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- W4244080223 abstract "Vinyldiazo compounds undergo a thermal electrocyclization to form pyrazoles in yields of up to 95%. The reactions are operationally simple, use readily available starting materials, require no intervention of a catalyst, and enable the synthesis of mono-, di- and tri-substituted pyrazoles. With the ability to produce highly substituted pyrazole and the flexibility in installing various types of substituents, this method constitutes a new entry to this valuable heterocyclic scaffold of interest in all branches of chemical industry." @default.
- W4244080223 created "2022-05-12" @default.
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- W4244080223 date "2020-03-19" @default.
- W4244080223 modified "2023-09-24" @default.
- W4244080223 title "Intramolecular Cyclization of Vinyldiazoacetates as a Versatile Route to Substituted Pyrazoles" @default.
- W4244080223 doi "https://doi.org/10.26434/chemrxiv.11996655" @default.
- W4244080223 hasPublicationYear "2020" @default.
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