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Synthesis of Cyclic N-Sulfonylamidines through Ritter Type Reaction using Carene and Pinene Derivatives via Carbocation Rearrangement

dc.contributor.advisorChandrasekaran, S
dc.contributor.authorGanesh, V
dc.date.accessioned2018-02-11T07:08:15Z
dc.date.accessioned2018-07-30T15:14:18Z
dc.date.available2018-02-11T07:08:15Z
dc.date.available2018-07-30T15:14:18Z
dc.date.issued2007-07
dc.date.submitted2007
dc.identifier.urihttps://etd.iisc.ac.in/handle/2005/3090
dc.description.abstractThe present work mainly focuses on the reactivity of monoterpenes like Carenes, Pinenes and their derivatives, which has vinylcyclopropane or vinylcyclobutane linkage. These moieties were well known to rearrange by treating with acid, radical attack, pyrolysis, etc., to give structurally interesting compounds
dc.language.isoen_USen_US
dc.relation.ispartofseriesG25536en_US
dc.subjectOrganic Synthesisen_US
dc.subjectCyclic N-Sulfonylamidinesen_US
dc.subjectRitter Type Reactionen_US
dc.subjectCareneen_US
dc.subjectPineneen_US
dc.subjectCarbocation Rearrangementen_US
dc.subjectMonoterpenesen_US
dc.subject.classificationOrganic Chemistryen_US
dc.titleSynthesis of Cyclic N-Sulfonylamidines through Ritter Type Reaction using Carene and Pinene Derivatives via Carbocation Rearrangementen_US
dc.typeThesisen_US
dc.degree.nameMSen_US
dc.degree.levelMastersen_US
dc.degree.disciplineFaculty of Scienceen_US


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