Producción Científica Profesorado

Facile synthesis of 1,3,6-oxadiazepines from 2,2?-(1,2-ethanediyldiimino)bisphenols



Rojas Lima, Susana

2001

Ma. Eugenia Ochoa Becerra, Susana Rojas-Lima, Herbert Höpfl, Patricia Rodríguez, Dolores Castillo, Rosa Luisa Santillán Baca and José Norberto Farfán García. "Facile synthesis of 1,3,6-oxadiazepines from 2,2'-(1,2-ethanediyldiimino)bisfenols. Tetrahedron, 57, 55-64 (2001). DOI: http://dx.doi.org/10.1016/S0040-4020(00)00984-4


Abstract


A useful sequence of reactions for the syntheses of a variety of heterocyclic systems including an oxadiazepine ring is described. The key step involves the condensation of substituted 2,2?-(1,2-ethanediyldiimino)bisphenols with ethanedial to provide stereoselectively the 6a,7a-trans-6,6a,7a,8,15,16-hexahydro[1,4]benzoxazine[4?,3?:6,7][1,3,6]oxadiazepino[2,3-c][1,4]-benzoxazine-6,8-diol framework, as established by X-ray diffraction analyses.



Producto de Investigación




Artículos relacionados

Facile synthesis of 1,3,6-oxadiazepines from 2,2?-(1,2-ethanediyldiimino)bisphenols

Preparation of N-aryl-substituted spiro-?-lactams via Staudinger cycloaddition

Diastereomeric C-glycosyloxanthrones from picramnia antidesma

Et3B, an Efficient Mediator for Xanthate Transfer Based Radical Processes

Synthesis and Structures of some Lithium and Sodium (Aminoalcoholato)hydrido Aluminates

Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.

New boronates prepared from 2,4-pentanedione derived ligands of the NO2 and N2O2 type comparison to...

A flexible access to highly functionalised boronates

Stereoselective addition of allylmagnesium chloride to the CN bond of [4.3.0] boron heterobicycles

Diastereoselective alkylation of chiral glycinate derivatives containing the ?-phenylethyl group.