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Journal articles on the topic 'Alkenes and tertiary recovery'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Felber, Betty. "Overview: Tertiary Recovery (January 2002)." Journal of Petroleum Technology 54, no. 01 (2002): 48. http://dx.doi.org/10.2118/0102-0048-jpt.

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2

Felber, Betty. "Overview: Tertiary Recovery (January 2003)." Journal of Petroleum Technology 55, no. 01 (2003): 54. http://dx.doi.org/10.2118/0103-0054-jpt.

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3

Geik, Dennis, Michael Rosien, Jens Bielefeld, Marc Schmidtmann, and Sven Doye. "Titanium‐Catalyzed Intermolecular Hydroaminoalkylation of Alkenes with Tertiary Amines." Angewandte Chemie 133, no. 18 (2021): 10024–28. http://dx.doi.org/10.1002/ange.202100431.

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4

Geik, Dennis, Michael Rosien, Jens Bielefeld, Marc Schmidtmann, and Sven Doye. "Titanium‐Catalyzed Intermolecular Hydroaminoalkylation of Alkenes with Tertiary Amines." Angewandte Chemie International Edition 60, no. 18 (2021): 9936–40. http://dx.doi.org/10.1002/anie.202100431.

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5

Budi, Iwan Setya, Agus Rudiyono, and Astra Pramana Astra Pramana. "INJEKSI FOAM SEBAGAI TERTIARY OIL RECOVERY." PETRO:Jurnal Ilmiah Teknik Perminyakan 8, no. 2 (2019): 51. http://dx.doi.org/10.25105/petro.v8i2.4774.

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<p><em>Foam injection is a variance of gas flood as tertiary recovery method designed to mitigate low sweep efficiency normally found in gas flood due to inheritance of density difference between injected gas and oil which often severed by presence of reservoir heterogeneity (permeability contrast in this case). Foam EOR has two goals: (1) improve oil recovery by promoting better sweep efficiency, and (2) reduce carbon emission related to global warming issue provided that the injectant gas used is CO2, hydrocarbon gas or flue gas.. Reservoir simulation performed is able to show re

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6

Li, Ganzuo, Limin Zhai, Guiying Xu, Qiang Shen, Hongzhi Mao, and Meishan Pei. "CURRENT TERTIARY OIL RECOVERY IN CHINA." Journal of Dispersion Science and Technology 21, no. 4 (2000): 367–408. http://dx.doi.org/10.1080/01932690008913277.

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7

Song, Zengqiang, та Andrey P. Antonchick. "Catching α-aminoalkyl radicals: cyclization between tertiary alkylanilines and alkenes". Tetrahedron 72, № 48 (2016): 7715–21. http://dx.doi.org/10.1016/j.tet.2016.04.052.

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8

Hoffmann, Norbert, Samuel Bertrand, Siniša Marinković, and Jens Pesch. "Efficient radical addition of tertiary amines to alkenes using photochemical electron transfer." Pure and Applied Chemistry 78, no. 12 (2006): 2227–46. http://dx.doi.org/10.1351/pac200678122227.

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An efficient photoinduced radical addition of tertiary amine, mainly cyclic derivatives, to electron-deficient alkenes was developed. The reaction was applied to the asymmetric synthesis of the pyrrolizidine alkaloids laburnine and isoretronecanol. The method was then optimized for the addition of a larger variety of tertiary amines, in particular acyclic ones. Radical tandem addition cyclization reactions with unsaturated tertiary amines have also been investigated. A detailed mechanistic study using isotopic labeling enabled the optimization of a corresponding reaction with N,N-dialkylanilin

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9

Alvarez-Manzaneda, E. J., R. Chahboun, E. Cabrera Torres, et al. "Synthesis of alkenes from tertiary esters utilizing the triphenylphosphine–iodine system." Tetrahedron Letters 46, no. 7 (2005): 1075–77. http://dx.doi.org/10.1016/j.tetlet.2004.12.104.

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10

Lu, Qingquan, Jian Zhang, Fuliang Wei та ін. "Aerobic Oxysulfonylation of Alkenes Leading to Secondary and Tertiary β-Hydroxysulfones". Angewandte Chemie International Edition 52, № 28 (2013): 7156–59. http://dx.doi.org/10.1002/anie.201301634.

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11

Lu, Qingquan, Jian Zhang, Fuliang Wei та ін. "Aerobic Oxysulfonylation of Alkenes Leading to Secondary and Tertiary β-Hydroxysulfones". Angewandte Chemie 125, № 28 (2013): 7297–300. http://dx.doi.org/10.1002/ange.201301634.

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12

Zeng, Hao, Chuanle Zhu, Chi Liu, Yingying Cai, Fulin Chen та Huanfeng Jiang. "Three component hydroxyletherification and hydroxylazidation of (trifluoromethyl)alkenes: access to α-trifluoromethyl β-heteroatom substituted tertiary alcohols". Chemical Communications 56, № 46 (2020): 6241–44. http://dx.doi.org/10.1039/d0cc02550j.

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The three component hydroxyletherification and hydroxylazidation reactions of (trifluoromethyl)alkenes are reported, providing various useful α-trifluoromethyl β-heteroatom substituted tertiary alcohols in high yields.

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13

van der Schaaf, Paul A., Jean-Pascal Sutter, Mary Grellier, et al. "Palladium-Mediated Intramolecular C-N Bond Formation between Tertiary Amines and Alkenes." Journal of the American Chemical Society 116, no. 12 (1994): 5134–44. http://dx.doi.org/10.1021/ja00091a016.

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14

Li, Qiankun, Wu Fan, Deqian Peng, et al. "Cobalt–Tertiary-Amine-Mediated Hydroxytrifluoromethylation of Alkenes with CF3Br and Atmospheric Oxygen." ACS Catalysis 10, no. 7 (2020): 4012–18. http://dx.doi.org/10.1021/acscatal.0c00498.

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15

Tenaglia, Alphonse, and Sylvain Marc. "CpRuCl(PPh3)2-Catalyzed Cyclopropanation of Bicyclic Alkenes with Tertiary Propargylic Acetates." Journal of Organic Chemistry 71, no. 9 (2006): 3569–75. http://dx.doi.org/10.1021/jo060276a.

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16

Chen, Yan-yan, Xue-jing Zhang, Hui-min Yuan, Wen-tao Wei, and Ming Yan. "Efficient cyclization of tertiary amines and alkenes promoted by KOt-Bu–DMF." Chemical Communications 49, no. 93 (2013): 10974. http://dx.doi.org/10.1039/c3cc46340k.

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17

Khamrai, Jagadish, Saikat Das, Aleksandr Savateev, Markus Antonietti, and Burkhard König. "Mizoroki–Heck type reactions and synthesis of 1,4-dicarbonyl compounds by heterogeneous organic semiconductor photocatalysis." Green Chemistry 23, no. 5 (2021): 2017–24. http://dx.doi.org/10.1039/d0gc03792c.

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We report the synthesis of 1,4-dicarbonyl compounds and substituted alkenes (Mizoroki–Heck type coupling) starting from secondary and tertiary alkyl halides and vinyl acetate or styrene derivatives using visible-light photocatalysis.

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18

Iglauer, Stefan, Yongfu Wu, Patrick Shuler, Yongchun Tang, and William A. Goddard. "New surfactant classes for enhanced oil recovery and their tertiary oil recovery potential." Journal of Petroleum Science and Engineering 71, no. 1-2 (2010): 23–29. http://dx.doi.org/10.1016/j.petrol.2009.12.009.

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19

Ye, Zhi-Peng, Jie Gao, Xin-Yu Duan та ін. "Electrochemical heterodifunctionalization of α-CF3 alkenes to access α-trifluoromethyl-β-sulfonyl tertiary alcohols". Chemical Communications 57, № 71 (2021): 8969–72. http://dx.doi.org/10.1039/d1cc03288g.

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An unprecedented electrochemical heterodifunctionalization of α-CF3 alkenes with benzenesulfonyl hydrazides was accomplished in this work, wherein a β-sulfonyl and a α-hydroxyl group were simultaneously incorporated across the olefinic double bond in a single operation.

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20

Cunico, Robert F., та Adalie Rodriguez Motta. "Addition of Carbamoylsilanes to Electrophilically Substituted Alkenes. Preparation of β-Functionalized Tertiary Amides". Organic Letters 7, № 5 (2005): 771–74. http://dx.doi.org/10.1021/ol040066p.

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21

Salin, Alexey V. "Mechanistic insights into phospha–Michael reaction of tertiary phosphines with electron-deficient alkenes." Phosphorus, Sulfur, and Silicon and the Related Elements 191, no. 11-12 (2016): 1625–27. http://dx.doi.org/10.1080/10426507.2016.1217222.

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22

Rozhkov, I. N., S. M. Igumnov, S. I. Pletnev, and I. V. Chaplina. "Nucleophilic catalysis of the addition of tertiary perfluoroalkyl bromides to alkenes and alkynes." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 39, no. 4 (1990): 856. http://dx.doi.org/10.1007/bf00960371.

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23

Lu, Qingquan, Jian Zhang, Fuliang Wei та ін. "ChemInform Abstract: Aerobic Oxysulfonylation of Alkenes Leading to Secondary and Tertiary β-Hydroxysulfones." ChemInform 44, № 48 (2013): no. http://dx.doi.org/10.1002/chin.201348104.

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24

Dove, H., and M. Oliván. "The possible use of the alkenes (unsaturated hydrocarbons) of plant cuticular wax as diet composition markers in sheep." BSAP Occasional Publication 34 (2006): 1–7. http://dx.doi.org/10.1017/s1463981500042187.

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SummaryThe objective of the current study was to investigate the possible use of alkenes (unsaturated hydrocarbons) of plant waxes as diet composition markers in sheep. Twenty-four sheep (30 kg live weight) were housed in individual pens (n=16, “pen” sheep) or in metabolism crates (n=8, “crate” sheep) for the total collection of faeces. Once daily, sheep were fed 720 g DM of a two-component diet consisting of a roughage source (chaffed perennial ryegrass) and a high-quality supplement (unpelleted sunflower meal, SFM) in different proportions, 7:1, 6:2, 5:3 and 4:4 (4 pen sheep and 2 crate shee

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25

Bange, Christine A., Michael B. Ghebreab, Arne Ficks, Neil T. Mucha, Lee Higham, and Rory Waterman. "Zirconium-catalyzed intermolecular hydrophosphination using a chiral, air-stable primary phosphine." Dalton Transactions 45, no. 5 (2016): 1863–67. http://dx.doi.org/10.1039/c5dt03544a.

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Catalytic hydrophosphination of alkenes using a chiral, air-stable primary phosphine, (R)-MeO-MOPH<sub>2</sub>, proceeds under mild conditions with a zirconium catalyst to selectively furnish anti-Markovnikov, air-stable secondary phosphine or tertiary phosphine prodcuts with slight modification of the protocol.

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26

Cheng, Fengchang, Wenxin Lu, Wei Huang, Lu Wen, Mingfeng Li, and Fanke Meng. "Cu-catalyzed enantioselective synthesis of tertiary benzylic copper complexes and their in situ addition to carbonyl compounds." Chemical Science 9, no. 22 (2018): 4992–98. http://dx.doi.org/10.1039/c8sc00827b.

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Catalytic chemo- and enantioselective generation of tertiary benzylic copper complexes from Cu–B(pin) (pin = pinacolato) additions to 1,1-disubstituted alkenes followed by in situ reactions with ketones and carboxylic acid phenol esters to construct multifunctional alkylboron compounds that contain quaternary stereogenic centers is presented.

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27

Yin, Dai Yin, Bo Ying, Wei Zhou, and Cheng Li Zhang. "Numerical Simulation Optimization Study on Adjusting Well Pattern and Productive Series in Xingqi Area." Advanced Materials Research 616-618 (December 2012): 669–73. http://dx.doi.org/10.4028/www.scientific.net/amr.616-618.669.

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In order to optimize space of tertiary infill wells and tertiary recovery wells, this paper applies numerical simulation method to study Xingqi Area in Daqing oil field. According to serious lateral and vertical heterogeneity and different control degree of water flooding in different parts of reservoir, 3 development schemes are designed. Numerical simulation results show that Scheme 2 is the best, whose well pattern consists of tertiary infill wells and tertiary recovery wells. When water cut is 98%, the ultimate recovery reaches 58.66%, which is 10.74% higher than the ultimate recovery of o

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28

Wang, Zhengbo, Qiang Wang, Desheng Ma, Wanchun Zhao, Xiaohan Feng, and Zhaoxia Liu. "The Fast Potential Evaluation Method of Enhanced Oil Recovery Based on Statistical Analysis." Processes 7, no. 11 (2019): 795. http://dx.doi.org/10.3390/pr7110795.

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Based on a large number of empirical statistics of tertiary oil recovery technology in China, including polymer flooding, chemical flooding, gas flooding, in situ combustion, steam flooding, ect., 22 key reservoir parameters were filterized. Five levels of quantitative screening criteria were developed for different tertiary oil recovery methods. The mean algorithm for the downward approximation and the grey correlation theory were used in this paper to quickly select the appropriate tertiary oil recovery method for the target blocks, which provides a preferred development method for subsequen

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29

Banik, Steven M., Jonathan William Medley, and Eric N. Jacobsen. "Catalytic, asymmetric difluorination of alkenes to generate difluoromethylated stereocenters." Science 353, no. 6294 (2016): 51–54. http://dx.doi.org/10.1126/science.aaf8078.

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Difluoromethyl groups possess specific steric and electronic properties that invite their use as chemically inert surrogates of alcohols, thiols, and other polar functional groups important in a wide assortment of molecular recognition processes. We report here a method for the catalytic, asymmetric, migratory geminal difluorination of β-substituted styrenes to access a variety of products bearing difluoromethylated tertiary or quaternary stereocenters. The reaction uses commercially available reagents (m-chloroperbenzoic acid and hydrogen fluoride pyridine) and a simple chiral aryl iodide cat

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30

Chakrabarty, Suman, and James M. Takacs. "Synthesis of Chiral Tertiary Boronic Esters: Phosphonate-Directed Catalytic Asymmetric Hydroboration of Trisubstituted Alkenes." Journal of the American Chemical Society 139, no. 17 (2017): 6066–69. http://dx.doi.org/10.1021/jacs.7b02324.

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31

HANSON, J. R., P. B. HITCHCOCK, M. D. LIMAN, and R. MANICKAVASAGAR. "ChemInform Abstract: The Effect of a Tertiary Amine in the Catalytic Osmylation of Alkenes." ChemInform 26, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199522252.

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32

Chen, Yan-yan, Xue-jing Zhang, Hui-min Yuan, Wen-tao Wei, and Ming Yan. "ChemInform Abstract: Efficient Cyclization of Tertiary Amines and Alkenes Promoted by KOt-Bu-DMF." ChemInform 45, no. 13 (2014): no. http://dx.doi.org/10.1002/chin.201413032.

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33

VAN DER SCHAAF, P. A., J. P. SUTTER, M. GRELLIER, et al. "ChemInform Abstract: Palladium-Mediated Intramolecular C-N Bond Formation Between Tertiary Amines and Alkenes." ChemInform 25, no. 47 (2010): no. http://dx.doi.org/10.1002/chin.199447059.

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34

Rucker, Richard P., Aaron M. Whittaker, Hester Dang, and Gojko Lalic. "Synthesis of Tertiary Alkyl Amines from Terminal Alkenes: Copper-Catalyzed Amination of Alkyl Boranes." Journal of the American Chemical Society 134, no. 15 (2012): 6571–74. http://dx.doi.org/10.1021/ja3023829.

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35

Marinković, Siniša, and Norbert Hoffmann. "Semiconductors as sensitisers for the radical addition of tertiary amines to electron deficient alkenes." International Journal of Photoenergy 5, no. 3 (2003): 175–82. http://dx.doi.org/10.1155/s1110662x03000308.

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Using heterogeneous photocatalysis, the radical addition of tertiary amines with electron deficient alkenes can be performed in high yields (up to 98%) and high facial diastereoselectivity. The photochemical induced electron transfer process initiates the radical chain reaction and inorganic semiconductors likeTiO2and ZnS were used. According to the proposed mechanism, the reaction takes place at the surface of the semiconductor and the termination step results from an interfacial electron transfer from the conduction band to the oxoallyl radical intermediate. Frequently, semiconductors are us

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36

Bibouche, Bachir, Daniel Peral, Dmitrij Stehl, et al. "Multiphasic aqueous hydroformylation of 1-alkenes with micelle-like polymer particles as phase transfer agents." RSC Advances 8, no. 41 (2018): 23332–38. http://dx.doi.org/10.1039/c8ra04022b.

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Micelle-like polyelectrolyte polymer particles were applied as phase transfer agents and catalyst carriers in the multiphasic hydroformylation of long chain alkenes achieving high turnover frequencies and efficient catalyst recovery.

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37

Du, Yi-Dan, Chun-Wai Tse, Zhen-Jiang Xu, Yungen Liu, and Chi-Ming Che. "[FeIII(TF4DMAP)OTf] catalysed anti-Markovnikov oxidation of terminal aryl alkenes to aldehydes and transformation of methyl aryl tertiary amines to formamides with H2O2 as a terminal oxidant." Chem. Commun. 50, no. 84 (2014): 12669–72. http://dx.doi.org/10.1039/c4cc05972g.

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[Fe<sup>III</sup>(TF<sub>4</sub>DMAP)OTf] catalysed anti-Markovnikov oxidation of terminal aryl alkenes to aldehydes and the transformation of N-methyl aryl tertiary amines to formamides with H<sub>2</sub>O<sub>2</sub> as a terminal oxidant with moderate to good product yields.

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38

Xiao, Yumei, Zhanhu Sun, Hongchao Guo, and Ohyun Kwon. "Chiral phosphines in nucleophilic organocatalysis." Beilstein Journal of Organic Chemistry 10 (September 4, 2014): 2089–121. http://dx.doi.org/10.3762/bjoc.10.218.

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This review discusses the tertiary phosphines possessing various chiral skeletons that have been used in asymmetric nucleophilic organocatalytic reactions, including annulations of allenes, alkynes, and Morita–Baylis–Hillman (MBH) acetates, carbonates, and ketenes with activated alkenes and imines, allylic substitutions of MBH acetates and carbonates, Michael additions, γ-umpolung additions, and acylations of alcohols.

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39

Zhu, Chuanle, та Hengyuan Li. "Dual Roles of TBHP-Enabled Regioselective Hydroetherification of (Trifluoromethyl)alkenes with Boronic Acids: Access to α-Trifluoromethyl β-Aryloxy Tertiary Alcohols". Synthesis 53, № 16 (2021): 2881–88. http://dx.doi.org/10.1055/a-1481-2023.

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AbstractThe three-starting materials four-component reaction of (trifluoromethyl)alkenes, TBHP, and boronic acids is reported, delivering various useful α-trifluoromethyl-β-aryloxy tertiary alcohols in high yields and in an exclusively regioselective hydroetherification manner. TBHP serves as both the oxidant and nucleophile in this reaction, as well as the O-source of the products.

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40

Liu, Xin-Yuan, Xue-Fei Li, and Jin-Shun Lin. "Catalytic Radical Intramolecular Aminoperfluoroalkylation and Aminodifluoromethylation of Unactivated Alkenes with Fluoroalkylsulfonyl Chlorides." Synthesis 49, no. 18 (2017): 4213–20. http://dx.doi.org/10.1055/s-0036-1589044.

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The Cu(I)/phosphoric acid (PA) dual-catalyzed radical aminoperfluoroalkylation and aminodifluoromethylation of alkenes with commercially available fluoroalkylsulfonyl chlorides as the radical source is described. Functionalized α-tertiary pyrrolidines bearing four types of fluoroalkyl groups are obtained with moderate to excellent yields. The introduction of a Cu(I)/phosphoric acid dual catalytic system and the use of silver carbonate as a key additive to inhibit the side hydroamination reaction caused by the in situ generated HCl are crucial for the transformation.

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41

Kuyukina, Maria S., Irena B. Ivshina, Jim C. Philp, Nick Christofi, Sandra A. Dunbar, and Marina I. Ritchkova. "Recovery of Rhodococcus biosurfactants using methyl tertiary-butyl ether extraction." Journal of Microbiological Methods 46, no. 2 (2001): 149–56. http://dx.doi.org/10.1016/s0167-7012(01)00259-7.

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42

Anis, Raisa, Lesley Maclean, Lupiya Kimena, and Lesley Crichton. "Recovery facilities in a tertiary level hospital in Lusaka, Zambia." British Journal of Nursing 28, no. 9 (2019): 571–73. http://dx.doi.org/10.12968/bjon.2019.28.9.571.

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43

Yang, Guoju, Thomas J. Bauer, Gary L. Haller, and Eszter Baráth. "H-Transfer reactions of internal alkenes with tertiary amines as H-donors on carbon supported noble metals." Organic & Biomolecular Chemistry 16, no. 7 (2018): 1172–77. http://dx.doi.org/10.1039/c7ob02614e.

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44

Ibrahim, Abdulrahman D., Steven W. Entsminger, Lingyang Zhu, and Alison R. Fout. "A Highly Chemoselective Cobalt Catalyst for the Hydrosilylation of Alkenes using Tertiary Silanes and Hydrosiloxanes." ACS Catalysis 6, no. 6 (2016): 3589–93. http://dx.doi.org/10.1021/acscatal.6b01091.

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45

Kerchner, Hilary A., and John Montgomery. "Synthesis of Secondary and Tertiary Alkylboranes via Formal Hydroboration of Terminal and 1,1-Disubstituted Alkenes." Organic Letters 18, no. 21 (2016): 5760–63. http://dx.doi.org/10.1021/acs.orglett.6b03090.

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46

Gleave, D. Mark, Brad M. Savall, and William W. McWhorter. "A New Method for the Epoxidation of Alkenes in the Presence of Tertiary Amino Groups." Synthetic Communications 27, no. 14 (1997): 2425–32. http://dx.doi.org/10.1080/00397919708004106.

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47

Liu, Yang, and Liang Deng. "Mode of Activation of Cobalt(II) Amides for Catalytic Hydrosilylation of Alkenes with Tertiary Silanes." Journal of the American Chemical Society 139, no. 5 (2017): 1798–801. http://dx.doi.org/10.1021/jacs.6b12938.

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48

Salin, Alexey V., Albert R. Fatkhutdinov, Anton V. Il'in, and Fanuza G. Shamsutdinova. "Effect of Anchimeric Assistance in Addition Reaction of Bifunctional Tertiary Phosphines to Electron-Deficient Alkenes." International Journal of Chemical Kinetics 48, no. 3 (2016): 161–68. http://dx.doi.org/10.1002/kin.20981.

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49

Huang, Pengfei, Pan Wang, Shengchun Wang, Shan Tang, and Aiwen Lei. "Electrochemical oxidative [4 + 2] annulation of tertiary anilines and alkenes for the synthesis of tetrahydroquinolines." Green Chemistry 20, no. 21 (2018): 4870–74. http://dx.doi.org/10.1039/c8gc02463d.

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50

Iwaoka, Michio, and Shuji Tomoda. "Catalytic conversion of alkenes into allylic ethers and esters using diselenides having internal tertiary amines." Journal of the Chemical Society, Chemical Communications, no. 17 (1992): 1165. http://dx.doi.org/10.1039/c39920001165.

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