Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Monatshefte fuer Chemie called CAN-based oxidative annulation of alkenols with 1,3-dicarbonyl compounds, Author is Ciez, Dariusz; Koziel, Krzysztof; Horvath, Branislav; Svetlik, Jan, which mentions a compound: 35836-73-8, SMILESS is CC1(C)[C@@]2([H])CC=C(CCO)[C@]1([H])C2, Molecular C11H18O, Recommanded Product: 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol.
A mild protocol for the reaction of 1,3-dicarbonyl compounds with a range of alkenols mediated by CAN was described. The oxidative free radical cyclization leading to corresponding dihydrofuran derivatives tolerated the presence of hydroxyl group.
The article 《CAN-based oxidative annulation of alkenols with 1,3-dicarbonyl compounds》 also mentions many details about this compound(35836-73-8)Recommanded Product: 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol, you can pay attention to it, because details determine success or failure
Reference:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics