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Development of Hetero-Vinylbenziodoxolone Reagents for Applications in Synthetic Methodology and Biomolecule Functionalization

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Development of Hetero-Vinylbenziodoxolone Reagents for Applications in Synthetic Methodology and Biomolecule Functionalization

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Diverting the 5-exo-Trig Oxypalladation to Formally 6-endo-Trig Fluorocycloetherification Product through 1,2-O/Pd(IV) Dyotropic Rearrangement

Photochemical Alkynylations with Hypervalent Iodine Reagents

Pd(II)-Catalyzed Aminoacetoxylation of Alkenes Via Tether Formation

Radical Alkynylations with EthynylBenziodoXolones: From Photocatalysis to Direct Excitation

Rh-catalyzed C-H Bond Heteroarylation with Hypervalent Iodine Reagents and Pd-Catalyzed Tethered Functionalizations of Carbon-Carbon Multiple Bonds

Exploring Photoredox-Catalyzed (Re)functionalizations with Core-Modified Benziodoxolones

Development of metal-organic frameworks based on N-heterocyclic ligands

Oxidase-Type C-H/C-H Coupling Using an Isoquinoline-Derived Organic Photocatalyst

Ring-Opening Reactions of Aminocyclopropanes and Aminocyclobutanes

Modular Synthesis of Benzocyclobutenes via Pd(II)-Catalyzed Oxidative [2+2] Annulation of Arylboronic Acids with Alkenes

Access to Vinyl Ethers and Ketones with Hypervalent Iodine Reagents as Oxy-Allyl Cation Synthetic Equivalents