Development of New Synthetic Approaches Towards the Total Synthesis of Biologically Active Natural Products

dc.contributor.authorAnju
dc.contributor.supervisorPrakash, Ranjana
dc.contributor.supervisorPandey, Satyendra Kumar
dc.date.accessioned2022-08-22T07:26:45Z
dc.date.available2022-08-22T07:26:45Z
dc.date.issued2022-08-22
dc.description.abstractWe have developed enantioselective approaches for the synthesis of (+)-(2S,3S,5S)-epi- muscarine, (+)-nephrosteranic acid employing Sharpless AD and organocatalzyed Michael addition reactions as key steps. We have also attempted the synthesis of (-)- trachelanthamidine. The merits of these synthetic approaches are high enantio- and diastereoselectivity with high yielding reaction steps.en_US
dc.identifier.urihttp://hdl.handle.net/10266/6266
dc.language.isoenen_US
dc.subjectSharpless asymmetric dihydroxylationen_US
dc.subjectMichael addition reactionsen_US
dc.subjectepi-muscarineen_US
dc.subject(+)-nephrosteranic aciden_US
dc.subjectSwern oxidation conditionsen_US
dc.titleDevelopment of New Synthetic Approaches Towards the Total Synthesis of Biologically Active Natural Productsen_US
dc.typeThesisen_US

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