Paquette, Leo A. published the artcileSynthesis of optically active triazolinediones and examination of their utility for inducing asymmetry in Diels-Alder cycloaddition reactions, Application In Synthesis of 2944-47-0, the publication is Journal of Organic Chemistry (1980), 45(25), 5105-13, database is CAplus.
Optically active triazolinedione derivatives of (-)-PhCHMeNH2, (+)-dehydroabietylamine acetate, and (+)-camphor, I–III, resp., were prepared and their ability to discriminate between diastereomeric transition states in their Diels-Alder reactions with racemic and optically active p-mentha-2,4-diene and α-phellandrene was studied. In each case plotting the [α]D of the adduct from the diene of known optical purity and that of the adduct from the racemic dienes vs. diastereomeric purity served to delineate the enantioselectivity and the absolute configuration of the adducts. The triazolinedione derivatives are also useful for nondestructive resolution of compounds
Journal of Organic Chemistry published new progress about 2944-47-0. 2944-47-0 belongs to ethers-buliding-blocks, auxiliary class Benzene,Ether, name is 2-Isopropylanisole, and the molecular formula is C10H14O, Application In Synthesis of 2944-47-0.
Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem