The Absolute Best Science Experiment for 398489-26-4

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 398489-26-4. Application In Synthesis of tert-Butyl 3-oxoazetidine-1-carboxylate.

Application In Synthesis of tert-Butyl 3-oxoazetidine-1-carboxylate, Academic researchers, R&D teams, teachers, students, policy makers and the media all rely on us to share knowledge that is reliable, accurate and cutting-edge. 398489-26-4, Name is tert-Butyl 3-oxoazetidine-1-carboxylate, SMILES is CC(OC(=O)N1CC(=O)C1)(C)C, belongs to isothiazole compound. In a article, author is Rodina, L. L., introduce new discover of the category.

It has been established that the interaction of diazomethane with 4,5-dialkyl-substituted 3-oxo-(2H)-isothiazole 1,1-dioxides proceeds in two stages. Initially alkylation of the sulfonimide nitrogen atom and the carbonyl group oxygen atom occurs (in a ratio of similar to 3:2), then there is a regioselective cycloaddition of diazomethane at the C=C double bond with the formation of the corresponding N-methyloxoisothiazolopyrazolines and 3-methoxyisothiazolopyrazolines.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 398489-26-4. Application In Synthesis of tert-Butyl 3-oxoazetidine-1-carboxylate.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com