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• W4323805854 endingPage "1894" @default.
• W4323805854 startingPage "1889" @default.
• W4323805854 abstract "Alkynyl hydrazones are synthesized conveniently from 2-oxo-3-butynoates and hydrazine by suppressing the susceptible formation of pyrazoles. The resultant hydrazones are transformed into alkynyl diazoacetates under metal-free and mild oxidative conditions in excellent yields. Further, the alkynyl cyclopropane and propargyl silane carboxylates are synthesized in good yields by developing an unprecedented copper-catalyzed alkynyl carbene transfer reaction." @default.
• W4323805854 created "2023-03-11" @default.
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• W4323805854 date "2023-03-10" @default.
• W4323805854 modified "2023-10-14" @default.
• W4323805854 title "Synthesis of Alkynyl Hydrazones from Unprotected Hydrazine and Their Reactivity as Diazo Precursors" @default.
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• W4323805854 doi "https://doi.org/10.1021/acs.orglett.3c00404" @default.
• W4323805854 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36897650" @default.
• W4323805854 hasPublicationYear "2023" @default.
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