Cyclization of 1,5-hexadien-3-ols: obtention of chloro-octalines, octalones and hexahydro-azulenones from allyl-pulegols

@inproceedings{Idrissi1989CyclizationO1,
  title={Cyclization of 1,5-hexadien-3-ols: obtention of chloro-octalines, octalones and hexahydro-azulenones from allyl-pulegols},
  author={Mostafa El Idrissi and Maurice Santelli},
  year={1989}
}
Abstract The TiCl 4 mediated cyclization of allyl-pulegols gives chlorooctalines (1,5-hexadien-3-ol system is cyclized into 4-chlorocyclohexene moiety). From chloro-octalines, octalones and hexahydro-azulenones are obtained respectively into three and two steps.