No abstract

No abstract

No abstract

The four possible isomers of benz [o]anthracene containing a cyclopenta-fused ring have been synthesized and characterized. These systems are of interest for structure-activity studies in bioactivation because of their predicted high level of activity. Formation of fused five-membered rings by intramolecular cyclodehydration, often difficult to accomplish, was found to be smoothly effected in anhydrous HF, provided the reactivity index (Nt) for the appropriate electrophilic addition was favorable. The dihydro polycyclic aromatic alcohols obtained from reduction of the corresponding keto cyclodehydration products were best dehydrated to the desired PAH by activity grade I neutral alumina in refluxing benzene. This dehydration proceeds in high yield without the formation of isomeric or polymeric side products that occurred even under such mild acid catalysis as p-toluenesulfonic acid.Recent confirmation of the mutagenicity and carcinogenicity of cyclopentatcdjpyrene1 (CPP, 1) and development of screening systems based on structure-activity