Cycloaddition of methyl 2-(2,6-dichorophenyl)-2H-azirine-3-carboxylate to electron rich 2-azadienes

doi:10.1016/S0040-4039(03)01138-9

Paper

Cycloaddition of methyl 2-(2,6-dichorophenyl)-2H-azirine-3-carboxylate to electron rich 2-azadienes

Published Jun 30, 2003 · M. Alves, M. Duraes, A. Gil Fortes

Tetrahedron Letters

Q3 SJR score

20

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Abstract

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Study Snapshot

This study demonstrates that Diels-Alder cycloadducts can be formed from methyl-2H-azirine-3-carboxylate, leading to functionalized aziridines and aziridines in moderate yields.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Cycloaddition of methyl 2-(2,6-dichorophenyl)-2H-azirine-3-carboxylate to electron rich 2-azadienes

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