ol7b01303_si_003.cif (428.16 kB)
Synthetic Study of Phainanoids. Highly Diastereoselective Construction of the 4,5-Spirocycle via Palladium-Catalyzed Intramolecular Alkenylation
datasetposted on 2017-05-19, 13:20 authored by Jiaxin Xie, Jianchun Wang, Guangbin Dong
An efficient strategy to synthesize the western part of phainanoids is reported. The benzofuranone-based 4,5-spirocyclic motif is constructed diastereoselectively via a palladium-catalyzed intramolecular alkenylation. The computational study suggests that the remarkably high diastereoselectivity is attributed to the stabilizing interaction between the 2′ carbonyl moiety and the palladium catalyst in the favored transition state.
motifphainanoidcarbonyldiastereoselectivitymoietySpirocyclestrategySynthetic Studytransition statepalladium-catalyzed intramolecular alkenylationspirocyclicPalladium-Catalyzed Intramolecular AlkenylationDiastereoselective Constructionbenzofuranone-basedinteractionPhainanoidpalladium catalystdiastereoselectively