Synthesis of amphibean indolizidine alkaloids and related compounds from enaminone precursors

DSpace/Manakin Repository

Show simple item record

dc.contributor.author Riley, Darren Lyall
dc.date.accessioned 2008-06-20T09:11:57Z
dc.date.available 2008-06-20T09:11:57Z
dc.date.issued 2008-06-20T09:11:57Z
dc.identifier.uri http://hdl.handle.net/10539/4967
dc.description.abstract The work discussed in this thesis is centered on the synthetic protocol developed for the synthesis of alkaloids in the organic chemistry laboratories at the University of the Witwatersrand. The alkaloids of interest in this thesis are the 5,8-disubstituted indolizidines (-)-209I [185] and (-)-223V [174], the piperidine alkaloid (±)-thalictroidine [257] as well as several 5-monosubstituted indolizidines including (±)-tashiromine [330a] and (±)-5-epitashiromine [330b]. The work is put into perspective in two parts. The first part is a review of all the classes of alkaloids that have currently been isolated and identified from the skin extracts of amphibians, in particular the Dendrobatidae family of neotropical frogs. The second part gives a chronological review of all previous racemic and enantioselective syntheses of the 5,8-disubstituted indolizidines. This is followed by an overview of the general synthetic approach used in the syntheses of alkaloids in the “Wits” laboratories. Particular emphasis is placed on the enantioselective synthetic strategies, developed by Gravestock, for the synthesis of 5,8-disubstituted indolizidine alkaloids. The aims and strategies to be used in the present project are then introduced. The racemic synthesis of (±)-thalictroidine [257], used in model studies in order to practice fundamental functional group transformations for the preparation of piperidine systems is reported. The key reactions introduced in this section were the preparation of bromoacetamides, thiolactams and enaminones, the latter by the application of Eschenmoser’s sulfide contraction, as well as the reduction of exocyclic carbon-carbon double bonds in six membered vinylogous urethanes. The synthesis of (±)-thalictroidine [257], is the first reported synthesis of the natural product, and spectroscopic and crystallographic data are in agreement with the structure proposed by Kennelly et al.125 The synthesis of several 5-monosubstituted indolizidines, used in model studies in order to establish fundamental skeletal and functional group transformations for 5,8-disubstituted indolizidines are then shown. Key reactions include the preparation of several enaminones including a vinylogous urethane [312] and a Weinreb amide [314] from thiolactam [304]. These enaminones were cyclised under alkylative conditions to afford 5-substituted indolizidines [320] and [322] respectively. The synthetic utility of the Weinreb amide for the introduction of unbranched alkyl substituents at the 5-position is introduced, and the utility of the vinylogous urethane [320] is shown by a three step conversion into (±)-tashiromine [330a] and (±)-5-epi-tashiromine [330b]. The formal enantioselective synthesis of indolizidine (-)-209I [185] is reported. In order to begin the enantioselective synthesis of (-)-209I [185], methodology developed by Gravestock was adapted to the preparation and utilization of vinylogous ureas containing the Weinreb amide functionality. Conjugate addition of the secondary amine N-benzyl-N-(1R)-1- phenylethylamine [243] to tert-butyl (2E)-2-hexenoate [267] gave optically pure tertiary amine [268]. Debenzylation of this amine gave primary amine [336]. Subsequent lactam formation, thionation and sulfide contraction with N-methoxy-N-methyl-2-bromoacetamide [271] yielded vinylogous urea [272]. The reduction of tert-butyl ester [272] to liberate alcohol [273] was low yielding and an alternative method was used, which involved the reduction of the tert-butyl ester at an early stage of the synthesis, protecting it as a silyl ether, and then liberating the free alcohol at an appropriate stage in the synthesis. The silyl ether was not compatible with the thionation step and was swapped at the lactam stage for an acetate protecting group. Subsequent reactions included an acylative cyclisation to form the indolizidine skeleton and a stereoselective reduction of the carbon-carbon double bond to yield (5R,8S,8aS)-N-methoxy-N-methyl-5-propyloctahydro-8-indolizinecarboxamide [275]. Mono-alkylation of the Weinreb amide functionality and epimerization to 1-[(5R,8R,8aS)-5- propyloctahydro-8-indolizinyl]-1-propanone [191] represented a formal synthesis of indolizidine (-)-209I [185]. Approaches towards the synthesis of a late stage common intermediate [259] which could have the substituents at both the 5- and 8-positions modified independent of each other at or near the end of the synthesis are discussed. Finally an alternative synthetic approach negating the need for several of the protection and deprotection steps is shown with regards to the synthesis of the structurally related 1,4-disubstituted quinolizidines en
dc.format.extent 2544500 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.title Synthesis of amphibean indolizidine alkaloids and related compounds from enaminone precursors en
dc.type Thesis en


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search WIReDSpace


Browse

My Account

Statistics