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Ligand-Controlled Palladium-Catalyzed Asymmetric [4+3] and [2+3] Annulation Reactions of Spirovinylcyclopropyl Oxindoles with o -Quinone Methides.

Xiyuan ZhangCong ZhangBo JiangYanfeng GaoXiufang XuZhiwei Miao
Published in: Organic letters (2022)
We herein report regiodivergent ligand-controlled palladium-catalyzed asymmetric cycloaddition reactions between spirovinylcyclopropyl oxindoles and o -quinone methides. Specifically, by using the chiral P,P-ligand Segphos ( L5 ), we obtained various spirooxindole-3,4-benzo[ b ]oxepanes in moderate to good yields with excellent enantioselectivities via [4+3] cycloaddition reactions. In contrast, reactions involving Trost's ligand ( L7 ) showed different regio- and stereoselectivities, affording bispirooxindole heterocyclic compounds in good yields via [2+3] cycloaddition reactions.
Keyphrases
  • magnetic resonance
  • computed tomography
  • solid state