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Journal articles on the topic 'Alkenes' oxidation'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Cao, Hongen, Rongrong Qian, and Lei Yu. "Selenium-catalyzed oxidation of alkenes: insight into the mechanisms and developing trend." Catalysis Science & Technology 10, no. 10 (2020): 3113–21. http://dx.doi.org/10.1039/d0cy00400f.

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Recent progresses of the selenium-catalyzed oxidation of alkenes are summarized at the mechanism level. It may be beneficial for designing novel selenium-containing catalysts and alkene oxidation protocols for the next phase of studies.

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2

McClay, Kevin, Brian G. Fox, and Robert J. Steffan. "Toluene Monooxygenase-Catalyzed Epoxidation of Alkenes." Applied and Environmental Microbiology 66, no. 5 (2000): 1877–82. http://dx.doi.org/10.1128/aem.66.5.1877-1882.2000.

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ABSTRACT Several toluene monooxygenase-producing organisms were tested for their ability to oxidize linear alkenes and chloroalkenes three to eight carbons long. Each of the wild-type organisms degraded all of the alkenes that were tested. Epoxides were produced during the oxidation of butene, butadiene, and pentene but not hexene or octadiene. A strain of Escherichia coli expressing the cloned toluene-4-monooxygenase (T4MO) of Pseudomonas mendocina KR1 was able to oxidize butene, butadiene, pentene, and hexene but not octadiene, producing epoxides from all of the substrates that were oxidized

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3

Perez-Benito, Joaquin F., and Donald G. Lee. "Oxidation of hydrocarbons. 15. A study of the oxidation of alkenes by methyltributylammonium permanganate." Canadian Journal of Chemistry 63, no. 12 (1985): 3545–50. http://dx.doi.org/10.1139/v85-582.

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A study of the reduction of methyltributylammonium permanganate by a large number of alkenes in methylene chloride has dispelled a current uncertainty concerning the nature of the inorganic product obtained. It is colloidal manganese dioxide and not a manganate(V) cyclic diester as previously supposed. This product is stabilized in methylene chloride solutions by adsorption of the alkene, which decreases its polarity at the solvent interphase. The solubility of the colloid is therefore a function of both the concentration and the identity of the alkene. In certain (atypical) cases, where acidi

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4

Hajimohammadi, Mahdi, and Nasser Safari. "Photooxygenation of alkenes by molecular oxygen in the presence of porphyrins and chlorin sensitizers under visible light irradiation." Journal of Porphyrins and Phthalocyanines 14, no. 07 (2010): 639–45. http://dx.doi.org/10.1142/s1088424610002446.

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Photooxidation of alkenes by molecular oxygen and visible light in the presence of tetraphenylporphyrin (H2TPP) , tetramesitylporphyrin (H2TMP) , tetrakis pentafluorophenylporphyrin (H2TPFPP) and tetrakis(2,3-dimetoxyphenyl)porphyrin T(2,3-OMeP)P and metalloporphyrins such as ClFeTPP , ClMnTMP , ClMnTPP , ClMnTPFPP , ClCoTPP and ZnTPP has been performed. Photooxidation of alkenes with tetraphenylchlorin (H2TPC) as the sensitizer with visible light has also been studied. The conversion rates for alkene oxidation were in the order of free-base porphyrins > chlorin > metalloporphyrins. In t

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5

Grossi, Vincent, Cristiana Cravo-Laureau, Alain Méou, Danielle Raphel, Frédéric Garzino, and Agnès Hirschler-Réa. "Anaerobic 1-Alkene Metabolism by the Alkane- and Alkene-Degrading Sulfate Reducer Desulfatibacillum aliphaticivorans Strain CV2803T." Applied and Environmental Microbiology 73, no. 24 (2007): 7882–90. http://dx.doi.org/10.1128/aem.01097-07.

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ABSTRACT The alkane- and alkene-degrading, marine sulfate-reducing bacterium Desulfatibacillum aliphaticivorans strain CV2803T, known to oxidize n-alkanes anaerobically by fumarate addition at C-2, was investigated for its 1-alkene metabolism. The total cellular fatty acids of this strain were predominantly C-(even number) (C-even) when it was grown on C-even 1-alkenes and predominantly C-(odd number) (C-odd) when it was grown on C-odd 1-alkenes. Detailed analyses of those fatty acids by gas chromatography-mass spectrometry after 6- to 10-week incubations allowed the identification of saturate

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6

Cermenati, Laura, Maurizio Fagnoni, and Angelo Albini. "TiO2-photocatalyzed reactions of some benzylic donors." Canadian Journal of Chemistry 81, no. 6 (2003): 560–66. http://dx.doi.org/10.1139/v03-048.

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TiO2-photocatalyzed oxidation of toluene (1a), benzyltrimethylsilane (1b), and 4-methoxybenzyltrimethylsilane (1c) has been carried out in acetonitrile under oxygen, under nitrogen, and in the presence of electrophilic alkenes under various conditions (using Ag2SO4 as electron acceptor, adding 2.5% H2O, changing solvent to CH2Cl2). Benzyl radicals, formed via electron transfer and fragmentation, are trapped. A good material balance is often obtained. The overall efficiency of the process depends on the donor Eox, on the rate of fragmentation of the radical cation, and on the acceptor present (

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7

Niku-Paavola, M. L., and L. Viikari. "Enzymatic oxidation of alkenes." Journal of Molecular Catalysis B: Enzymatic 10, no. 4 (2000): 435–44. http://dx.doi.org/10.1016/s1381-1177(99)00117-4.

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8

Mckee, C. S. "Oxidation of higher alkenes." Applied Catalysis A: General 106, no. 2 (1993): N20—N21. http://dx.doi.org/10.1016/0926-860x(93)80185-s.

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9

Teng, A. P., J. D. Crounse, L. Lee, J. M. St. Clair, R. C. Cohen, and P. O. Wennberg. "Hydroxy nitrate production in the OH-initiated oxidation of alkenes." Atmospheric Chemistry and Physics Discussions 14, no. 5 (2014): 6721–57. http://dx.doi.org/10.5194/acpd-14-6721-2014.

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Abstract. Alkenes generally react rapidly by addition of OH and subsequently O2 to form beta hydroxy peroxy radicals. These peroxy radicals react with NO to form beta hydroxy nitrates with a branching ratio α. We quantify α for C2–C8 alkenes at 296 K ±3 and 993 hPa. The branching ratio can be expressed as α = (0.042 ± 0.008) × N − (0.11 ± 0.04) where N is the number of heavy atoms (excluding the peroxy moiety), and listed errors are 2σ. These branching ratios are larger than previously reported and are similar to those for peroxy radicals formed from H abstraction from alkanes. We find the iso

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10

Teng, A. P., J. D. Crounse, L. Lee, J. M. St. Clair, R. C. Cohen, and P. O. Wennberg. "Hydroxy nitrate production in the OH-initiated oxidation of alkenes." Atmospheric Chemistry and Physics 15, no. 8 (2015): 4297–316. http://dx.doi.org/10.5194/acp-15-4297-2015.

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Abstract. Alkenes are oxidized rapidly in the atmosphere by addition of OH and subsequently O2 leading to the formation of β-hydroxy peroxy radicals. These peroxy radicals react with NO to form β-hydroxy nitrates with a branching ratio α. We quantify α for C2–C8 alkenes at 295 K ± 3 and 993 hPa. The branching ratio can be expressed as α = (0.045 ± 0.016) × N − (0.11 ± 0.05) where N is the number of heavy atoms (excluding the peroxy moiety), and listed errors are 2σ. These branching ratios are larger than previously reported and are similar to those for peroxy radicals formed from H abstraction

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11

Gogin, L. L., and E. G. Zhizhina. "Features of the liquid-phase oxidation of alkenes to carbonyl compounds in the presence of palladium compounds." Kataliz v promyshlennosti 1, no. 1-2 (2021): 67–73. http://dx.doi.org/10.18412/1816-0387-2021-1-2-67-73.

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Features of the liquid-phase oxidation of alkenes to ketones or aldehydes in the presence of palladium compounds (Wacker oxidation) are discussed in the review. It is shown that the appropriate reaction conditions, namely, the efficient composition of catalyst, oxidant and solvent, make it possible to selectively produce either ketones or aldehydes from terminal alkenes, and ketones from alkenes with the internal double bond.

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12

Pielichowski, Jan, Grzegorz Kowalski, and Gennady Zaikov. "Catalytic Activity of Polymer-Supported Cobalt(II) Catalysts in the Oxidation of Alkenes." Chemistry & Chemical Technology 5, no. 3 (2011): 303–8. http://dx.doi.org/10.23939/chcht05.03.303.

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13

Stokes, N. J., G. M. Terry, B. J. Tabner, and C. N. Hewitt. "The effects of reactive hydrocarbons on plants." Proceedings of the Royal Society of Edinburgh. Section B. Biological Sciences 102 (1994): 307–11. http://dx.doi.org/10.1017/s0269727000014299.

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Non-methane hydrocarbons (NMHC), of biogenic or anthropogenic origin, are important reactants in most atmospheric environments. Oxidation of NMHC can result indirectly in the formation of ozone (Crutzen 1988). In addition to the direct toxic effects of ozone on plants, reaction of alkenes with ozone can produce organic hydroperoxides which are highly reactive and have been implicated in plant damage, especially in those species which are alkene-emitters (Hewitt et al. 1990a, b).

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14

Zhao, Yating, Zhe Li, Chao Yang, Run Lin, and Wujiong Xia. "Visible-light photoredox catalysis enabled bromination of phenols and alkenes." Beilstein Journal of Organic Chemistry 10 (March 7, 2014): 622–27. http://dx.doi.org/10.3762/bjoc.10.53.

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A mild and efficient methodology for the bromination of phenols and alkenes has been developed utilizing visible light-induced photoredox catalysis. The bromine was generated in situ from the oxidation of Br− by Ru(bpy)3 3+, both of which resulted from the oxidative quenching process.

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15

Liu, Yuanhong. "ChemInform Abstract: Gold-Catalyzed Oxidation Reactions: Oxidation of Alkenes." ChemInform 43, no. 52 (2012): no. http://dx.doi.org/10.1002/chin.201252191.

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16

Sheppard, Tom, Sam Mann, and L. Benhamou. "Palladium(II)-Catalysed Oxidation of Alkenes." Synthesis 47, no. 20 (2015): 3079–117. http://dx.doi.org/10.1055/s-0035-1560465.

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17

Bäumer, U. St, and H. J. Schäfer. "Cleavage of alkenes by anodic oxidation." Journal of Applied Electrochemistry 35, no. 12 (2005): 1283–92. http://dx.doi.org/10.1007/s10800-005-9060-4.

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18

Breton, Tony, Denis Liaigre, and El Mustapha Belgsir. "Allylic oxidation: easy synthesis of alkenones from activated alkenes with TEMPO." Tetrahedron Letters 46, no. 14 (2005): 2487–90. http://dx.doi.org/10.1016/j.tetlet.2005.02.032.

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19

Atmaca, Ufuk, Hande K. Usanmaz, and Murat Çelik. "Oxidations of alkenes with hypervalent iodine reagents: an alternative ozonolysis of phenyl substituted alkenes and allylic oxidation of unsubstituted cyclic alkenes." Tetrahedron Letters 55, no. 14 (2014): 2230–32. http://dx.doi.org/10.1016/j.tetlet.2014.02.076.

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20

Rayati, Saeed, and Zahra Sheybanifard. "Ultrasound promoted green oxidation of alkenes with hydrogen peroxide in the presence of iron porphyrins supported on multi-walled carbon nanotubes." Journal of Porphyrins and Phthalocyanines 19, no. 04 (2015): 622–30. http://dx.doi.org/10.1142/s1088424615500030.

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In the present work, oxidation of alkenes with hydrogen peroxide in the presence of meso-tetrakis(4-hydroxyphenyl)porphyrinatoiron(III) chloride supported onto surface of functionalized multi-wall carbon nanotubes (FMWCNT), [ Fe ( THPP ) Cl@MWCNT ], is reported. The simple heterogeneous catalyst was characterized by FT-IR spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and also thermal analysis. The amount of the catalyst loaded on the nanotubes was determined by atomic absorption spectroscopy. This heterogeneous catalyst proved to be an efficient and g

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21

Krahe, Nina-Katharina, Ralf G. Berger, and Franziska Ersoy. "A DyP-Type Peroxidase of Pleurotus sapidus with Alkene Cleaving Activity." Molecules 25, no. 7 (2020): 1536. http://dx.doi.org/10.3390/molecules25071536.

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Alkene cleavage is a possibility to generate aldehydes with olfactory properties for the fragrance and flavor industry. A dye-decolorizing peroxidase (DyP) of the basidiomycete Pleurotus sapidus (PsaPOX) cleaved the aryl alkene trans-anethole. The PsaPOX was semi-purified from the mycelium via FPLC, and the corresponding gene was identified. The amino acid sequence as well as the predicted tertiary structure showed typical characteristics of DyPs as well as a non-canonical Mn2+-oxidation site on its surface. The gene was expressed in Komagataella pfaffii GS115 yielding activities up to 142 U/L

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22

Monos, Timothy M., Rory C. McAtee, and Corey R. J. Stephenson. "Arylsulfonylacetamides as bifunctional reagents for alkene aminoarylation." Science 361, no. 6409 (2018): 1369–73. http://dx.doi.org/10.1126/science.aat2117.

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Alkene aminoarylation with a single, bifunctional reagent is a concise synthetic strategy. We report a catalytic protocol for the addition of arylsulfonylacetamides across electron-rich alkenes with complete anti-Markovnikov regioselectivity and excellent diastereoselectivity to provide 2,2-diarylethylamines. In this process, single-electron alkene oxidation enables carbon-nitrogen bond formation to provide a key benzylic radical poised for a Smiles-Truce 1,5-aryl shift. This reaction is redox-neutral, exhibits broad functional group compatibility, and occurs at room temperature with loss of s

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23

Huo, Congde, Yajun Wang, Yong Yuan, Fengjuan Chen, and Jing Tang. "Auto-oxidative hydroxysulfenylation of alkenes." Chemical Communications 52, no. 45 (2016): 7233–36. http://dx.doi.org/10.1039/c6cc01937d.

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24

Kong, De-Long, Jian-Xun Du, Wei-Ming Chu, Chun-Ying Ma, Jia-Yi Tao, and Wen-Hua Feng. "Ag/Pyridine Co-Mediated Oxidative Arylthiocyanation of Activated Alkenes." Molecules 23, no. 10 (2018): 2727. http://dx.doi.org/10.3390/molecules23102727.

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An efficient Ag/pyridine co-mediated oxidative arylthiocyanation of activated alkenes via radical addition/cyclization cascade process was developed. This reaction could be carried out under mild conditions to provide biologically interesting 3-alkylthiocyanato-2-oxindoles in good to excellent yields. Mechanistic studies suggested a unique NCS• radical addition path and clarified the dual roles of catalytic pyridine as base and crucial ligand to accelerate the oxidation of Ag(I) to Ag(II), which is likely oxidant responsible for the formation of NCS• radical. These mechanistic results may impa

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25

Kabalka, George W., Su Yu, and Nan-Sheng Li. "Selective hydroboration of alkenes and alkynes in the presence of aldehydes and ketones." Canadian Journal of Chemistry 76, no. 6 (1998): 800–805. http://dx.doi.org/10.1139/v98-042.

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The reactions of terminal alkenes in the presence of ketones or aldehydes with a variety of borane reagents have been investigated. It was found that the selective hydroboration of a terminal alkene in the presence of a ketone or an aldehyde is most efficient when dicyclohexylborane is used as the hydroborating agent. The hydroboration of olefinic ketones and olefinic aldehydes with dicyclohexylborane generates the corresponding hydroxyaldehydes and hydroxyketones in good yields after oxidation with sodium perborate. The hydroboration of alkynyl ketones and alkynyl aldehydes with dicyclohexylb

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26

Perumal, P. Thirumalai. "Oxidation of Alkenes by Peroxydisulphate-copper Sulphate." Synthetic Communications 20, no. 9 (1990): 1353–56. http://dx.doi.org/10.1080/00397919008052848.

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27

Guerra, Francisco, Ana García-Cabeza, F. Moreno-Dorado, and María Ortega. "Copper-Catalyzed Oxidation of Alkenes and Heterocycles." Synthesis 48, no. 15 (2016): 2323–42. http://dx.doi.org/10.1055/s-0035-1561649.

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28

Heyberger, Barbara, Najib Belmekki, Val�rie Conraud, Pierre-Alexandre Glaude, Ren� Fournet, and Fr�d�rique Battin-Leclerc. "Oxidation of small alkenes at high temperature." International Journal of Chemical Kinetics 34, no. 12 (2002): 666–77. http://dx.doi.org/10.1002/kin.10092.

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29

Moiseev, I. I., and M. N. Vargaftik. "Allylic oxidation of alkenes with palladium catalysts." Coordination Chemistry Reviews 248, no. 21-24 (2004): 2381–91. http://dx.doi.org/10.1016/j.ccr.2004.05.020.

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30

Alshammari, Hamed, Peter J. Miedziak, Thomas E. Davies, David J. Willock, David W. Knight, and Graham J. Hutchings. "Initiator-free hydrocarbon oxidation using supported gold nanoparticles." Catal. Sci. Technol. 4, no. 4 (2014): 908–11. http://dx.doi.org/10.1039/c4cy00088a.

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31

Atmaca, Ufuk, Hande K. Usanmaz, and Murat Celik. "ChemInform Abstract: Oxidations of Alkenes with Hypervalent Iodine Reagents: An Alternative Ozonolysis of Phenyl Substituted Alkenes and Allylic Oxidation of Unsubstituted Cyclic Alkenes." ChemInform 45, no. 37 (2014): no. http://dx.doi.org/10.1002/chin.201437043.

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32

Sun, Wuchuan, Yingjia Zhang, Yang Li, and Zuohua Huang. "Hierarchical Auto-Ignition and Structure-Reactivity Trends of C2–C4 1-Alkenes." Energies 14, no. 18 (2021): 5797. http://dx.doi.org/10.3390/en14185797.

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Ignition delay times of small alkenes are a valuable constraint for the refinement of the core kinetic mechanism of hydrocarbons used in representing combustion properties of real fuels. Moreover, the chemical reactivity comparison of those small alkenes provides a reference in object-oriented fuel design and logical combustion utilization. In this study, the ignition delay times of C2–C4 alkenes (ethylene, propene and 1-butene) were measured behind reflected shock waves first, with a fixed oxygen concentration (XO2 = 6%) and equivalence ratio (φ = 1.0) at various pressures of 1.2, 4.0 and 16.

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33

Otsuka, Kiyoshi, Ichiro Yamanaka, and Akio Nishi. "An Alkene-NO[sub x] Cell for the Wacker-Type Oxidation of Alkenes." Journal of The Electrochemical Society 148, no. 2 (2001): D4. http://dx.doi.org/10.1149/1.1337612.

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34

Elshorbany, Y. F., R. Kurtenbach, P. Wiesen, et al. "Oxidation capacity of the city air of Santiago, Chile." Atmospheric Chemistry and Physics 9, no. 6 (2009): 2257–73. http://dx.doi.org/10.5194/acp-9-2257-2009.

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Abstract. The oxidation capacity of the highly polluted urban area of Santiago, Chile has been evaluated during a summer measurement campaign carried out from 8–20 March 2005. The hydroxyl (OH) radical budget was evaluated employing a simple quasi-photostationary-state model (PSS) constrained with simultaneous measurements of HONO, HCHO, O3, NO, NO2, j(O1D), j(NO2), 13 alkenes and meteorological parameters. In addition, a zero dimensional photochemical box model based on the Master Chemical Mechanism (MCMv3.1) has been used to estimate production rates and total free radical budgets, including

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35

Elshorbany, Y. F., R. Kurtenbach, P. Wiesen, et al. "Oxidation capacity of the city air of Santiago, Chile." Atmospheric Chemistry and Physics Discussions 8, no. 6 (2008): 19123–71. http://dx.doi.org/10.5194/acpd-8-19123-2008.

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Abstract. The oxidation capacity of the highly polluted urban area of Santiago, Chile has been evaluated during an extensive summer measurement campaign carried out from 8–20 March 2005. The hydroxyl (OH) radical budget was evaluated employing a simple quasi-photostationary-state model (PSS) constrained with simultaneous measurements of HONO, HCHO, O3, NO, NO2, j(O1D), j(NO2), 13 alkenes and meteorological parameters. In addition, a zero dimensional photochemical box model based on the Master Chemical Mechanism (MCMv3.1) has been used to estimate production rates and total free radical budgets

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36

Zhao, JinWu, Li Liu, ShiJian Xiang, Qiang Liu, and HuoJi Chen. "Direct conversion of allyl arenes to aryl ethylketones via a TBHP-mediated palladium-catalyzed tandem isomerization–Wacker oxidation of terminal alkenes." Organic & Biomolecular Chemistry 13, no. 20 (2015): 5613–16. http://dx.doi.org/10.1039/c5ob00586h.

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37

Tabor, John R., Derek C. Obenschain, and Forrest E. Michael. "Selenophosphoramide-catalyzed diamination and oxyamination of alkenes." Chemical Science 11, no. 6 (2020): 1677–82. http://dx.doi.org/10.1039/c9sc05335b.

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38

Xu, Jun, Yilan Zhang, Xiaoguang Yue, Jie Huo, Daokai Xiong, and Pengfei Zhang. "Selective oxidation of alkenes to carbonyls under mild conditions." Green Chemistry 23, no. 15 (2021): 5549–55. http://dx.doi.org/10.1039/d1gc01364e.

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This study demonstrates a photo-induced and tetrahydrofuran (THF)-based radical strategy for the selective oxidation of alkenes to carbonyls using O<sub>2</sub> as the sole oxidant and water as the sole solvent.

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39

Zhang, Jian, Weiwei Jin, Cungui Cheng, and Fang Luo. "Copper-catalyzed remote oxidation of alcohols initiated by radical difluoroalkylation of alkenes: facile access to difluoroalkylated carbonyl compounds." Organic & Biomolecular Chemistry 16, no. 21 (2018): 3876–80. http://dx.doi.org/10.1039/c8ob00889b.

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40

Yap, Chew Pheng, Jing Kuang Ng, Sherzod Madrahimov, Ashfaq A. Bengali, Tsz Sian Chwee, and Wai Yip Fan. "Oxidation of aromatic alkenes and alkynes catalyzed by a hexa-acetonitrile iron(ii) ionic complex [Fe(CH3CN)6][BF4]2." New Journal of Chemistry 42, no. 13 (2018): 11131–36. http://dx.doi.org/10.1039/c8nj02226g.

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41

Vincent, Jean-Marc, Alain Rabion, Vittal K. Yachandra, and Richard H. Fish. "Fluorous biphasic catalysis. 2. Synthesis of fluoroponytailed amine ligands along with fluoroponytailed carboxylate synthons, [M(C8F17(CH2)2CO2)2] (M = Mn2+ or Co2+): Demonstration of a perfluoroheptane soluble precatalyst for alkane and alkene functionalization in the presence of tert-butyl hydroperoxide and oxygen gas." Canadian Journal of Chemistry 79, no. 5-6 (2001): 888–95. http://dx.doi.org/10.1139/v01-012.

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Fluorous biphasic catalysis (FBC) is a relatively new concept for homogeneous catalysis where the fluorocarbon soluble catalyst resides in a separate phase from the substrate and products. Therefore, separation of the catalyst and the products occurs by a facile decantation process. In this contribution, we present the synthesis of new Rf-fluoroponytailed synthons, 2-iodo-1-perfluorooctyl-3-propanol (1), 3-perfluorooctyl-1-propanol (2), and 3-perfluorooctyl-1-iodopropane (3), a variety of new Rf-fluoroponytailed ligands (48), with starting amines, 1,4,7-triazacyclononane, bis-picolylamine, an

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42

Nunes, Carla D., Pedro D. Vaz, Vítor Félix, et al. "Vanadyl cationic complexes as catalysts in olefin oxidation." Dalton Transactions 44, no. 11 (2015): 5125–38. http://dx.doi.org/10.1039/c4dt03174a.

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43

Haddadi, Hedayat, Shahrbanou Moradpour Hafshejani, Mostafa Riahi Farsani, and Ali Kazemi Babahydari. "Heterogeneous epoxidation of alkenes with H2O2 catalyzed by a recyclable organic–inorganic polyoxometalate-based framework catalyst." New Journal of Chemistry 39, no. 12 (2015): 9879–85. http://dx.doi.org/10.1039/c5nj01661d.

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44

Anees, M., S. Nayak, K. Afarinkia, and V. Vinader. "Control of the stereochemistry of C14 hydroxyl during the total synthesis of withanolide E and physachenolide C." RSC Advances 8, no. 69 (2018): 39691–95. http://dx.doi.org/10.1039/c8ra08540d.

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45

Ramanathan, Mani, Jing Wan, and Shiuh-Tzung Liu. "Preparation of 3-hydroxyquinolines from direct oxidation of dihydroquinolinium salts." RSC Advances 8, no. 67 (2018): 38166–74. http://dx.doi.org/10.1039/c8ra07940d.

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46

Peral, Daniel, Daniel Herrera, Julio Real, Teresa Flor та J. Carles Bayón. "Strong π-acceptor sulfonated phosphines in biphasic rhodium-catalyzed hydroformylation of polar alkenes". Catalysis Science & Technology 6, № 3 (2016): 800–808. http://dx.doi.org/10.1039/c5cy01004g.

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47

Brazdil, James F. "Scheelite: a versatile structural template for selective alkene oxidation catalysts." Catalysis Science & Technology 5, no. 7 (2015): 3452–58. http://dx.doi.org/10.1039/c5cy00387c.

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Wang, Na, Liu Ye, Zhong-Liang Li, et al. "Hydrofunctionalization of alkenols triggered by the addition of diverse radicals to unactivated alkenes and subsequent remote hydrogen atom translocation." Organic Chemistry Frontiers 5, no. 19 (2018): 2810–14. http://dx.doi.org/10.1039/c8qo00734a.

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Kaur, Richie, Brandi M. Hudson, Joseph Draper, Dean J. Tantillo, and Cort Anastasio. "Aqueous reactions of organic triplet excited states with atmospheric alkenes." Atmospheric Chemistry and Physics 19, no. 7 (2019): 5021–32. http://dx.doi.org/10.5194/acp-19-5021-2019.

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Abstract:

Abstract. Triplet excited states of organic matter are formed when colored organic matter (i.e., brown carbon) absorbs light. While these “triplets” can be important photooxidants in atmospheric drops and particles (e.g., they rapidly oxidize phenols), very little is known about their reactivity toward many classes of organic compounds in the atmosphere. Here we measure the bimolecular rate constants of the triplet excited state of benzophenone (3BP∗), a model species, with 17 water-soluble C3–C6 alkenes that have either been found in the atmosphere or are reasonable surrogates for identified

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Tressler, Caitlin M., Peter Stonehouse, and Keith S. Kyler. "Calcium tungstate: a convenient recoverable catalyst for hydrogen peroxide oxidation." Green Chemistry 18, no. 18 (2016): 4875–78. http://dx.doi.org/10.1039/c6gc00725b.

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