Regioselective construction of cyclohexene derivatives by Diels–Alder reactions of nitro-olefins with dienes and subsequent denitration with tributyltin hydride

Abstract
The nitro-group in the Diels–Alder adducts of nitro-olefins with dienes is replaced by hydrogen on treatment with tributyltin hydride, which offers a new method for the regioselective construction of cyclohexene derivatives.

This publication has 0 references indexed in Scilit: