Domino ‘Staudinger–aza-Wittig–1,5-phosphonium-rearrangement–fragmentation’ reactions of 1-azido-2-hydroxy-4,6-dioxohexanes
Literature Information
Peter Langer, Heydar Shojaei
The domino ‘Staudinger–aza-Wittig–1,5-phosphonium-rearrangement–fragmentation’ reaction of 1-azido-2-hydroxy-4,6-dioxohexanes allows a convenient synthesis of functionalized 1-acetamido-2-alkylidenecyclopentanes.
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![5,10-Dihydroindeno[2,1-a]indene structure 5,10-Dihydroindeno[2,1-a]indene structure](https://static.chemtradehub.com/structs/654/6543-29-9-71ca.webp)
![Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure](https://static.chemtradehub.com/structs/102/1020719-57-6-37e2.webp)

