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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/13624
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dc.contributor.advisorWarkentin, J.en_US
dc.contributor.authorRamakrishnan, Kottiethen_US
dc.date.accessioned2014-06-18T17:04:39Z-
dc.date.available2014-06-18T17:04:39Z-
dc.date.created2009-08-21en_US
dc.date.issued1975-12en_US
dc.identifier.otheropendissertations/846en_US
dc.identifier.other1752en_US
dc.identifier.other962098en_US
dc.identifier.urihttp://hdl.handle.net/11375/13624-
dc.description.abstract<p>Several new oxadiazolines have been synthesized by the cyclization of mixed carbohydrazones derived from aromatic aldehydes and aliphatic ketones. A mechanism for the cyclization is discussed on the basis of the regiospecificity observed in these reactions. Pyrolysis of these oxadiazolines led to the synthesis of a number of azomethine imine ylids, which could not be made by the only other existing route. The mechanism of this pyrolytic process was investigated by trapping experiments and spectroscopic methods and the intermediacy of an N-isocyanatoimine was established. Structures of the products formed by the trapping experiments were also determined.</p>en_US
dc.subjectChemistryen_US
dc.subjectChemistryen_US
dc.titleSynthetic and Mechanistic Studies Related to Oxadiazolines and Azomethine Imine Ylidsen_US
dc.typethesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
Appears in Collections:Open Access Dissertations and Theses

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