http://10.10.120.238:8080/xmlui/handle/123456789/774| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sharma A. | en_US |
| dc.contributor.author | Jamwal P. | en_US |
| dc.contributor.author | Vaid H. | en_US |
| dc.contributor.author | Gurubrahamam R. | en_US |
| dc.date.accessioned | 2023-11-30T08:49:28Z | - |
| dc.date.available | 2023-11-30T08:49:28Z | - |
| dc.date.issued | 2023 | - |
| dc.identifier.issn | 1523-7060 | - |
| dc.identifier.other | EID(2-s2.0-85149921952) | - |
| dc.identifier.uri | https://dx.doi.org/10.1021/acs.orglett.3c00404 | - |
| dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/774 | - |
| dc.description.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. © 2023 American Chemical Society. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.source | Organic Letters | en_US |
| dc.title | Synthesis of Alkynyl Hydrazones from Unprotected Hydrazine and Their Reactivity as Diazo Precursors | en_US |
| dc.type | Journal Article | en_US |
| Appears in Collections: | Journal Article | |
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