New Dimensions of Bronsted Base Catalyzed Carbon-Carbon Bond-Forming Reactions

Abstract

Catalytic carbon-carbon bond-forming reactions of weakly acidic carbon pronucleophiles (p K ain DMSO ≥30) were developed using strong alkaline metal Bronsted bases as catalysts. Not only weakly acidic amides, esters, nitriles, sulfonamides without any activating group, and alkyl azaarenes, but also alkyl arenes such as toluene, were applicable for the reactions, which are difficult to be applied in typical Bronsted base catalyzed reactions. Expansion to enantioselective reactions was also revealed to be possible. The reactions are atom economical and require only inexpensive alkaline metals rather than precious transition metals. 1 Introduction 2 Catalytic Direct-Type Addition Reactions of Weakly Acidic Carbonyl and Related Pronucleophiles 3 Catalytic Direct-Type Addition Reactions of Alkyl Azaarenes 4 Catalytic Direct-Type Addition Reactions of Alkyl Arenes 5 Conclusion.