Can You Really Do Chemisty Experiments About (R)-[1,1′-Binaphthalene]-2,2′-diol

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 18531-94-7, help many people in the next few years.Product Details of 18531-94-7

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Product Details of 18531-94-7, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 18531-94-7, Name is (R)-[1,1′-Binaphthalene]-2,2′-diol, molecular formula is C20H14O2. In a Article, authors is Fraser, Paul K.£¬once mentioned of 18531-94-7

Highly enantioselective conjugate addition of AlMe3 to linear aliphatic enones by a designed catalyst

2-Hydroxy-2?-alkylthio-1,1?-binaphthy compounds are catalytic promoters of the 1,4-addition of AlMe3 to linear aliphatic enones in THF at -40 to -48C in the presence of [Cu(MeCN)4]BF4. At ligand loadings of 5-20 mol%, enantioselectivities of 80-93% are realised for most substrates. To attain these values, the use of highly pure AlMe3 is mandatory. The presence of methylalumoxane (MAO), derived by hydrolysis, leads to reduced enantioselectivity and a conjugate addition product.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 18531-94-7, help many people in the next few years.Product Details of 18531-94-7

Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI