Synthetic approach towards methyllycaconitine

dc.contributor.advisor George A. Kraus
dc.contributor.author Kesavan, Sarathy
dc.contributor.department Chemistry
dc.date 2018-08-25T04:45:33.000
dc.date.accessioned 2020-06-30T07:15:21Z
dc.date.available 2020-06-30T07:15:21Z
dc.date.copyright Thu Jan 01 00:00:00 UTC 2004
dc.date.issued 2004-01-01
dc.description.abstract <p>Organic synthesis, with the invention of new synthetic strategies and technologies, has evolved from largely empirical approaches for the preparation of relatively simple molecules to sophisticated strategies for the construction of molecules with considerable structural and functional complexity. Organic synthesis is employed to synthesize the natural product and its analogs for the discovery of new drugs. The development of new synthetic methodologies in the course of total synthesis is imperative for the efficient synthesis of drug candidates. Apart from the practical applications, the pursuit of efficient syntheses of complex natural products is both gratifying and truly enjoyable.;Chapter One describes the development of annulation reaction for the construction of five-, six- and seven-membered rings. Chapter Two describes a direct approach to the synthesis of methyllycaconitine, a representative of the aconitine alkaloids. The numbering of the compounds, schemes and references are independent in each section.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/rtd/1174/
dc.identifier.articleid 2173
dc.identifier.contextkey 6090694
dc.identifier.doi https://doi.org/10.31274/rtd-180813-10971
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath rtd/1174
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/65030
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/rtd/1174/r_3158348.pdf|||Fri Jan 14 18:57:13 UTC 2022
dc.subject.disciplines Organic Chemistry
dc.subject.keywords Chemistry
dc.subject.keywords Organic chemistry
dc.title Synthetic approach towards methyllycaconitine
dc.type article
dc.type.genre dissertation
dspace.entity.type Publication
relation.isOrgUnitOfPublication 42864f6e-7a3d-4be3-8b5a-0ae3c3830a11
thesis.degree.level dissertation
thesis.degree.name Doctor of Philosophy
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