Metal-free Synthesis of Trisubstituted Pyrazoles by the Reaction Between Hydrazones and Activated Olefins

dc.contributor.authorBhaskaran, R.P.
dc.contributor.authorSreelekha, M.K.
dc.contributor.authorBabu, B.P.
dc.date.accessioned2026-02-04T12:27:30Z
dc.date.issued2022
dc.description.abstractThe reactivity of various activated olefins towards the [3+2] annulation with hydrazones (aza-enamines) has been studied. Nitroolefins, methyl vinyl ketone, acrylates and acrylamide were found to react with aldehyde hydrazones of different electronic nature to generate 1,3,5-/1,3,4–trisubstituted pyrazoles selectively. A detailed optimization study was conducted to derive the best condition for the annulation reaction of different olefin partner and the intermediate dihydropyrazole is also identified. © 2022 Wiley-VCH GmbH.
dc.identifier.citationChemistrySelect, 2022, 7, 44, pp. -
dc.identifier.urihttps://doi.org/10.1002/slct.202202773
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/22314
dc.publisherJohn Wiley and Sons Inc
dc.subjectAcrylate
dc.subjectHydrazone
dc.subjectMethyl vinyl ketone
dc.subjectNitroolefin
dc.subjectPyrazole
dc.subject[3+2] annulation
dc.titleMetal-free Synthesis of Trisubstituted Pyrazoles by the Reaction Between Hydrazones and Activated Olefins

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