Phosphite-thioether/selenoether Ligands from Carbohydrates: An Easily Accessible Ligand Library for the Asymmetric Hydrogenation of Functionalized and Unfunctionalized Olefins was written by Margalef, Jessica;Borras, Carlota;Alegre, Sabina;Alberico, Elisabetta;Pamies, Oscar;Dieguez, Montserrat. And the article was included in ChemCatChem in 2019.Application of 29364-29-2 This article mentions the following:
A large family of phosphite-thioether/selenoether ligands I (L1-L24; E = S, Se; R1 = Ph, naphthyl; R-R = substituted 1,1′-biphenyl-2,2′-diyl, 1,1′-binaphthalen-2,2′-diyl; R2-R4 = H or R2, R3 = Me, R4, R5 = H; R2 = R4 = Me, R3 = R5 = H or R3 = R5 = Ph, R2 = R4 = H) has been easily prepared from accessible
Sodium 2-methyl-2-propanethiolate (cas: 29364-29-2) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Application of 29364-29-2
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts