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Selective and reversible 1,3-dipolar cycloaddition of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with 1,3-diphenylprop-2-en-1-ones under microwave irradiation

The first example of the cycloaddition of in situ-generated azomethine imine under microwave conditions is described. The reaction of 6-aryl-1,5-diazabicyclo[3.1.0]hexanes with 1,3-diphenylprop-2-en-1-ones proceeds regio- and stereoselectively giving mostly good yields of the corresponding perhydrop...

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Detalles Bibliográficos
Autores principales:	Molchanov, Alexander P, Efremova, Mariia M, Kryukova, Mariya A, Kuznetsov, Mikhail A
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Beilstein-Institut 2020
Materias:	Full Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607433/ https://www.ncbi.nlm.nih.gov/pubmed/33178358 http://dx.doi.org/10.3762/bjoc.16.218

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