Paper
Thermolysis of 1-(methylideneamino)-1H-pyrrole-2,3-diones. Formation of pyrazolodioxazines at [4+2]-cycloaddition of azomethinimines to arylcarbaldehydes
Published Jul 1, 2017 · V. Zhulanov, M. V. Dmitriev, A. N. Maslivets
Russian Journal of Organic Chemistry
Q4 SJR score
2
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0
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Abstract
Abstract4-Acyl-1-[(diphenylmethylidene)amino]-5-methoxycarbonyl-1Н-pyrrole-2,3-diones generate at the thermolysis 4-acyl-3-(methoxycarbonyl)-1-(diphenylmethylidene)-1H-pyrazol-1-ium-5-olates that react with aromatic aldehydes to form methyl 2-aryl-8-acyl-4,4-diphenyl-4H-pyrazolo[5,1-d][1,3,5]dioxazine-7-carboxylates whose structure is proved by X-ray diffraction analysis.
Study Snapshot
Thermolysis of 1-(methylideneamino)-1H-pyrrole-2,3-diones leads to the formation of pyrazolodioxazines, which react with aromatic aldehydes to form methyl 2-aryl-8-acyl-4,
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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