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- W2952079276 abstract "An indoxyl-based strategy for the synthesis of indolines and indolenines via unprecedented aza-pinacol and aza-semipinacol rearrangements was developed. This method provides direct access to the core structures of several classes of indole alkaloids. The synthetic utility was demonstrated by the divergent synthesis of an array of functionalized polycyclic structures from a common intermediate and the formal total synthesis of the indoline natural product minfiensine. The reversed reactivity of indoxyl as a building block compared to that of indole offers a conceptually distinct disconnection strategy for indoline- and indolenine-containing heterocycles and natural products." @default.
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- W2952079276 date "2016-02-01" @default.
- W2952079276 modified "2023-09-24" @default.
- W2952079276 title "ChemInform Abstract: An Indoxyl-Based Strategy for the Synthesis of Indolines and Indolenines." @default.
- W2952079276 cites W1898999538 @default.
- W2952079276 doi "https://doi.org/10.1002/chin.201610124" @default.
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