Product Details of 189518-78-3On May 1, 1998 ,《A new approach to highly enantioselective polymeric chiral catalysts》 appeared in Journal of Organic Chemistry. The author of the article were Hu, Qiao-Sheng; Huang, Wei-Sheng; Pu, Lin. The article conveys some information:
A rigid, sterically regular, binaphthol-based, polymeric, chiral catalyst was prepared and used for the asym. reaction of aldehydes with Et2Zn. The ee values obtained were generally 96-98%, the polymer was easily recovered by precipitation with MeOH, and the recovered polymer showed the same enantioselectivity as the original polymer. The experimental part of the paper was very detailed, including the reaction process of (R)-3,3′-Diiodo-2,2′-bis(methoxymethoxy)-1,1′-binaphthalene(cas: 189518-78-3Product Details of 189518-78-3)
(R)-3,3′-Diiodo-2,2′-bis(methoxymethoxy)-1,1′-binaphthalene(cas: 189518-78-3) belongs to organic iodides. Generally organic iodides can be divided into two classes of alkyl iodides and aryl iodides. Typical reactions of alkyl iodides include nucleophilic substitution, elimination, reduction, and the formation of organometallics.Product Details of 189518-78-3
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com