Abstract 2-(Cyclohex-2′-enyl)-5,5-dimethyl-3-hydroxycyclohex-2-enone undergoes regioselective heterocyclization to give bridged heterocycles 5a,b and 7 on treatment with pyridine hydrotribromide or hexamethylenetetramine hydrotribromide (1 h); or elemental bromine (7 h); N-iodosuccinimide in acetonitrile at 0–5°C (1 h) and conc. H2SO4 at 0–5°C (2 h), respectively.

This study demonstrates a regioselective heterocyclization of 2-(Cyclohex-2′-enyl)-5,5-dimethyl-3-hydroxycyclohex-2-enone to give bridged heterocycles 5a,b, and 7 using pyridine hydrotrib

Paper

Synthesis of Dimedone-Annelated Heterocycles: Regioselective Heterocyclization of 2-(Cyclohex-2′-enyl)-5,5-dimethyl-3-hydroxy cyclohex-2-enone

References

Citations