Synthesis of Pyrrolo[2,1,5-cd]indolizines through Dehydrogenative Heck Annelation of Indolizines with Diaryl Acetylenes Using Dioxygen as an Oxidant

DOI: 10.1021/ol503681n

Synthesis of 1H-Indazoles and 1H-Pyrazoles via FeBr3/O2 Mediated Intramolecular C–H Amination

One-pot synthesis of carbazoles from cyclohexanones and arylhydrazine hydrochlorides under metal-free conditions

Pd-Catalyzed Synthesis of Aryl Amines via Oxidative Aromatization of Cyclic Ketones and Amines with Molecular Oxygen

Synthesis of Oxazoles through Copper-Mediated Aerobic Oxidative Dehydrogenative Annulation and Oxygenation of Aldehydes and Amines

Palladium(II)-Catalyzed Tandem Cyclization/C–H Functionalization of Alkynes for the Synthesis of Functionalized Indoles

Palladium-Catalyzed Oxidation of Unsaturated Hydrocarbons Using Molecular Oxygen

Transition metal based catalysts in the aerobic oxidation of alcohols

Green Chem., 2012, 14, 547-564

Synthesis of Densely Substituted α,β,γ,δ-Dienones via the PdII-Catalyzed Allylation, H-Migration, and Aerobic Oxidative δ-Hydride Elimination Cascade

Org. Lett., 2012, DOI: 10.1021/ol203444g

Overcoming the “Oxidant Problem”: Strategies to Use O2 as the Oxidant in Organometallic C–H Oxidation Reactions Catalyzed by Pd (and Cu)

Oxidation reactions are key transformations in organic chemistry because they can increase chemical complexity and incorporate heteroatom substituents into carbon-based molecules. This principle is manifested in the conversion of petrochemical feedstocks into commodity chemicals and in the synthesis of fine chemicals, pharmaceuticals, and other complex organic molecules. The utility and function of these molecules correlate directly with the presence and specific placement of oxygen and nitrogen heteroatoms and other functional groups within the molecules.

Methods for selective oxidation of C–H bonds have expanded significantly over the past decade, and their role in the synthesis of organic chemicals will continue to increase. Our group’s contributions to this field are linked to our broader interest in the development and mechanistic understanding of aerobic oxidation reactions. Molecular oxygen (O2) is the ideal oxidant. Its low cost and lack of toxic byproducts make it a highly appealing reagent that can address key “green chemistry” priorities in industry. With strong economic and environmental incentives to use O2, the commmodity chemicals industry often uses aerobic oxidation reactions. In contrast, O2 is seldom used to prepare more-complex smaller-volume chemicals, a limitation that reflects, in part, the limited synthetic scope and utility of existing aerobic reactions.

Pd-catalyzed reactions represent some of the most versatile methods for selective C–H oxidation, but they often require stoichiometric transition-metal or organic oxidants, such as CuII, AgI, or benzoquinone. This Account describes recent strategies that we have identified to use O2 as the oxidant in these reactions. In Pd-catalyzed C–H oxidation reactions that form carbon-heteroatom bonds, the stoichiometric oxidant is often needed to promote difficult reductive elimination steps in the catalytic mechanism. To address this challenge, we have identified new ancillary ligands for Pd that promote reductive elimination, or replaced Pd with a Cu catalyst that undergoes facile reductive elimination from a CuIII intermediate. Both strategies have enabled O2 to be used as the sole stoichiometric oxidant in the catalytic reactions. C–H oxidation reactions that form the product via β-hydride or C–C reductive elimination steps tend to be more amenable to the use of O2. The use of new ancillary ligands has also overcome some of the limitations in these methods. Mechanistic studies are providing insights into some (but not yet all) of these advances in catalytic reactivity.

Copper-catalyzed direct oxidative synthesis of α-ketoamides from aryl methyl ketones, amines, and molecular oxygen

A novel and efficient copper-catalyzed direct oxidative synthesis of α-ketoamides from aryl methyl ketones, amines, and molecular oxygen has been developed under mild and neat conditions. ¹⁸O labeling experiments revealed that both oxygen atoms of the α-ketoamides derived from molecular oxygen.

Palladium Catalysed Aerobic Dehydrogenation of C[BOND]H Bonds in Cyclohexanones

Palladium Catalysed Aerobic Dehydrogenation of CH Bonds in Cyclohexanones

DOI: 10.1002/cctc.201100361

Simple and Sustainable Copper–O2 Chemistry towards High-Value Products