Mechanism of palladium-catalyzed allylic substitution of tertiary allylic carbonates with sodium sulfinates: unusual bifunctional nucleophile-enabled inner-sphere pathway and origin of regio- and enantioselectivities

Palladium-catalyzed allylic sulfonylation of tertiary allylic carbonates with sodium sulfinates provides a first general asymmetric approach towards the synthesis of sterically encumbered α,α-disubstituted allylic sulfones. In this report, density functional theory calculations have been performed t...

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Detalles Bibliográficos
Autores: Wu, Hongli, Wu, Botao, Kleij, Arjan W., Huang, Genping
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2024
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2072/537488
Acceso en línea:http://hdl.handle.net/2072/537488
https://doi.org/10.1039/D3CY01493B
Access Level:acceso abierto
Palabra clave:Química
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Descripción
Sumario:Palladium-catalyzed allylic sulfonylation of tertiary allylic carbonates with sodium sulfinates provides a first general asymmetric approach towards the synthesis of sterically encumbered α,α-disubstituted allylic sulfones. In this report, density functional theory calculations have been performed to establish a detailed reaction mechanism that sheds light on the origin of the regio- and enantioselectivities. The computations reveal that C–S bond formation via the outer-sphere nucleophilic attack is kinetically not feasible, and does not reproduce the experimentally observed high branched type regioselectivity. Instead, the sulfonate nucleophile was found to play a bifunctional role during the C–S bond formation stage. The O-atom acts as a chelating group for the metal center to facilitate the nucleophilic attack by the S-atom, enabling C–S bond formation through a unique inner-sphere manifold that involves a six-membered chair-like transition state. The experimentally observed regio- and enantioselectivities are rationalized well with this mechanistic scenario that features steric and electronic effects, C–H---O hydrogen bonding and C–H---π interactions.