The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol( cas:35836-73-8 ) is researched.Safety of 2-((1R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethanol.Kaminski, Z. J.; Kolesinska, B.; Markowicz, S. W.; Pokrzeptowicz, K. published the article 《Terpenic alcohols – source of chirality in condensing reagents in peptide chemistry》 about this compound( cas:35836-73-8 ) in Polish Journal of Chemistry. Keywords: terpenyloxytriazine preparation enantiodifferentiation reagent peptide coupling; triazine dichloroterpenyloxy preparation enantiodifferentiation peptide coupling. Let’s learn more about this compound (cas:35836-73-8).
Chiral 2,4-dichloro-6-terpenyloxy-1,3,5-triazines, obtained by treatment of cyanuric chloride with isomyrtanol, nopol, isopinocampheol and borneol, are useful as enantiodifferentiating coupling reagent in the synthesis of dipeptides.
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)Safety of 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