans-Solenopsin A via Catalytic Asymmetric Imine Hydrosilylation

M. T. Reding and Buchwald, S. L. “Short Enantioselective Total Syntheses of the Piperidine Alkaloids (S)-Coniine and (2R,6R)-trans-Solenopsin A via Catalytic Asymmetric Imine Hydrosilylation”, J. Org. Chem., 1998, 63(18), 6344-6347.

A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides

D. W. Old, Wolfe, J. P. , and Buchwald, S. L. “A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides”, J. Am. Chem. Soc., 1998, 120(37), 9722-9723.

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