Palladium-catalyzed trifluoroacetate-promoted mono-arylation of the β-methyl group of alanine at room temperature: synthesis of β-arylated α-amino acids through sequential C–H functionalization

Experimental and computational studies on the mechanism of the Pd-catalyzed C(sp3)–H γ-arylation of amino acid derivatives assisted by the 2-pyridylsulfonyl group

10.1039/C4SC00848K

Direct allylation of aromatic and α,β-unsaturated carboxamides under ruthenium catalysis

Manganese(III)-Catalyzed Oxidative Cyclization of Aryl 1-Cyanoalk-5-ynyl Ketone Systems: A Convenient and General Approach to Cyclopenta[b]naphthalene Derivatives

DOI: 10.1002/adsc.201400257

Rhodium(III)-Catalyzed Intramolecular Redox-Neutral Annulation of Tethered Alkynes: Formal Total Synthesis of (±)-Goniomitine

DOI: 10.1002/chem.201403973

Rhodium(III)-Catalyzed Intramolecular Redox-Neutral Annulation of Tethered Alkynes: Formal Total Synthesis of (±)-Goniomitine - Zhou - 2014 - Chemistry - A European Journal - Wiley Online Library

DOI: 10.1002/chem.201403973

Iridium(III)-Catalyzed C[BOND]H Amidation of Arylphosphoryls Leading to a P-Stereogenic Center

DOI: 10.1002/chem.201404151

Advancements in Catalytic Asymmetric Intermolecular Ene-Type Reactions

DOI: 10.1055/s-0034-1378528

Nickel(II)-Catalyzed Direct Arylation of C–H Bonds in Aromatic Amides Containing an 8-Aminoquinoline Moiety as a Directing Group

DOI: 10.1021/jo501697n

Palladium-Catalyzed Intramolecular Oxidative Coupling Involving Double C(sp2)–H Bonds for the Synthesis of Annulated Biaryl Sultams

10.1021/jo5011334

Synthesis of Sulfur-Bridged Polycycles via Pd-Catalyzed Dehydrogenative Cyclization

Rhodium(III)-Catalyzed C–C Bond Formation of Quinoline N-Oxides at the C-8 Position under Mild Conditions

DOI: 10.1021/ol502173d

Cobalt-Catalyzed Direct Carbonylation of Aminoquinoline Benzamides

DOI: 10.1021/ol502007t

Cobalt-Catalyzed, Aminoquinoline-Directed Coupling of sp2 C–H Bonds with Alkenes

DOI: 10.1021/ol502005g

A General Synthesis of Ynones from Aldehydes via Oxidative C–C bond Cleavage under Aerobic Conditions

DOI: 10.1021/ja506352b