Electric Literature of 79060-88-1, Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction. 79060-88-1, Name is Sodium tetrakis(3,5-bis(trifluoromethyl)phenyl)borate, SMILES is FC(C1=CC(C(F)(F)F)=CC([B-](C2=CC(C(F)(F)F)=CC(C(F)(F)F)=C2)(C3=CC(C(F)(F)F)=CC(C(F)(F)F)=C3)C4=CC(C(F)(F)F)=CC(C(F)(F)F)=C4)=C1)(F)F.[Na+], molecular formula is C32H12BF24Na, belongs to thiomorpholine compound. In a article, author is Bagnoli, Luana, introduce new discover of the category.
The reactions of readily available vinyl selenones with enantiopure 1,2-diols, N-protected-1,2-amino-alcohols, and diamines gave substituted enantiopure 1,4-dioxanes, morpholines, and piperazines, respectively, in good to excellent yields. The same procedure was extended to the synthesis of thiomorpholine, benzodiazepine, and benzoxazepine. The reactions proceeded in one pot, in the presence of base, through a simple and novel application of the Michael-initiated, ring-closure (MIRC) reactions. The formed heterocycles constitute a framework that is observed in a large number of pharmaceutical compounds.
Future efforts will undeniably focus on the diversification of the new catalytic transformations. These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. 79060-88-1, you can contact me at any time and look forward to more communication. Electric Literature of 79060-88-1.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem