Relevant bibliographies by topics / Alkaloid synthesis; Indole alkaloids

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Academic literature on the topic 'Alkaloid synthesis; Indole alkaloids'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Dissertations / Theses on the topic "Alkaloid synthesis; Indole alkaloids"

1

Callaghan, Owen. "Synthetic and mechanistic studies in free radical." Thesis, University of Strathclyde, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366957.

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2

Hollinshead, S. P. "Enantiospecific approaches to indole alkaloids." Thesis, University of York, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379030.

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3

Swain, D. J. "Stereoselective synthesis of indole alkaloids." Thesis, University of Oxford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238115.

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4

Wingfield, M. "A novel approach to the total synthesis of corynanthe indole alkaloids via cyclopentanoid intermediaries." Thesis, University of Manchester, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.374789.

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5

McLay, Neil Robert. "The synthesis of bridged indole alkaloids." Thesis, University of York, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.280410.

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6

Hilton, Stephen. "Towards the synthesis of indole alkaloids." Thesis, Kingston University, 2002. http://eprints.kingston.ac.uk/20698/.

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Radical chemistry and, in particular, tandem radical chemistry has rarely been used in the synthesis of the 'Strychnos' and 'Aspidosperma' alkaloids. These two classes of compounds are structurally complex, possess a range of biological activity and present a synthetic challenge. Previous routes to these molecules are reviewed in the first section . of this thesis. The utility of radical chemistry, tandem radical chemistry and 1,S'I hydrogen atom abstraction towards the syntheses of complex molecules is outlined with examples that demonstrate the potential of radical chemistry. A new synthetic
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7

Ouali, Dehimi. "Enantioselective synthesis of novel corynanthe indole alkaloid synthons." Thesis, University of Salford, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315329.

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8

Cheung, Man-ki. "Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole /." [Hong Kong] : University of Hong Kong, 1995. http://sunzi.lib.hku.hk/hkuto/record.jsp?B14786898.

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9

張文驥 and Man-ki Cheung. "Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1995. http://hub.hku.hk/bib/B31234148.

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10

Ferreira, Jasmin. "Asymmetric Total Synthesis of the Pentacyclic Indole Alkaloid (+)-Tacamonine." Master's thesis, Faculty of Science, 2019. http://hdl.handle.net/11427/31346.

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(+)-Tacamonine, a natural product isolated from the Central African plant Tabernaemontana eglandulosa, belongs to the relatively new tacaman class of pentacyclic monoterpenoid indole alkaloids. Its close structural similarity to the potent cerebral vasodilator (-)-vincamone has promoted several efforts towards its synthesis, culminating in the appearance of two asymmetric and seven racemic syntheses in the literature. This dissertation details the successful execution of our strategy for the concise, highly-efficient, asymmetric total synthesis of (+)-tacamonine. Chapter 1 serves as an introdu
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