1999HeterocyclesOpen access

An Efficient Synthesis and Selective Reaction of N-Substituted Isothiazolidinium Salts

Takeaki Naito, Okiko Miyata, Sachiko Yamakawa, Kanami Muroya

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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

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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

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Available 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

Key concepts: Chemistry, Substituent, Nitrogen atom, Reactivity (psychology), Methionine, Oxidative phosphorylation, Nitrogen, Organic chemistry

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