Never Underestimate The Influence Of Anthracene-9,10-dione

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. 84-65-1, you can contact me at any time and look forward to more communication. Electric Literature of 84-65-1.

Electric Literature of 84-65-1, Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction. 84-65-1, Name is Anthracene-9,10-dione, SMILES is O=C1C2=C(C=CC=C2)C(C3=CC=CC=C13)=O, molecular formula is C14H8O2, belongs to thiomorpholine compound. In a article, author is Vijay, Murugan, introduce new discover of the category.

Regiospecific Bi-Catalysed Domino C-N/C-S Bonds Formation: Synthesis of 1,4-Thiazines/1,4-Thiomorpholines

A domino Bi-catalysed C-N/C-S bond formation of N-sulfonylaziridines is developed with 1,4-dithiane-2,5-diol to give 3,4-dihydro-1,4-thiazines at room temperature. The use of Bi(OTf)(3) as a catalyst, atom economy and regioselectivity are the important practical features.

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. 84-65-1, you can contact me at any time and look forward to more communication. Electric Literature of 84-65-1.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem