Date of Award
6-1965
Document Type
Open Access
Degree Name
Bachelor of Science
Department
Chemistry
Language
English
Abstract
It had been found that 3-mercaptopropanoic acid would react readily with ammonia or primary amines yielding Schiff bases which when reacted aryl aldehydes would give 2 and 2,3 disubstituted 4-metathiazanones. The report included a variety of substituted benzaldehydes, pyridyl and thienyl carboxaldehydes, ammonia, and alkyl and aralkylamines.
Recommended Citation
Wilson, John Charles, "The Preparation of 2-Aryl-3-Methyl-4-Metathiazanones and 2-Aryl-3-Methyl-4-Thiazolidones" (1965). Honors Theses. 2130.
https://digitalworks.union.edu/theses/2130
Rights Statement
