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- W2065897600 abstract "Pummerer chemistry applied to 2-sulfinyl indoles promotes oxidative cyclization of pendant nucleophiles to furnish C(3) spirocyclic indolenine products. Use of tetrasubstituted silyl enol ether nucleophiles in this transform yields spirocycles featuring vicinal all-carbon quaternary centers in two cases, but fails when a nearby amine can intervene." @default.
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- W2065897600 date "2009-04-01" @default.
- W2065897600 modified "2023-09-25" @default.
- W2065897600 title "Extending Pummerer reaction chemistry. Examination of the prospects for forming vicinal quaternary carbon centers" @default.
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- W2065897600 doi "https://doi.org/10.1016/j.tetlet.2009.02.024" @default.
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