Alame, M. published the artcile2,2′-Bis-[bis(4-substituted-phenyl)phosphino]-1,1′-binaphthyl derivatives in Rh(I)-catalyzed hydrogenation of acetamidoacrylic acid derivatives: Electronic effects, Product Details of C22H12F6O6S2, the publication is Journal of Molecular Catalysis A: Chemical (2007), 271(1-2), 18-24, database is CAplus.
Electronic effects of electron-donating and electron-withdrawing substituents at the para position of the Ph moieties of BINAP ligands were studied towards asym. hydrogenation of α-(acylamino)acrylic acids. Enantiomeric excesses varied as a linear relationship towards Hammett coefficients σp of electron-donating groups between 0 and -0.63.
Journal of Molecular Catalysis A: Chemical published new progress about 126613-06-7. 126613-06-7 belongs to esters-buliding-blocks, auxiliary class Chiral Diphenols, name is (R)-[1,1′-Binaphthalene]-2,2′-diyl bis(trifluoromethanesulfonate), and the molecular formula is C22H12F6O6S2, Product Details of C22H12F6O6S2.
Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics