Paper
Synthesis of methyl 2-[(benzyloxycarbonyl)amino]-3-cyanopropenoate and its transformations into derivatives of pyrrole, 2,5-dioxoimidazolidine, 1H-pyrazole, and 4,6-diaminopyridazine
Published May 1, 2006 · B. Stanovnik, Uroš Uršič, D. Bevk
Heterocycles
Q4 SJR score
3
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0
Influential Citations
Abstract
Methyl (E)-2-[(benzyloxycarbonyl)amino]-3-cyanopropenoate (4) was, as a versatile multifunctional reagent, transformed with hydrazine and monosubstituted aromatic and heteroaromatic hydrazines under various conditions into derivatives of pyridazine (6), pyrrole (7), imidazole-2,4-dione (9), and pyrazole (13).
Study Snapshot
Methyl 2-[(benzyloxycarbonyl)amino]-3-cyanopropenoate can be transformed into pyrrole, 2,5-dioxoimidazolidine, 1H-pyrazole, and 4,6-diaminopyrida
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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