Reported herein is a novel palladium-catalyzed [2+ 2+ 1] domino annulation of 3-
iodochromones, bridged olefins, and dimethyl squarate allowing the construction of …

A palladium-catalyzed three-component [2+ 3+ 1] domino annulation among 3-
iodochromones, α-bromoacetophenones, and norbornene is presented, affording various …

A novel palladium-catalyzed three-component reaction of 3-iodochromones with bridged
olefins and aziridine is described, which employs a [2+ 2+ 1] domino annulation strategy to …

A palladium-catalyzed [2+ 2+ 1] domino annulation of 3-iodochromones, α-bromo carbonyl
compounds, and tetracyclododecene (TCD) is described. This approach provides a facile …

Abstract A palladium‐catalyzed [2+ 2+ 1] annulation among 3‐iodochromones, benzyl
bromides, and norbornene has been developed. This annulation consists of a domino …

Chiral polycyclic chromanones are important heterocyclic frameworks that constitute the
core structures of many natural products and bioactive molecules. As starting materials, the …

Herein we report a palladium-catalyzed [2+ 2+ 1] annulation among 3-iodochromones,
bridged olefins, and cyclopropenone, giving a variety of chromone fused cyclopentanones …

A Pd-catalyzed domino process involving a double norbornene insertion/annulation reaction
was developed for the expeditious synthesis of overcrowded olefins. In this one-pot reaction …

A highly stereoselective triple domino reaction for the synthesis of functionalized tricyclic
chromane scaffolds has been developed. A secondary amine-catalyzed domino …

An efficient Pd-catalyzed domino reaction of α, α-dialkyl-(2-bromoaryl) methanols to 6, 6-
dialkyl-6 H-benzo [c] chromenes is presented. Their formation can be explained via a five …