Results 211 to 220 of about 102,008 (242)
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Towards a practical development of light-driven acceptorless alkane dehydrogenation.
Angewandte Chemie, 2014The efficient catalytic dehydrogenation of alkanes to olefins is one of the most investigated reactions in organic synthesis. In the coming years, an increased supply of shorter-chain alkanes from natural and shale gas will offer new opportunities for ...
A. Chowdhury +5 more
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Metabolism of Alkanes by Yeasts
1981One of the specific features of alkane-utilizing yeasts is the conspicuous appearance of peroxisomes. This review describes the metabolism of alkanes in yeasts with special emphasis on the physiological function of peroxisomes. The subtle diversity in alkane utilization pathway in yeasts is mediated by subcellular localization of enzymes.
S. Fukui, A. Tanaka
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1978
In 1849 [1] Kolbe attempted to isolate the methyl radical via the electrolysis of an aqueous solution of potassium acetate. The hydrocarbon he obtained is now known to be ethane, but further investigations into the electrolysis of the alkali metal salts of aliphatic carboxylic acids have shown the reaction to have considerable utility for the synthesis
Maxwell James Parrott, David I. Davies
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In 1849 [1] Kolbe attempted to isolate the methyl radical via the electrolysis of an aqueous solution of potassium acetate. The hydrocarbon he obtained is now known to be ethane, but further investigations into the electrolysis of the alkali metal salts of aliphatic carboxylic acids have shown the reaction to have considerable utility for the synthesis
Maxwell James Parrott, David I. Davies
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Efficiency enhancement in low-bandgap polymer solar cells by processing with alkane dithiols.
Nature Materials, 2007J. Peet +6 more
semanticscholar +1 more source
1948
Publisher Summary This chapter describes the isomerization of butanes, pentanes, hexanes, heptanes, and higher alkanes. The need for isobutane as a charging stock for alkylation processes and the necessity for converting low octane number straight chain hydrocarbons to their higher octane number branched chain isomers, gives an impetus to the study ...
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Publisher Summary This chapter describes the isomerization of butanes, pentanes, hexanes, heptanes, and higher alkanes. The need for isobutane as a charging stock for alkylation processes and the necessity for converting low octane number straight chain hydrocarbons to their higher octane number branched chain isomers, gives an impetus to the study ...
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2009
This chapter covers oxidation of C–H and C–C bonds in alkanes. Section 4.1 concerns oxidation of C–H bonds: aldehydes and other CH species (4.1.1), methylene (–CH2 groups) (4.1.2) and methyl (–CH3) groups (4.1.3). This is followed by the oxidation of cyclic alkanes (4.1.4) and large-scale alkane oxidations (4.1.5). Alkane oxidations not considered here
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This chapter covers oxidation of C–H and C–C bonds in alkanes. Section 4.1 concerns oxidation of C–H bonds: aldehydes and other CH species (4.1.1), methylene (–CH2 groups) (4.1.2) and methyl (–CH3) groups (4.1.3). This is followed by the oxidation of cyclic alkanes (4.1.4) and large-scale alkane oxidations (4.1.5). Alkane oxidations not considered here
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Expanding anaerobic alkane metabolism in the domain of Archaea
Nature Microbiology, 2019Yinzhao Wang +4 more
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Carbon dioxide reduction in tandem with light-alkane dehydrogenation
Nature Reviews Chemistry, 2019Elaine Gomez +3 more
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