Flexible application of in synthetic route 35836-73-8

If you want to learn more about this compound(2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol)Reference of 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(35836-73-8).

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Manganese-Mediated Direct Functionalization of Hantzsch Esters with Alkyl Iodides via an Aromatization-Dearomatization Strategy, published in 2021-05-21, which mentions a compound: 35836-73-8, mainly applied to Hantzsch ester alkyl iodide manganese catalyst alkylation; alkyl Hantzsch ester preparation, Reference of 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol.

Manganese-mediated direct functionalization of the Hantzsch esters with readily accessible alkyl iodides through an aromatization-dearomatization strategy was reported for the first time. Applying this protocol, a library of valuable 4-alkyl-1,4-dihydropyridines were facilely afforded in good yields. This simple and practical reaction proceeded under visible-light irradiation at room temperature and displays high functional-group compatibility. Addnl., the method was applicable for gram-scale synthesis and late-stage functionalization of complex mols.

If you want to learn more about this compound(2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol)Reference of 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(35836-73-8).

Reference:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics