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Palladium-Catalyzed ortho-Alkylation of Iodoarenes Enabled by a Cooperative Cycloolefin Ligand and a Bulky Trialkylphosphine.

We recently achieved ortho-alkylation of iodoarenes utilizing a dual-ligand catalytic system that effectively combines palladium/olefin ligand cooperative catalysis with reversible C(sp2)–I reductive elimination enabled by a bulky trialkylphosphine …

Chiral Ligands for Palladium-Catalyzed Coordination-Assisted Enantioselective C(sp<sup>3</sup>)-H Functionalization Reactions (Invited Review).<br>手性配体在钯催化配位辅助对映选择性C(sp<sup>3</sup>)-H键官能团化反应中的应用(中文综述)

Enantioselective C(sp3)-H functionalization reactions have emerged as a powerful and straightforward strategy in the construction of chiral molecules. Palladium, highlighted by its remarkable reactivity, versatility, and functional group tolerance, …

Dual Ligand Enabled Pd-Catalyzed *Ortho*-Alkylation of Iodoarenes.

The synthesis of complex polysubstituted aromatic molecules from simple precursors is a central goal in organic chemistry. In this study, we developed an approach for the ortho-alkylation of iodoarenes utilizing a dual ligand catalytic system. By …

Thio-Cycloolefin Ligand Enabled Distal Methylation in the Catellani-Type Reaction via a Six-Membered Palladacycle.

TThe Catellani reaction, also known as the Pd/norbornene catalysis, is a potent method for synthesizing multisubstituted arenes through the ortho-functionalization/ipso-termination process of haloarenes. This chemistry relies heavily on the formation …

Unveiling the Mechanistic Role of Chiral Palladacycles in Pd(II)-Catalyzed Enantioselective C(sp<sup>3</sup>)-H Functionalization.

Palladium-catalyzed enantioselective C(sp3)-H functionalization reactions has attracted considerable attention due to its ability for the synthesis of enantiomerically enriched molecules and stimulation of novel retrosynthetic disconnections. …

Thio-Cyclopentene Ligands for Catellani-Type Reactions.

We have developed thio-cyclopentene ligands for Pd(II) catalysis, which could substitute norbornene or its derivatives to promote Catellani-type reactions. These ligands enabled generic palladium/olefin cooperative catalysis for the first time, and …

Ligand-Enabled Palladium(II)-Catalyzed γ-C(sp<sup>3</sup>)−H Arylation of Primary Aliphatic Amines.

Amines are common scaffolds in bioactive molecules as well as building blocks for chemical synthesis. Despite significant advances in palladium-catalyzed C(sp3)−H functionalization of amines over the past decades, it remains challenging to perform …

Ligand-Enabled Pd(II)-Catalyzed Enantioselective β-C(sp<sup>3</sup>)-H Arylation of Aliphatic Tertiary Amides.

Amide is a widespread functional group in organic and bioorganic chemistry, and it is valuable to achieve stereoselective C(sp3)-H functionalization in amide molecules. Pd(II) catalysis has been prevalently used in the C-H activation chemistry in the …

Functionalized Cycloolefin Ligand as a Solution to *Ortho*-Constraint in the Catellani-Type Reaction.

The Catellani reaction, i.e. the Pd/NBE cooperative catalysis, has been evolved into a versatile approach to multisubstituted arenes via the ortho-functionalization/ipso-termination process of a haloarene. Despite significant advances over the past …

Hybrid Cycloolefin Ligands for Palladium/Olefin Cooperative Catalysis.

Engineering of molecular catalysts in homogeneous catalysis enables new catalytic modes, leading to efficient synthetic transformations. In this regard, design of ligands for transition-metal catalysis has played a major role. In transition metal …