An Efficient Synthesis and Selective Reaction of N-Substituted Isothiazolidinium Salts
Takeaki Naito, Okiko Miyata, Sachiko Yamakawa, Kanami Muroya
Abstract
Takeaki Naito, Okiko Miyata, Sachiko Yamakawa, Kanami Muroya
Abstract
The fust example of the preparation of N-acylated isothiazolidinium salts is described, and the sta.bility and reactivity of the isothiazolidinium salts are found to be highly dependent upon the substituent at the nitrogen atom.Dehydromethionine (I)]-3 having an isothiazolidinium structure was prepared by oxidative cyclization of an amino acid, methionine, and has been received considerable attention because of its important physiological
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The fust example of the preparation of N-acylated isothiazolidinium salts is described, and the sta.bility and reactivity of the isothiazolidinium salts are found to be highly dependent upon the substituent at the nitrogen atom.Dehydromethionine (I)]-3 having an isothiazolidinium structure was prepared by oxidative cyclization of an amino acid, methionine, and has been received considerable attention because of its important physiological
Key concepts: Chemistry, Substituent, Nitrogen atom, Reactivity (psychology), Methionine, Oxidative phosphorylation, Nitrogen, Organic chemistry