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- W2974728235 endingPage "15247" @default.
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- W2974728235 abstract "Abstract Cycloadditions of strained carbocycles promoted by Lewis acids are powerful methods to construct heterocyclic frameworks. In fact, the formal [3+2] cycloadditions of donor–acceptor (DA) cyclopropanes with nitriles has seen particular success in synthesis. In this work, we report on the first [4+2] cycloaddition of nitriles with DA cyclobutanes by Lewis acid activation. Tetrahydropyridine derivatives were obtained in up to 91 % yield from various aryl‐activated cyclobutane diesters and aliphatic or aromatic nitriles." @default.
- W2974728235 created "2019-09-26" @default.
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- W2974728235 date "2019-10-31" @default.
- W2974728235 modified "2023-10-11" @default.
- W2974728235 title "Synthesis of Functionalized Tetrahydropyridines by SnCl<sub>4</sub>‐Mediated [4+2] Cycloaddition between Donor–Acceptor Cyclobutanes and Nitriles" @default.
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- W2974728235 doi "https://doi.org/10.1002/chem.201903833" @default.
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