An Enantioselective Approach Towards the Synthesis of 3-Aryl Substituted Piperidines: Application to (-)-Preclamol Synthesis

dc.contributor.authorSharma, Pooja
dc.contributor.supervisorPrakash, Ranjana
dc.contributor.supervisorPandey, Satyendra Kumar
dc.date.accessioned2017-08-08T11:14:44Z
dc.date.available2017-08-08T11:14:44Z
dc.date.issued2017-08-08
dc.descriptionMaster of Science -Chemistryen_US
dc.description.abstractDue to the biological activity of 3-Aryl substituted piperidines and their derivatives in organic chemistry and also their activity in the treatment of Perkinson’s, schizophreni and many other diseases.An enantioselective approach towards the development of a new synthetic route of (-)-preclamol has been attempted employing Henry reaction, asymmetric Michael addition showing the catalytic activity of TMS prolinol, DIBAL-H reduction . The merits of this approach is to provide a high yielding reaction steps. Column chromatography, NMR Spectroscopy were employed to purify and identification of these synthetic intermediates.en_US
dc.identifier.urihttp://hdl.handle.net/10266/4600
dc.language.isoenen_US
dc.subjectAryl Piperidineen_US
dc.subjectAsymmetric Michael additionen_US
dc.subjectAntipsychotic drugen_US
dc.subjectdopamine autoreceptoren_US
dc.subject3-PPPen_US
dc.titleAn Enantioselective Approach Towards the Synthesis of 3-Aryl Substituted Piperidines: Application to (-)-Preclamol Synthesisen_US
dc.typeThesisen_US

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