RESUMO

We describe a protocol developed for the preparation of ß-enaminoketones derived from 1,3-cyclohexanediones, and their subsequent reduction by sodium in THF-isopropyl alcohol to afford cis- and trans-3-aminocyclohexanols.

Assuntos

Cicloexanóis/síntese química , Cetonas/química , Cicloexanóis/química , Modelos Moleculares , Oxirredução , Estereoisomerismo