Bibliografías temáticas / Olefination

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Literatura académica sobre el tema "Olefination"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 25 de abril de 2022

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Tesis sobre el tema "Olefination"

1

Blakemore, Paul Richard. "Development and application of the one-pot Julia olefination." Thesis, University of Glasgow, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.284730.

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2

Pedro, Filipe Miguel Esteves. "Application of rhenium and ruthenium organometallic complexes in carbonyl olefination." [S.l.] : [s.n.], 2007. http://mediatum2.ub.tum.de/doc/618877/document.pdf.

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Smith, Nicholas David. "A total synthesis of herboxidiene A." Thesis, University of Southampton, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242395.

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4

Strand, Daniel. "Methods for Asymmetric Olefination Reactions; Development and Application to Natural Product Synthesis." Doctoral thesis, Stockholm : Chemical Science and Engineering, KTH, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4088.

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5

Middleditch, Michael. "Towards a catalytic carbonyl olefination reaction using metal oxo complexes and ketenes." Thesis, University of Nottingham, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.430565.

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6

Gold, J. B. "Development of a dithiane-Julia olefination reaction : towards the synthesis of callipeltoside A." Thesis, University of Cambridge, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.599468.

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This doctoral thesis is divided into three sections: Part A, Part B and Part C. Part A is subdivided further into three chapters. In the first of these, an overview of the Julia olefination reaction process as well as its variants is provided, followed by a short description of the application of dithiane methodology in natural product synthesis. The second chapter describes the development of a new methodology based on Julia olefination of substrates derived from dithiane and dithiolane sulfones. Summary and conclusions then follow in chapter three. Part B of this thesis is also subdivided in
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7

Sun, Xiang Verfasser], Tobias [Akademischer Betreuer] Ritter, and Carsten [Akademischer Betreuer] [Bolm. "Decarboxylative functionalization: catalytic olefination and polyfluoroarylation of alkylcarboxylic acids / Xiang Sun ; Tobias Ritter, Carsten Bolm." Aachen : Universitätsbibliothek der RWTH Aachen, 2021. http://d-nb.info/1240390920/34.

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8

Niwetmarin, Worawat. "(-)-Cytisine : an entry to a multipoint chiral scaffold : Zweifel olefination towards functionalised alkenes and C-glycals." Thesis, University of Bristol, 2017. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730848.

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9

Bedore, Matthew William. "Synthesis of Key Fragments Contained in the Framework of Amphidinol 3." The Ohio State University, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=osu1211485773.

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10

Shuter, Emily Clare. "Studies toward the synthesis of the microsclerodermin natural products." Faculty of Science, School of Chemistry, University of Sydney, 2006. http://hdl.handle.net/2123/1970.

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Doctor of Philosophy (PhD), Science<br>A concise stereo-selective synthesis of a protected form of APTO 1, an unusual amino acid component of microsclerodermin C 2, was undertaken. Sequential Sharpless Asymmetric Aminohydroxylation (AA) and Asymmetric Dihydroxylation (AD) reactions were used to introduce the chiral amino and hydroxyl groups. Specific directing groups were chosen to ensure high regio- and enantio-selectivity in these reactions. The target compound was reached in a linear reaction sequence of fourteen steps. The strategy was designed to generate common intermediates which cou
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