Log in

Relevant bibliographies by topics / Biomimetic oxidation / Journal articles

To see the other types of publications on this topic, follow the link: Biomimetic oxidation.

Journal articles on the topic 'Biomimetic oxidation'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Biomimetic oxidation.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Hong, Yiming, Tiantian Fang, Meichao Li, et al. "2,3-Dichloro-5,6-dicyano-1,4-benzoquinone-catalyzed aerobic oxidation reactions via multistep electron transfers with iron(ii) phthalocyanine as an electron-transfer mediator." RSC Advances 6, no. 57 (2016): 51908–13. http://dx.doi.org/10.1039/c6ra08921f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Murray, Alexander T., Pascal Matton, Nathan W. G. Fairhurst, Matthew P. John, and David R. Carbery. "Biomimetic Flavin-Catalyzed Aldehyde Oxidation." Organic Letters 14, no. 14 (2012): 3656–59. http://dx.doi.org/10.1021/ol301496m.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Smolinka, Kai, and Berthold Göber. "Biomimetic Oxidation of Denaverine Hydrochloride." European Journal of Organic Chemistry 1999, no. 3 (1999): 679–83. http://dx.doi.org/10.1002/(sici)1099-0690(199903)1999:3<679::aid-ejoc679>3.0.co;2-w.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

S., M. S. CHAUHAN. "Biomimetic Oxidation of Organic Substrates by Chemical Models of Cytochrome P-450 and related Heme Monooxygenases." Journal of Indian Chemical Society Vol. 73, Dec 1996 (1996): 637–45. https://doi.org/10.5281/zenodo.6075469.

Full text

Abstract:

Department of Chemistry, University of Delhi, Delhi-110 007 <em>Manuscript received 20 September 1995</em> Biomimetic Oxidation of Organic Substrates by Chemical Models of Cytochrome P-450 and related Heme Monooxygenases.

APA, Harvard, Vancouver, ISO, and other styles

5

Simões, Mário M. Q., Cláudia M. B. Neves, Sónia M. G. Pires, M. Graça P. M. S. Neves, and José A. S. Cavaleiro. "Mimicking P450 processes and the use of metalloporphyrins." Pure and Applied Chemistry 85, no. 8 (2013): 1671–81. http://dx.doi.org/10.1351/pac-con-12-11-15.

Full text

Abstract:

Metalloporphyrins (MPs) are known to catalyze in vitro a broad range of cytochrome P450-mediated reactions occurring in vivo. Most of the biomimetic research using MPs in oxidative catalysis has been directed towards the oxidation of organic compounds presenting significant reactivity features in one functional group. Much less effort has been made to imitate the oxidation of more complex molecules, with a range of functionalities, such as drugs or other xenobiotics. By varying the structure of the porphyrin, the metal ion, the oxidant, and the reaction conditions, it is possible to modulate t

APA, Harvard, Vancouver, ISO, and other styles

6

Aghamammadova, S. A. "MECHANISM OF BIOMIMETIC OXIDATION OF CYCLOHEXANE TO CYCLOHEXANONE BY HYDROGEN PEROXIDE." Azerbaijan Chemical Journal, no. 1 (April 9, 2021): 61–66. http://dx.doi.org/10.32737/0005-2531-2021-1-61-66.

Full text

Abstract:

The process of gas-phase oxidation of cyclohexane was studied in the presence of a heterogeneous biomimetic catalyst (per-FTPhPFe(III)OH/Al2O3), at 130–2500C, in which high yields of cyclohexanone and cyclohexanol were obtained up to 25.2% with a selectivity of ~80% at a cyclohexane conversion of 34%. The mechanism of the conversion of cyclohexane to cyclohexanone has been studied in detail, and the coherently synchronized character of the reaction proceeding is shown

APA, Harvard, Vancouver, ISO, and other styles

7

Lavilla, Rodolfo, Francisco Gullón, Xavier Barón, and Joan Bosch. "Non-biomimetic oxidation of 1,4-dihydropyridines." Chemical Communications, no. 2 (1997): 213–14. http://dx.doi.org/10.1039/a606919c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Karasevich, Elena I., Vera S. Kulikova, Aleksandr E. Shilov, and Al'bert A. Shteinman. "Biomimetic alkane oxidation involving metal complexes." Russian Chemical Reviews 67, no. 4 (1998): 335–55. http://dx.doi.org/10.1070/rc1998v067n04abeh000315.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Santos, Joicy Santamalvina dos, Vinícius Palaretti, André Luiz de Faria, Eduardo José Crevelin, Luiz Alberto Beraldo de Moraes, and Marilda das Dores Assis. "Biomimetic simazine oxidation catalyzed by metalloporphyrins." Applied Catalysis A: General 408, no. 1-2 (2011): 163–70. http://dx.doi.org/10.1016/j.apcata.2011.09.023.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Einig, Till, Gerhard Görlitz, and Bernd Neidhart. "Biomimetic oxidation of plant protecting agents." Fresenius Journal of Analytical Chemistry 355, no. 1 (1996): 71–77. http://dx.doi.org/10.1007/s0021663550071.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Shteinman, A. A. "Biomimetic alkane oxidation: Modelling methane monooxygenase." Journal of Inorganic Biochemistry 59, no. 2-3 (1995): 408. http://dx.doi.org/10.1016/0162-0134(95)97506-l.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Karakhanov, E. A., A. L. Maksimov, and E. A. Ivanova. "Supramolecular catalytic systems in biomimetic oxidation." Russian Chemical Bulletin 56, no. 4 (2007): 621–30. http://dx.doi.org/10.1007/s11172-007-0102-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Karasevich, E. I. "ChemInform Abstract: Biomimetic Oxidation of Alkanes." ChemInform 42, no. 39 (2011): no. http://dx.doi.org/10.1002/chin.201139261.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Hage, Ronald. "Oxidation catalysis by biomimetic manganese complexes." Recueil des Travaux Chimiques des Pays-Bas 115, no. 9 (2010): 385–95. http://dx.doi.org/10.1002/recl.19961150902.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Mammadova, U. V., I. T. Nagieva, L. M. Gasanova, and T. M. Nagiev. "KINETICS OF COHERENT-SYNCHRONIZED PEROXIDASE OXIDATION OF ETHYL ALCOHOL TO ACETALDEHYDE ON HETEROGENIZED BIOMIMETIC CATALYSTS." Azerbaijan Chemical Journal, no. 3 (September 22, 2022): 12–20. http://dx.doi.org/10.32737/0005-2531-2022-3-12-20.

Full text

Abstract:

The peroxidase activity of the synthesized heterogeneous biomimetic catalysts, PPFe3+OH/Al2O3, TPhPFe3+OH/Al2O3 and per-FTPhPFe3+OH/Al2O3 in the reaction of ethyl alcohol oxidation to acetaldehyde with hydrogen peroxide has been studied, which showed high catalase activity and unique resistance to the action of highly active intermediate reaction products. As a result of studying the kinetic regularities of the selective biomimetic oxidation of ethyl alcohol with hydrogen peroxide, a coherent-synchronized nature of the reaction was established, consisting of two: 1) catalase and 2) peroxidase

APA, Harvard, Vancouver, ISO, and other styles

16

U., V. Mammadova* I. T. Nagieva L. M. Gasanova T. M. Nagiev. "MACROKINETIC COHERENCE OF GAS-PHASE ETHYLENE MONOOXIDATION REACTION BY HYDROGEN PEROXIDE." INTERNATIONAL JOURNAL OF ENGINEERING SCIENCES & RESEARCH TECHNOLOGY 5, no. 12 (2016): 185–93. https://doi.org/10.5281/zenodo.192566.

Full text

Abstract:

The gas-phase monooxidation of ethylene by hydrogen peroxide on a biomimetic heterogeneous catalyst, perfluorinated iron (III) tetraphenylporphyrin, deposited on alumina (per-FTPhPFe3+OH/Al2O3)was studied under comparatively mild conditions. The biomimetic oxidation of ethylene with hydrogen peroxide was shown to be coherently synchronized with the decomposition of H2O2. Depending on reaction medium conditions, one of two desired products was formed, either ethanol or acetaldehyde. The probable mechanism of ethylene transformation was studied. A kinetic model that fits the experimental data is

APA, Harvard, Vancouver, ISO, and other styles

17

Iida, Hiroki, Marina Oka, and Ryo Kozako. "Green Aerobic Oxidation of Thiols to Disulfides by Flavin–Iodine Coupled Organocatalysis." Synlett 32, no. 12 (2021): 1227–30. http://dx.doi.org/10.1055/a-1520-9916.

Full text

Abstract:

AbstractCoupled catalysis using a riboflavin-derived organocatalyst and molecular iodine successfully promoted the aerobic oxidation of thiols to disulfides under metal-free mild conditions. The activation of molecular oxygen occurred smoothly at room temperature through the transfer of electrons from the iodine catalyst to the biomimetic flavin catalyst, forming the basis for a green oxidative synthesis of disulfides from thiols.

APA, Harvard, Vancouver, ISO, and other styles

18

Ding, Yuxiao, Pengfei Zhang, Hailong Xiong, et al. "Tuning regioselective oxidation toward phenol via atomically dispersed iron sites on carbon." Green Chemistry 22, no. 18 (2020): 6025–32. http://dx.doi.org/10.1039/d0gc01717e.

Full text

Abstract:

Inspired by iron enzymes exhibiting a high level of selectivity in hydrocarbon oxidation reactions, a biomimetic iron-based heterogeneous catalyst is developed to achieve remarkable activity and unprecedented selectivity toward phenol oxidation.

APA, Harvard, Vancouver, ISO, and other styles

19

Melo, Andrea J. B., Yassuko Iamamoto, Ana Paula J. Maestrin, et al. "Biomimetic oxidation of praziquantel catalysed by metalloporphyrins." Journal of Molecular Catalysis A: Chemical 226, no. 1 (2005): 23–31. http://dx.doi.org/10.1016/j.molcata.2004.09.015.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Berkessel, Albrecht. "Biomimetic and organocatalytic approaches to oxidation catalysis." Pure and Applied Chemistry 77, no. 7 (2005): 1277–84. http://dx.doi.org/10.1351/pac200577071277.

Full text

Abstract:

The lecture summarized our recent work in the fields of (i) catalytic asymmetric epoxidation and cyclopropanation, (ii) C–C coupling reactions, and (iii) dynamic kinetic resolution (DKR). The first section describes the use of chiral Ru-porphyrins as catalysts for the asymmetric epoxidation and cyclopropanation of nonfunctionalized olefins, and of peptides and alkaloid-based phase-transfer catalysts for the asymmetric epoxidation of enones. The second section highlights the application of the DIANANE-salen ligands (DIANANE: endo,endo-2,5-diamino-norbornane) to the asymmetric Nozaki–Hiyama–Kish

APA, Harvard, Vancouver, ISO, and other styles

21

Murray, Alexander T., Pascal Matton, Nathan W. G. Fairhurst, Matthew P. John, and David R. Carbery. "ChemInform Abstract: Biomimetic Flavin-Catalyzed Aldehyde Oxidation." ChemInform 43, no. 46 (2012): no. http://dx.doi.org/10.1002/chin.201246074.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Endo, Yoshinori, and Jan-E. Bäckvall. "Aerobic Lactonization of Diols by Biomimetic Oxidation." Chemistry - A European Journal 17, no. 45 (2011): 12596–601. http://dx.doi.org/10.1002/chem.201102168.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Golime, Gangadhararao, Ganganna Bogonda, Hun Young Kim, and Kyungsoo Oh. "Biomimetic Oxidative Deamination Catalysis via ortho-Naphthoquinone-Catalyzed Aerobic Oxidation Strategy." ACS Catalysis 8, no. 6 (2018): 4986–90. http://dx.doi.org/10.1021/acscatal.8b00992.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Zografos, Alexandros, and Marina Petsi. "Advances in Catalytic Aerobic Oxidations by Activation of Dioxygen-Monooxygenase Enzymes and Biomimetics." Synthesis 50, no. 24 (2018): 4715–45. http://dx.doi.org/10.1055/s-0037-1610297.

Full text

Abstract:

Monooxygenases are not only some of the most versatile machineries in our lives, but also some of the most explored enzymes in modern organic synthesis. They provide knowledge and inspiration on how the most abandoned oxidant, dioxygen, can be activated and utilized to deliver selective oxidations. This review presents an outline in the mechanisms that Nature uses to succeed in these processes and recent indicative examples on how chemists use this knowledge to develop selective oxidation protocols based on dioxygen as the terminal oxidant.1 Introduction2 Monooxygenases2.1 Metal-Based Monooxyg

APA, Harvard, Vancouver, ISO, and other styles

25

Maachou, Lahcene, Kun Qi, Eddy Petit, et al. "Biomimetic electro-oxidation of alkyl sulfides from exfoliated molybdenum disulfide nanosheets." Journal of Materials Chemistry A 8, no. 47 (2020): 25053–60. http://dx.doi.org/10.1039/d0ta09045j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Podder, Nirmalya, and Sukanta Mandal. "Aerobic oxidation of 2-aminophenol catalysed by a series of mononuclear copper(ii) complexes: phenoxazinone synthase-like activity and mechanistic study." New Journal of Chemistry 44, no. 29 (2020): 12793–805. http://dx.doi.org/10.1039/d0nj02558e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Prathap, Kaniraj Jeya, and Galia Maayan. "Metallopeptoids as efficient biomimetic catalysts." Chemical Communications 51, no. 55 (2015): 11096–99. http://dx.doi.org/10.1039/c5cc04266f.

Full text

Abstract:

Metallopeptoid catalysts incorporating phenanthroline–copper and TEMPO, and at least one non-catalytic group perform in the oxidation of various benzylic, allylic and aliphatic primary alcohols with a TON of up to 16 times higher than a mixture of the two catalytic groups or the peptoid dimer that is lacking the non-catalytic group.

APA, Harvard, Vancouver, ISO, and other styles

28

Moghadam, Majid, Masoud Nasr-Esfahani, Shahram Tangestaninejad, Valiollah Mirkhani, and Mohammad Ali Zolfigol. "Biomimetic aromatization of Hantzsch 1,4-dihydropyridines with sodium periodate catalyzed by a new polystyrene-bound manganese porphyrin." Canadian Journal of Chemistry 84, no. 1 (2006): 1–4. http://dx.doi.org/10.1139/v05-255.

Full text

Abstract:

Efficient oxidation of Hantzsch 1,4-dihydropyridines with sodium periodate catalyzed by a polystyrene-bound manganese(III) porphyrin is reported. This catalyst shows high activity in the oxidation of various 1,4-dihydropyridines at room temperature. This heterogeneous catalyst can be reused five times without significant loss of its activity.Key words: biomimetic oxidation, supported metalloporphyrin, periodate, 1,4-dihydropyridine.

APA, Harvard, Vancouver, ISO, and other styles

29

Zhang, Lina, Junying Chen, Ting Fan, Kui Shen, Miao Jiang та Yingwei Li. "A high-valent di-μ-oxo dimanganese complex covalently anchored in a metal–organic framework as a highly efficient and recoverable water oxidation catalyst". Chemical Communications 54, № 33 (2018): 4188–91. http://dx.doi.org/10.1039/c8cc00258d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Perrone, Maria L., Elena Salvadeo, Eliana Lo Presti, et al. "A dinuclear biomimetic Cu complex derived from l-histidine: synthesis and stereoselective oxidations." Dalton Transactions 46, no. 12 (2017): 4018–29. http://dx.doi.org/10.1039/c7dt00147a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Marais, Lindie, and Andrew John Swarts. "Biomimetic Cu/Nitroxyl Catalyst Systems for Selective Alcohol Oxidation." Catalysts 9, no. 5 (2019): 395. http://dx.doi.org/10.3390/catal9050395.

Full text

Abstract:

The oxidation of alcohols to the corresponding carbonyl products is an important organic transformation and the products are used in a variety of applications. The development of catalytic methods for selective alcohol oxidation have garnered significant attention in an attempt to find a more sustainable method without any limitations. Copper, in combination with 2,2,6,6-tetramethyl-1-piperidine N-oxyl (TEMPO) and supported by organic ligands, have emerged as the most effective catalysts for selective alcohol oxidation and these catalyst systems are frequently compared to galactose oxidase (GO

APA, Harvard, Vancouver, ISO, and other styles

32

Meng, Xu, Chaoying Yu, Gexin Chen, and Peiqing Zhao. "Heterogeneous biomimetic aerobic synthesis of 3-iodoimidazo[1,2-a]pyridines via CuOx/OMS-2-catalyzed tandem cyclization/iodination and their late-stage functionalization." Catalysis Science & Technology 5, no. 1 (2015): 372–79. http://dx.doi.org/10.1039/c4cy00919c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

da Silva, Vinicius Santos, Warleson Cândido dos Santos Vieira, Alexandre Moreira Meireles, et al. "Biomimetic oxidation of cyclic and linear alkanes: high alcohol selectivity promoted by a novel manganese porphyrin catalyst." New Journal of Chemistry 41, no. 3 (2017): 997–1006. http://dx.doi.org/10.1039/c6nj03072f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Zanatta, L. D., I. A. Barbosa, F. B. Zanardi, et al. "Hydrocarbon oxidation by iron-porphyrin immobilized on SBA-15 as biomimetic catalyst: role of silica surface." RSC Advances 6, no. 106 (2016): 104886–96. http://dx.doi.org/10.1039/c6ra18395f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Saghian, M., S. Dehghanpour, and M. Sharbatdaran. "“Ship in a bottle” Porph@MOMs as highly efficient catalysts for selective controllable oxidation and insights into different mechanisms in heterogeneous and homogeneous environments." New Journal of Chemistry 42, no. 15 (2018): 12872–81. http://dx.doi.org/10.1039/c8nj00315g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Weber, Georges, Thierry Charitat, Maurício S. Baptista, et al. "Lipid oxidation induces structural changes in biomimetic membranes." Soft Matter 10, no. 24 (2014): 4241. http://dx.doi.org/10.1039/c3sm52740a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Wu, He, Yong Wang, Guangguang Yang, Karuppu Selvaraj, and Gang Chen. "Biomimetic oxidation of tetracycline and derivatives at C11a." Tetrahedron Letters 154 (January 2025): 155366. http://dx.doi.org/10.1016/j.tetlet.2024.155366.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Shelnutt, J. A., and D. E. Trudell. "Photochemically-driven biomimetic oxidation of alkanes and olefins." Tetrahedron Letters 30, no. 39 (1989): 5231–34. http://dx.doi.org/10.1016/s0040-4039(01)93749-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Linhares, Margarida, Susana L. H. Rebelo, Mário M. Q. Simões, et al. "Biomimetic oxidation of indole by Mn(III)porphyrins." Applied Catalysis A: General 470 (January 2014): 427–33. http://dx.doi.org/10.1016/j.apcata.2013.11.023.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Hino, Fumio, and David Dolphin. "The biomimetic oxidation of dieldrin using polyhalogenated metalloporphyrins." Chemical Communications, no. 7 (1999): 629–30. http://dx.doi.org/10.1039/a809080g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Mansuy, D. "Biomimetic catalysts for selective oxidation in organic chemistry." Pure and Applied Chemistry 62, no. 4 (1990): 741–46. http://dx.doi.org/10.1351/pac199062040741.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

KARASEVICH, E. I., V. S. KULIKOVA, A. E. SHILOV, and A. A. SHTEINMAN. "ChemInform Abstract: Biomimetic Alkane Oxidation Involving Metal Complexes." ChemInform 29, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199836342.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

LAVILLA, R., F. GULLON, X. BARON, and J. BOSCH. "ChemInform Abstract: Non-Biomimetic Oxidation of 1,4-Dihydropyridines." ChemInform 28, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.199723176.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Guðmundsson, Arnar, Kim Elisabeth Schlipköter, and Jan‐E Bäckvall. "Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols." Angewandte Chemie 132, no. 13 (2020): 5441–44. http://dx.doi.org/10.1002/ange.202000054.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Guðmundsson, Arnar, Kim Elisabeth Schlipköter, and Jan‐E Bäckvall. "Iron(II)‐Catalyzed Biomimetic Aerobic Oxidation of Alcohols." Angewandte Chemie International Edition 59, no. 13 (2020): 5403–6. http://dx.doi.org/10.1002/anie.202000054.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Babu, Beneesh P., Yoshinori Endo, and Jan-E. Bäckvall. "Biomimetic Aerobic Oxidation of Amino Alcohols to Lactams." Chemistry - A European Journal 18, no. 37 (2012): 11524–27. http://dx.doi.org/10.1002/chem.201202080.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

HAGE, R. "ChemInform Abstract: Oxidation Catalysis by Biomimetic Manganese Complexes." ChemInform 28, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.199705320.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Ogawa, Narihito, Sei Furukawa, Yuya Kosugi, Takayuki Takazawa, and Nobuhiro Kanomata. "Biomimetic systems involving sequential redox reactions in glycolysis – the sulfur effect." Chemical Communications 56, no. 85 (2020): 12917–20. http://dx.doi.org/10.1039/d0cc05185c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Nahmatova, G. Ch, L. M. Gasanova, and T. M. Nagiev. "MECHANISM AND KINETICS OF DIRECT OXIDATION OF METHANE TO METHANOL BY HYDROGEN PEROXIDE ON A BIOMIMETIC CATALYST IN THE CONTEXT OF COHERENTLY SYNCHRONIZED REACTIONS." Azerbaijan Chemical Journal, no. 3 (June 24, 2025): 54–62. https://doi.org/10.32737/0005-2531-2025-3-54-62.

Full text

Abstract:

The biomimetic catalyst penta-FTPhPFe(III)OH/Al2O3 was synthesized by adsorption of the active complex FTPhPFe(III)OH on Al2O3 from a solution in dimethylformamide The active complex concentration relative to the Al2O3 mass was 0.64 mg/g. Activity of penta- FTPhPFe(III)/Al2O3 biomimetic catalyst in the reaction of methane direct conversion into methanol by green oxidant hydrogen peroxide was studied at the t=150-350°C and atmospheric pressure, where methanol yield was 19.2% with methane conversion of 28%. The kinetic investigation of methane biomimetic monooxidation reaction with hydrogen pero

APA, Harvard, Vancouver, ISO, and other styles

50

Carail, Michel, and Catherine Caris-Veyrat. "Carotenoid oxidation products: From villain to saviour?" Pure and Applied Chemistry 78, no. 8 (2006): 1493–503. http://dx.doi.org/10.1351/pac200678081493.

Full text

Abstract:

Carotenoid oxidation products have various structures, among which epoxides and apo- or seco-carotenoids are the two main families. Although both these compound types are widely found in the natural world, the sensitivity of carotenoids to oxidation means they can also be an unwanted presence in in vitro assays. On the other hand, carotenoid oxidation products have also provided chemists with useful chemical tools for the structural identification of carotenoids, and in the natural world they are important biological mediators for plants and animals. In vitro, carotenoid oxidation products hav

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!