Nelson, Adam published the artcileAsymmetric dihydroxylation of allylic phosphine oxides, Category: catalysis-chemistry, the publication is Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1997), 2645-2657, database is CAplus.
Diphenylphosphinoyl diols have been produced by asym. dihydroxylation (AD) of allylic phosphine oxides and have been useful synthetic intermediates. The results of this study are discussed in terms of the model which has been proposed by Sharpless to explain the enantioselectivity of his AD reaction. Thus, Sharpless asym. dihydroxylation of (E)-1-diphenylphosphinoylbut-2-ene (preparation given) in the presence of AD-mix-¦Á/sulfonamide in alc./water gave 84% (2R,3S)-1-diphenylphosphinoylbutane-2,3-diol. The dihydroxylation results are thus of both mechanistic and synthetic value.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry published new progress about 4141-48-4. 4141-48-4 belongs to catalysis-chemistry, auxiliary class Aryl phosphine ligand,Mono-phosphine Ligands, name is Allyldiphenylphosphine oxide, and the molecular formula is C15H15OP, Category: catalysis-chemistry.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia