So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Vyglazov, O. G.; Urbanovich, T. R.; Manukov, E. N.; Chuiko, V. A.; Udarov, B. G. researched the compound: 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol( cas:35836-73-8 ).Name: 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol.They published the article 《Solvolysis products of 2-[(tosyloxy)ethyl]-6,6-dimethylbicyclo[3.1.1]hept-2-ene》 about this compound( cas:35836-73-8 ) in Zhurnal Organicheskoi Khimii. Keywords: acetolysis tosyloxyethyldimethyl bicycloheptene. We’ll tell you more about this compound (cas:35836-73-8).
Acetolysis of the title tosylate gave a mixture of aromatic and bi- and tricyclic products, with alcs. I and II predominating, in 79% combined yield. Oxidizing β-pinene with Pb(OAc)4 in C6H6 gave 78% trans-3-acetoxy-2(10)-pinene, which was cyclopropanated with :CCl2 to give 88% dichlorospiro ester and then reduced with LiAlH4 in dioxane to give 73% I.
In addition to the literature in the link below, there is a lot of literature about this compound(2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol)Name: 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol, illustrating the importance and wide applicability of this compound(35836-73-8).
Reference:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics