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- W2950542108 abstract "A practical method for a facile entry to structurally unique ring-fused dihydroazepine has been developed using 1-sulfonyl-1,3-dienyltriazole as starting materials. Driven by ring strain release of cyclopropyl group, a rhodium-catalyzed α-imino carbenoid formation–cyclopropanation–aza-Cope rearrangement cascade takes place efficiently in a single operation. Substitution effects on yield and diastereoselectivity are also explored." @default.
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- W2950542108 date "2014-12-03" @default.
- W2950542108 modified "2023-10-18" @default.
- W2950542108 title "Ring-Strain-Driven Catalytic Carbene Formation–Cyclopropanation–Aza-Cope Rearrangement Cascade: A Facile Entry to Fused Dihydroazepines from 1,3-Dienyltriazoles" @default.
- W2950542108 doi "https://doi.org/10.1055/s-0034-1379636" @default.
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