Academic literature on the topic 'Alkane And Alkene'

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Dissertations / Theses on the topic "Alkane And Alkene"

1

Peter, Sebastian. "Oxyfunctionalization of alkanes, alkenes and alkynes by unspecific peroxygenase (EC 1.11.2.1)." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-113321.

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Unspecific peroxygenase (EC 1.11.2.1) represents a group of secreted hemethiolate proteins that are capable of catalyzing the selective mono-oxygenation of diverse organic compounds using only H2O2 as a cosubstrate. In this study, the peroxygenase from Agrocybe aegerita (AaeUPO) was found to catalyze the hydroxylation of various linear (e.g n-hexane), branched (e.g. 2,3-dimethylbutane) and cyclic alkanes (e.g. cyclohexane). The size of n-alkane substrates converted by AaeUPO ranged from gaseous propane (C3) to n-hexadecane (C16). They were mono-hydroxylated mainly at the C2 and C3 position, ra
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2

Ly, Mai Anh. "Evaluation of components for the heterologous expression of Mycobacterium chubuense NBB4 monooxygenases." Thesis, The University of Sydney, 2014. http://hdl.handle.net/2123/11638.

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Bacterial monooxygenases have important roles in the biogeochemical cycling of carbon and nitrogen, as well as potential applications in biocatalysis of pharmaceutically important epoxides, and bioremediation of chlorinated pollutants. However, use of monooxygenases for biotechnology requires understanding of microbial physiology and the catalytic properties (e.g. substrate range and kinetic parameters) of monooxygenases themselves. Heterologous expression of monooxygenases is one way to advance our fundamental knowledge of MO functions, and also to enable future applications. This project f
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3

Yip, Wing-ping, and 葉永平. "Alkane C-H bond oxidations and alkene dihydroxylations by oxorutheniumcomplexes of chelating tertiary amine ligands." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31246254.

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4

Wagener, Alex [Verfasser], and Stefan [Akademischer Betreuer] Ernst. "Adsorptive Trennung von Gemischen kurzkettiger Alkane und Alkene an nanostrukturierten porösen Adsorbentien / Alex Wagener. Betreuer: Stefan Ernst." Kaiserslautern : Universitätsbibliothek Kaiserslautern, 2012. http://d-nb.info/1021529036/34.

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5

Prat, Casellas Irene. "Bioinspired non-heme iron catalysts for challenging oxidative transformations: mechanistic studies and catalytic applications on selective alkane hydroxylation and alkene cis-dihydroxilation." Doctoral thesis, Universitat de Girona, 2013. http://hdl.handle.net/10803/117778.

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The functionalization of hydrocarbons in a sustainable manner is one of the main challenges for chemists. Their abundance in nature as natural gas or crude oil makes them the most convenient chemical feedstock. The oxidation of hydrocarbons is one of the most interesting reactions, because the introduction of an oxygen atom introduces functionality in these molecules, increasing their value as reagents for further chemical transformation. However, these reactions are fundamentally difficult due to the low reactivity of alkyl C-H bonds. Current available methodologies involve highly reactive-ox
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6

Haak, Edgar. "Titankatalysatoren für die intermolekulare Hydroaminierung von Alkinen und Alkenen." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=964517639.

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7

Groaz, Elisabetta. "Alkene and alkyne metathesis reactions using ruthenium initiators." Thesis, King's College London (University of London), 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.440449.

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8

Mehta, Brinda Mayank. "Green Resins based on Alkene- and Alkyne-containing Triglycerides." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1468795161.

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9

Pongtavornpinyo, Ruti. "Indium Carbenes Alkenes and Alkanes." Thesis, Imperial College London, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.508494.

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10

Edwards, Andrew R. "Polyfluorinated alkenes and alkynes." Thesis, Durham University, 1997. http://etheses.dur.ac.uk/4772/.

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The research described within this thesis may be divided into four main subject areas: 1) The use of (Z)-2H-heptafluorobut-2-ene (10) as a synthon for hexafluorobut- 2-yne (4) in Diels-Alder reactions was investigated. Novel 'one-pot' routes to a variety of bis(trifluoromethyl) substituted furan and arene derivatives were discovered, along with the synthesis of the novel diene, bis(trifluoromethyl)cyclopentadiene (46), from cyclopentadiene.2) A variety of nucleophiles were successfully reacted with (10), the products of which were identical to those that have been, or would be expected to be,
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