Extended knowledge of 398489-26-4

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 398489-26-4. Safety of tert-Butyl 3-oxoazetidine-1-carboxylate.

New Advances in Chemical Research in 2021. Safety of tert-Butyl 3-oxoazetidine-1-carboxylate, You could be based in a university, combining chemical research with teaching; in a pharmaceutical company, working on developing and trialing new drugs; helping to ensure national healthcare provision keeps pace with new discoveries. 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.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 398489-26-4. Safety of tert-Butyl 3-oxoazetidine-1-carboxylate.

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