Статті в журналах з теми "Olefin oxidation"
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Perkins, Robert J., Hai-Chao Xu, John M. Campbell, and Kevin D. Moeller. "Anodic coupling of carboxylic acids to electron-rich double bonds: A surprising non-Kolbe pathway to lactones." Beilstein Journal of Organic Chemistry 9 (August 9, 2013): 1630–36. http://dx.doi.org/10.3762/bjoc.9.186.
Повний текст джерелаRayati, Saeed, Saeed Zakavi, Parisa Jafarzadeh, Omid Sadeghi, and Mostafa M. Amini. "Manganese meso-tetra-4-carboxyphenylporphyrin immobilized on MCM-41 as catalyst for oxidation of olefins with different oxygen donors in stoichiometric conditions." Journal of Porphyrins and Phthalocyanines 16, no. 03 (March 2012): 260–66. http://dx.doi.org/10.1142/s1088424612500307.
Повний текст джерелаLin, Bo-Lin, Jay A. Labinger, and John E. Bercaw. "Mechanistic investigations of bipyrimidine-promoted palladium-catalyzed allylic acetoxylation of olefins." Canadian Journal of Chemistry 87, no. 1 (January 1, 2009): 264–71. http://dx.doi.org/10.1139/v08-133.
Повний текст джерелаKřeček, Václav, Jiří Protiva, Miloš Buděšínský, Eva Klinotová, and Alois Vystrčil. "Preparation of C(18)-empiric 20,29,30-trinorlupane derivatives. 1H, 13C NMR and mass spectra." Collection of Czechoslovak Chemical Communications 51, no. 3 (1986): 621–35. http://dx.doi.org/10.1135/cccc19860621.
Повний текст джерелаSTINSON, STEPHEN. "IRON-CATALYZED OLEFIN OXIDATION." Chemical & Engineering News 79, no. 30 (July 23, 2001): 9. http://dx.doi.org/10.1021/cen-v079n030.p009.
Повний текст джерелаLorber, Christian. "[ONNO]-type amine bis(phenolate)-based vanadium catalysts for ethylene homo- and copolymerization." Pure and Applied Chemistry 81, no. 7 (June 30, 2009): 1205–15. http://dx.doi.org/10.1351/pac-con-08-08-05.
Повний текст джерелаHerrmann, Wolfgang A., Richard W. Fischer, and Dieter W. Marz. "Methyltrioxorhenium as Catalyst for Olefin Oxidation." Angewandte Chemie International Edition in English 30, no. 12 (December 1991): 1638–41. http://dx.doi.org/10.1002/anie.199116381.
Повний текст джерелаFukusumi, Takanori, Natsuki Takei, Yubi Tateno, Takuya Aoki, Ai Ando, Kouhei Kozakai, Hiroko Shima, et al. "Ene-thiol reaction of C3-vinylated chlorophyll derivatives in the presence of oxygen: synthesis of C3-formyl-chlorins under mild conditions." Journal of Porphyrins and Phthalocyanines 17, no. 12 (December 2013): 1188–95. http://dx.doi.org/10.1142/s1088424613500983.
Повний текст джерелаMa, Baochun, Wei Zhao, Fuming Zhang, Yingshuai Zhang, Songyun Wu, and Yong Ding. "A new halide-free efficient reaction-controlled phase-transfer catalyst based on silicotungstate of [(C18H37)2(CH3)2N]3[SiO4H(WO5)3] for olefin epoxidation, oxidation of sulfides and alcohols with hydrogen peroxide." RSC Adv. 4, no. 61 (2014): 32054–62. http://dx.doi.org/10.1039/c4ra04036h.
Повний текст джерелаPatrzałek, Michał, Aleksandra Zasada, Anna Kajetanowicz та Karol Grela. "Tandem Olefin Metathesis/α-Ketohydroxylation Revisited". Catalysts 11, № 6 (9 червня 2021): 719. http://dx.doi.org/10.3390/catal11060719.
Повний текст джерелаHerrmann, Wolfgang A., Richard W. Fischer, and Dieter W. Marz. "Methyltrioxorhenium als Katalysator für die Olefin-Oxidation." Angewandte Chemie 103, no. 12 (December 1991): 1706–9. http://dx.doi.org/10.1002/ange.19911031234.
Повний текст джерелаPilic, Branka, Dragoslav Stoiljkovic, Ivana Bakocevic, Slobodan Jovanovic, Davor Panic, and Ljiljana Korugic-Karasz. "The charge percolation mechanism and simulation of Ziegler-Natta polymerizations. Part III. Oxidation states of transition metals." Journal of the Serbian Chemical Society 71, no. 4 (2006): 357–72. http://dx.doi.org/10.2298/jsc0604357p.
Повний текст джерелаChen, Ruichao, Yuhong Ma, Changwen Zhao, Zhifeng Lin, Xing Zhu, Lihua Zhang, and Wantai Yang. "Construction of DNA microarrays on cyclic olefin copolymer surfaces using confined photocatalytic oxidation." RSC Adv. 4, no. 87 (2014): 46653–61. http://dx.doi.org/10.1039/c4ra07442d.
Повний текст джерелаLu, Yue, Han Zhang, Shaojun Liu, Chenglong Li, Lixiang Li, Baigang An, and Chengguo Sun. "Hemin-based conjugated effect synthesis of Fe–N/CNT catalysts for enhanced oxygen reduction." New Journal of Chemistry 45, no. 15 (2021): 6940–49. http://dx.doi.org/10.1039/d1nj00020a.
Повний текст джерелаBunchuay, T., R. Ketkaew, P. Chotmongkolsap, T. Chutimasakul, J. Kanarat, Y. Tantirungrotechai, and J. Tantirungrotechai. "Microwave-assisted one-pot functionalization of metal–organic framework MIL-53(Al)-NH2 with copper(ii) complexes and its application in olefin oxidation." Catalysis Science & Technology 7, no. 24 (2017): 6069–79. http://dx.doi.org/10.1039/c7cy01941f.
Повний текст джерелаPiola, Lorenzo, Fady Nahra, and Steven P. Nolan. "Olefin metathesis in air." Beilstein Journal of Organic Chemistry 11 (October 30, 2015): 2038–56. http://dx.doi.org/10.3762/bjoc.11.221.
Повний текст джерелаCarroll, AR, RW Read, and WC Taylor. "Intramolecular Oxidative Coupling of Aromatic Compounds. VII. A Convenient Synthesis of (±)-Deoxyschizandrin." Australian Journal of Chemistry 47, no. 8 (1994): 1579. http://dx.doi.org/10.1071/ch9941579.
Повний текст джерелаSingh, Adesh Kumar, Varsha Tiwari, Kunj Bihari Mishra, Surabhi Gupta, and Jeyakumar Kandasamy. "Urea–hydrogen peroxide prompted the selective and controlled oxidation of thioglycosides into sulfoxides and sulfones." Beilstein Journal of Organic Chemistry 13 (June 13, 2017): 1139–44. http://dx.doi.org/10.3762/bjoc.13.113.
Повний текст джерелаYi, Jigyoung, Hye Mi Ahn, Jong Ho Yoon, Cheal Kim, and Suk Joong Lee. "Preparation of a bispyridine based porous organic polymer as a new platform for Cu(ii) catalyst and its use in heterogeneous olefin epoxidation." New Journal of Chemistry 42, no. 17 (2018): 14067–70. http://dx.doi.org/10.1039/c8nj02214c.
Повний текст джерелаNunes, Carla D., Pedro D. Vaz, Vítor Félix, Luis F. Veiros, Tânia Moniz, Maria Rangel, Sara Realista, Ana C. Mourato, and Maria José Calhorda. "Vanadyl cationic complexes as catalysts in olefin oxidation." Dalton Transactions 44, no. 11 (2015): 5125–38. http://dx.doi.org/10.1039/c4dt03174a.
Повний текст джерелаGimferrer, Martí, Pedro Salvador, and Albert Poater. "Computational Monitoring of Oxidation States in Olefin Metathesis." Organometallics 38, no. 24 (December 4, 2019): 4585–92. http://dx.doi.org/10.1021/acs.organomet.9b00591.
Повний текст джерелаNunes, Carla D., and Maria José Calhorda. "Molybdenum(II) catalyst precursors in olefin oxidation reactions." Inorganica Chimica Acta 431 (May 2015): 122–31. http://dx.doi.org/10.1016/j.ica.2015.03.018.
Повний текст джерелаOLDENBURG, P., and L. QUEJR. "Bio-inspired nonheme iron catalysts for olefin oxidation." Catalysis Today 117, no. 1-3 (September 30, 2006): 15–21. http://dx.doi.org/10.1016/j.cattod.2006.05.022.
Повний текст джерелаGrate, John H., David R. Hamm, and Suresh Mahajan. "Palladium and phosphomolybdovanadate catalyzed olefin oxidation to carbonyls." Molecular Engineering 3, no. 1-3 (1993): 205–29. http://dx.doi.org/10.1007/bf00999634.
Повний текст джерелаOgoshi, Hisanobu, Yasuhiko Suzuki, and Yasuhisa Kuroda. "Olefin Oxidation Catalyzed by Electron Deficient Metallo-Porphyrin." Chemistry Letters 20, no. 9 (September 1991): 1547–50. http://dx.doi.org/10.1246/cl.1991.1547.
Повний текст джерелаWang, Jian-Cheng, Yu-Hong Hu, Gong-Jun Chen, and Yu-Bin Dong. "Cu(ii)/Cu(0)@UiO-66-NH2: base metal@MOFs as heterogeneous catalysts for olefin oxidation and reduction." Chemical Communications 52, no. 89 (2016): 13116–19. http://dx.doi.org/10.1039/c6cc06076e.
Повний текст джерелаSong, Xiaojing, Yan Yan, Yanning Wang, Dianwen Hu, Lina Xiao, Jiehui Yu, Wenxiang Zhang, and Mingjun Jia. "Hybrid compounds assembled from copper-triazole complexes and phosphomolybdic acid as advanced catalysts for the oxidation of olefins with oxygen." Dalton Transactions 46, no. 47 (2017): 16655–62. http://dx.doi.org/10.1039/c7dt03198j.
Повний текст джерелаIyer, Shyam R., Maedeh Moshref Javadi, Yan Feng, Min Young Hyun, Williamson N. Oloo, Cheal Kim, and Lawrence Que. "A chameleon catalyst for nonheme iron-promoted olefin oxidation." Chem. Commun. 50, no. 89 (September 17, 2014): 13777–80. http://dx.doi.org/10.1039/c4cc06164k.
Повний текст джерелаSaraiva, Marta S., Cristina I. Fernandes, Teresa G. Nunes, Maria José Calhorda, and Carla D. Nunes. "Pore size matters! Helical heterogeneous catalysts in olefin oxidation." Applied Catalysis A: General 504 (September 2015): 328–37. http://dx.doi.org/10.1016/j.apcata.2015.01.040.
Повний текст джерелаMansour, E. M. K., P. Maillard, P. Krausz, S. Gaspard, and C. Giannotti. "Photochemically induced olefin oxidation by titanyl and vanadyl porphyrins." Journal of Molecular Catalysis 41, no. 3 (August 1987): 361–66. http://dx.doi.org/10.1016/0304-5102(87)80113-x.
Повний текст джерелаZhang, Baoan, Nengsheng Liu, Qingsong Lin, and Dai Jin. "The effects of Mo oxidation states on olefin metathesis." Journal of Molecular Catalysis 65, no. 1-2 (March 1991): 15–28. http://dx.doi.org/10.1016/0304-5102(91)85078-g.
Повний текст джерелаDauth, Alexander, and Jennifer A. Love. "Preparation of 2-Azarhodacyclobutanes by Rhodium(I)-Olefin Oxidation." Angewandte Chemie International Edition 51, no. 15 (February 28, 2012): 3634–37. http://dx.doi.org/10.1002/anie.201107669.
Повний текст джерелаWu, Nan, Zhi-Min Zong, Yi-Wei Fei, Jun Ma та Feng Guo. "Thermal oxidation stability of poly-α -olefin lubricating oil". Asia-Pacific Journal of Chemical Engineering 12, № 5 (вересень 2017): 813–17. http://dx.doi.org/10.1002/apj.2121.
Повний текст джерелаMuñiz, Kilian. "Electronic Effects in Olefin Oxidation by Imidoosmium(VIII) Compounds." European Journal of Organic Chemistry 2004, no. 10 (May 2004): 2243–52. http://dx.doi.org/10.1002/ejoc.200300774.
Повний текст джерелаDauth, Alexander, and Jennifer A. Love. "Preparation of 2-Azarhodacyclobutanes by Rhodium(I)-Olefin Oxidation." Angewandte Chemie 124, no. 15 (February 28, 2012): 3694–97. http://dx.doi.org/10.1002/ange.201107669.
Повний текст джерелаPilić, B., D. Stoiljković, I. Bakočević, S. Jovanović, D. Panić, and Lj Korugić-Karasz. "Polymer Structure Prediction by Computer Simulation of Ziegler-Natta Polymerization Based on Charge Percolation Mechanism." Materials Science Forum 518 (July 2006): 381–86. http://dx.doi.org/10.4028/www.scientific.net/msf.518.381.
Повний текст джерелаMa, Yuefeng, Jian Xu, Xiangqiong Zeng, Haizhen Jiang, and Jiusheng Li. "Preparation and performance evaluation of mPAO8 using olefin from coal as raw material." Industrial Lubrication and Tribology 69, no. 5 (September 4, 2017): 678–82. http://dx.doi.org/10.1108/ilt-03-2016-0049.
Повний текст джерелаChen, Jian, Mengjing Zhu, Fuwei Xiang, Junfeng Li, Hongjun Yang, and Zhipeng Mao. "Research Progress on Microreactor Technology in Oxidation Reactions." Current Organic Chemistry 25, no. 10 (June 1, 2021): 1235–45. http://dx.doi.org/10.2174/1385272825666210319092545.
Повний текст джерелаParyzek, Zozislaw, and Jacek Martynow. "Tetracyclic triterpenes. X. Solvent effect in reactions of tetrasubstituted triterpenoidal olefins with ozone. An allylic oxidation." Canadian Journal of Chemistry 66, no. 9 (September 1, 1988): 2130–36. http://dx.doi.org/10.1139/v88-338.
Повний текст джерелаQuiller, Ryan G, Xiaoying Liu, and Cynthia M Friend. "Mechanistic Insights into Selectivity Control for Heterogeneous Olefin Oxidation: Styrene Oxidation on Au(111)." Chemistry - An Asian Journal 5, no. 1 (January 4, 2010): 78–86. http://dx.doi.org/10.1002/asia.200900399.
Повний текст джерелаSales, Rita N., Samantha K. Callear, Pedro D. Vaz, and Carla D. Nunes. "Substrate–Solvent Crosstalk—Effects on Reaction Kinetics and Product Selectivity in Olefin Oxidation Catalysis." Chemistry 3, no. 3 (July 19, 2021): 753–64. http://dx.doi.org/10.3390/chemistry3030054.
Повний текст джерелаFajkoš, Jan, та Jiří Joska. "Solvolytic rearrangements in 4β,5-cyclopropano-5β-androstane-3β,17β,19-triol 3-acetate 17-benzoate 19-p-toluenesulfonate". Collection of Czechoslovak Chemical Communications 54, № 3 (1989): 751–59. http://dx.doi.org/10.1135/cccc19890751.
Повний текст джерелаPliss, E. M., V. A. Machtin, I. V. Tikhonov, A. V. Sirik, A. M. Grobov, and O. A. Yasinsky. "Catalytic inhibition of olefin oxidation with Mn and Cu compounds." Russian Chemical Bulletin 70, no. 10 (October 2021): 2027–30. http://dx.doi.org/10.1007/s11172-021-3312-2.
Повний текст джерелаGovindan, S. V., and P. L. Fuchs. "Regiospecific quassinoidal A-ring synthesis via an olefin oxidation strategy." Journal of Organic Chemistry 53, no. 11 (May 1988): 2593–97. http://dx.doi.org/10.1021/jo00246a036.
Повний текст джерелаMORI, Tomonori, Motowo YAMAGUCHI, and Takamichi YAMAGISHI. "Hydrogen Peroxide Oxidation of Olefin Catalyzed by Polyaminopolycarboxylatoruthenium(III) Complexes." NIPPON KAGAKU KAISHI, no. 5 (1997): 329–34. http://dx.doi.org/10.1246/nikkashi.1997.329.
Повний текст джерелаBirnbaum, Eva R., Jay A. Labinger, John E. Bercaw, and Harry B. Gray. "Catalysis of aerobic olefin oxidation by a ruthenium perhaloporphyrin complex." Inorganica Chimica Acta 270, no. 1-2 (April 1998): 433–39. http://dx.doi.org/10.1016/s0020-1693(97)06000-3.
Повний текст джерелаKato, Tadahiro, Toshifumi Hirukawa, and Kohji Namiki. "Selective terminal olefin oxidation of n-3 polyunsaturated fatty acids." Tetrahedron Letters 33, no. 11 (March 1992): 1475–78. http://dx.doi.org/10.1016/s0040-4039(00)91651-4.
Повний текст джерелаBrown, John M., Robert A. John, and Andrew R. Lucy. "Observations on olefin oxidation by neutral and cationic phosphineiridium complexes." Journal of Organometallic Chemistry 279, no. 1-2 (January 1985): 245–57. http://dx.doi.org/10.1016/0022-328x(85)87022-4.
Повний текст джерелаNair, Vipin A., M. M. Suni та K. Sreekumar. "Polystyrene-supported β-diketone-linked palladium complexes for olefin oxidation". Designed Monomers and Polymers 6, № 1 (січень 2003): 81–89. http://dx.doi.org/10.1163/156855503321127556.
Повний текст джерелаPáez-Mozo, E., N. Gabriunas, R. Maggi, D. Acosta, P. Ruiz, and B. Delmon. "Selective olefin oxidation with cobalt phthalocyanine encapsulated in Y-zeolite." Journal of Molecular Catalysis 91, no. 2 (July 1994): 251–58. http://dx.doi.org/10.1016/0304-5102(94)00027-1.
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