2002

Monocyclopentadienyltitanium Aryloxide Complexes: Preparation, Characterization, and Application in Cyclization Reactions

S. J. Sturla and Buchwald, S. L. “Monocyclopentadienyltitanium Aryloxide Complexes: Preparation, Characterization, and Application in Cyclization Reactions”, Organometallics, 2002, 21(4), 739-748.

Cobalt−Phosphite-Catalyzed Asymmetric Pauson−Khand Reaction

S. J. Sturla and Buchwald, S. L. “Cobalt−Phosphite-Catalyzed Asymmetric Pauson−Khand Reaction”, J. Org. Chem., 2002, 67(10), 3398-3403.

Preparation, Crystal Structure Analysis, and Catalytic Application of [(S)-BINAP]Ni(COD) and [(S)-BINAP]NiBr2

D. J. Spielvogel, Davis, W. M. , and Buchwald, S. L. “Preparation, Crystal Structure Analysis, and Catalytic Application of [(S)-BINAP]Ni(COD) and [(S)-BINAP]NiBr2”, Organometallics, 2002, 21(18), 3833-3836.

Nickel-BINAP Catalyzed Enantioselective α-Arylation of α-Substituted γ-Butyrolactones

D. J. Spielvogel and Buchwald, S. L. “Nickel-BINAP Catalyzed Enantioselective α-Arylation of α-Substituted γ-Butyrolactones”, J. Am. Chem. Soc., 2002, 124(14), 3500-3501.

Mechanistic Insights into the Pd(BINAP)-Catalyzed Amination of Aryl Bromides: Kinetic Studies under Synthetically Relevant Conditions

U. K. Singh, Strieter, E. R. , Blackmond, D. G. , and Buchwald, S. L. “Mechanistic Insights into the Pd(BINAP)-Catalyzed Amination of Aryl Bromides: Kinetic Studies under Synthetically Relevant Conditions”, J. Am. Chem. Soc., 2002, 124(47), 14104-14114.

An Annulative Approach to Highly Substituted Indoles: Unusual Effect of Phenolic Additives on the Success of the Arylation of Ketone Enolates

J. L. Rutherford, Rainka, M. P. , and Buchwald, S. L. “An Annulative Approach to Highly Substituted Indoles: Unusual Effect of Phenolic Additives on the Success of the Arylation of Ketone Enolates”, J. Am. Chem. Soc., 2002, 124(51), 15168-15169.

Copper-Catalyzed Coupling of Alkylamines and Aryl Iodides: An Efficient System Even in an Air Atmosphere

F. Yee Kwong, Klapars, A. , and Buchwald, S. L. “Copper-Catalyzed Coupling of Alkylamines and Aryl Iodides: An Efficient System Even in an Air Atmosphere”, Org. Lett., 2002, 4(4), 581-584.

A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols

F. Yee Kwong and Buchwald, S. L. “A General, Efficient, and Inexpensive Catalyst System for the Coupling of Aryl Iodides and Thiols”, Org. Lett., 2002, 4(20), 3517-3520.

A General and Efficient Copper Catalyst for the Amidation of Aryl Halides

A. Klapars, Huang, X. , and Buchwald, S. L. “A General and Efficient Copper Catalyst for the Amidation of Aryl Halides”, J. Am. Chem. Soc., 2002, 124(25), 7421-7428.

Copper-Catalyzed Halogen Exchange in Aryl Halides: An Aromatic Finkelstein Reaction

A. Klapars and Buchwald, S. L. “Copper-Catalyzed Halogen Exchange in Aryl Halides: An Aromatic Finkelstein Reaction”, J. Am. Chem. Soc., 2002, 124(50), 14844-14845.

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