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Synthesis and reactivity of new l‐(1‐adamantyl)pyrazoles
Author(s) -
Cabildo P.,
Claramunt R. M.,
Elguero J.
Publication year - 1984
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570210149
Subject(s) - chemistry , reactivity (psychology) , nitration , electrophile , nucleophile , halogenation , organic chemistry , medicinal chemistry , computational chemistry , catalysis , medicine , alternative medicine , pathology
Using 1‐adamantylhydrazine as starting material, a series of 1‐(1‐adamantyl)pyrazoles has been prepared. Electrophilic reactivity (bromination and nitration) and nucleophilic reactivity (quaternarization) have been studied. Proton nuclear magnetic resonance spectra of all the new compounds are recorded.

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