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SYNTHESIS OF 2H-1,14.-BENZOTHIAZINES AND RELATED COMPOUNDS

dc.contributor.advisorCoutts, R.T.
dc.creatorPeel, Harold Warren
dc.date.accessioned2023-12-13T20:51:28Z
dc.date.available2023-12-13T20:51:28Z
dc.date.issued1965
dc.date.submittedOctober 1965
dc.description.abstractA variety of reasons exist for making an invest-igation into the chemistry of cyclic hydroxamic acids, especially% those possessing a 2H-1,4-benzothiazine nucleus. These reasons are discussed below. Cyclic hydroxamic acids, as the name suggests, possess a hydroxamate group which exists in an equilibrium between the two forms, as shown (I). The group is strongly acidic in natures being sol-uble in relatively weak bases such as sodium bicarbonate. The hydroxamic acid group is able to form chelates with metals. The structure of a divalent metal chelate is thought to be as shown (II)
dc.identifier.urihttps://hdl.handle.net/10388/15350
dc.subjectCyclic hydroxamic acids
dc.titleSYNTHESIS OF 2H-1,14.-BENZOTHIAZINES AND RELATED COMPOUNDS
dc.type.genreThesis
thesis.degree.departmentPharmacy
thesis.degree.grantorUniversity of Saskatchewanen_US
thesis.degree.levelMasters
thesis.degree.nameMaster of Science (M.Sc.)

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