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- W2951298980 abstract "The isonitriles (I) (prepared by exposure of the corresponding enones to LiCH2NC followed by TBS-Cl treatment) undergo acylation and AgBF4-promoted ring closure to give the acylpyrrolines (III) (during work-up, partial conversion of the Δ1-pyrroline (IIIa) to its Δ2-isomer (ratio 1:1.6) is observed)." @default.
- W2951298980 created "2019-06-27" @default.
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- W2951298980 date "1987-06-02" @default.
- W2951298980 modified "2023-09-27" @default.
- W2951298980 title "ChemInform Abstract: Acylnitrilium Ion Cyclizations in Heterocycle Synthesis. A Convergent Method for the Preparation of 2-Acylpyrrolines via the Intramolecular Acylation of Silyloxyalkenes with α-Keto Imidoyl Chlorides." @default.
- W2951298980 cites W2004772483 @default.
- W2951298980 doi "https://doi.org/10.1002/chin.198722099" @default.
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