Results 351 to 360 of about 196,361 (378)
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Catalytic functionalization of arenes and alkanes via C-H bond activation.
Accounts of Chemical Research, 2001Several novel synthetic reactions of arenes and alkanes discovered and investigated in our laboratory are summarized here. These include olefin arylation, hydroarylation of alkynes, hydroxylation of arenes, carboxylation of arenes and alkanes, and ...
Chengguo Jia, T. Kitamura, Y. Fujiwara
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A free radical cascade cyclization of isocyanides with simple alkanes and alcohols.
Organic Letters, 2014A copper-catalyzed free-radical cascade cyclization of isocyanides with simple alkanes and alcohols was developed, which allowed convenient access to various alkyl-substituted phenanthridines.
Zejiang Li +3 more
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Gas-Phase Tropospheric Chemistry of Volatile Organic Compounds: 1. Alkanes and Alkenes
, 1997Literature data (through mid-1996) concerning the gas-phase reactions of alkanes and alkenes (including isoprene and monoterpenes) leading to their first generation products are reviewed and evaluated for tropospheric conditions.
R. Atkinson
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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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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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