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- W2619699992 abstract "Both experimental and computational studies for the cycloaddition reaction between N-(3-pyridyl)aldimines and acetylenes where 1,5-naphthyridines are obtained are reported. The reaction of benzaldimine with a methoxycarbonyl group in position 2 with phenyl acetylene, styrene, and indene afforded polycyclic isoindolone derivatives. The mechanism of reaction of N-(3-pyridyl)aldimines with olefins can be explained by an asynchronous [4+2] cycloaddition; in the case of acetylenes, the obtained results suggest a stepwise mechanism through a 3-azatriene." @default.
- W2619699992 created "2017-06-05" @default.
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- W2619699992 date "2017-06-05" @default.
- W2619699992 modified "2023-09-25" @default.
- W2619699992 title "Study of the Hetero-[4+2]-Cycloaddition Reaction of Aldimines and Alkynes. Synthesis of 1,5-Naphthyridine and Isoindolone Derivatives" @default.
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- W2619699992 doi "https://doi.org/10.1021/acs.joc.7b00977" @default.
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