1.
Org Biomol Chem
; 17(2): 244-247, 2019 01 02.
Artículo
en Inglés
| MEDLINE
| ID: mdl-30539953
RESUMEN
A cross 1,3-dipolar cycloaddition of two different ylides between C,N-cyclic azomethine imines with an in situ-generated nonstabilized azomethine ylide from an N-benzyl precursor was realized. The reactions afforded a clean and facile access to diverse fused tricyclic 1,2,4-hexahydrotriazines in high yields (up to 96%). The chemical structures of the typical compounds were confirmed by X-ray single-crystal structure analysis.