Relevant bibliographies by topics / Oxidative coupling of phenols

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Oxidative coupling of phenols'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Oxidative coupling of phenols.'

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.

Journal articles on the topic "Oxidative coupling of phenols"

1

Kidwai, Mazaahir, Arti Jain, Abha Sharma, and Ramesh Chander Kuhad. "Ecofriendly approach for detection of phenols in water using laccase from different fungi." Water Science and Technology 66, no. 2 (2012): 385–93. http://dx.doi.org/10.2166/wst.2012.198.

Full text
Abstract:
Laccase-initiated oxidative coupling reactions of phenol and its derivatives with 4-aminoantipyrene using air as an oxidant has been investigated. The oxidation reaction of phenols and 4-aminoantipyrene is getting a lot of attention due to environmental concerns. Oxidation of simple phenol and 4-aminoantipyrene as a benchmark reaction enabled us to rank the relative oxidation ability of various laccases. Among the laccases tested, laccase from Pycnoporus cinnabarinus successfully yielded 72% antipyrilquinoneimine dye. The present method can also be used to determine p-substituted phenols and c
APA, Harvard, Vancouver, ISO, and other styles
2

He, Zhen, Gregory J. P. Perry, and David J. Procter. "Sulfoxide-mediated oxidative cross-coupling of phenols." Chemical Science 11, no. 7 (2020): 2001–5. http://dx.doi.org/10.1039/c9sc05668h.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Takizawa, Shinobu, Junpei Kodera, Yasushi Yoshida, et al. "Enantioselective oxidative-coupling of polycyclic phenols." Tetrahedron 70, no. 9 (2014): 1786–93. http://dx.doi.org/10.1016/j.tet.2014.01.017.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Dec, Jerzy, and Jean Marc Bollag. "Dehalogenation of Chlorinated Phenols during Oxidative Coupling." Environmental Science & Technology 28, no. 3 (1994): 484–90. http://dx.doi.org/10.1021/es00052a022.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Kang, Houng, Young Eun Lee, Peddiahgari Vasu Govardhana Reddy, et al. "Asymmetric Oxidative Coupling of Phenols and Hydroxycarbazoles." Organic Letters 19, no. 20 (2017): 5505–8. http://dx.doi.org/10.1021/acs.orglett.7b02552.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Hay, Allan S. "Polymerization by oxidative coupling. II. Oxidation of 2,6-disubstituted phenols." Journal of Polymer Science Part A: Polymer Chemistry 34, no. 8 (1996): 1373–83. http://dx.doi.org/10.1002/pola.1996.829.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Jiang, Qing, Wenbing Sheng, Mi Tian, Jie Tang, and Cancheng Guo. "Cobalt(II)-Porphyrin-Catalyzed Aerobic Oxidation: Oxidative Coupling of Phenols." European Journal of Organic Chemistry 2013, no. 10 (2013): 1861–66. http://dx.doi.org/10.1002/ejoc.201201595.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Truchan, Nadina, Christian Jandl, Alexander Pöthig, Stefan Breitenlechner, and Thorsten Bach. "Access to Biphenyls by Palladium-Catalyzed Oxidative Coupling of Phenyl Carbamates and Phenols." Synthesis 51, no. 16 (2019): 3060–76. http://dx.doi.org/10.1055/s-0037-1611482.

Full text
Abstract:
The oxidative cross-coupling of phenols (3 equiv) to various substituted phenyl N,N-diethylcarbamates was explored with a variety of substrates. Pd(OAc)2 was employed as the catalyst (20 mol%) and K2S2O8 as the stoichiometric oxidant in trifluoroacetic acid as the solvent (50 °C, 2 h). Carbamates without or with a substituent on the phenyl ring (Me, Ph, Cl, OMe) underwent the reaction unless the phenyl substituent was too strongly electron withdrawing (CN). Cross-coupling occurred exclusively in the ortho position relative to the carbamate group. The regioselectivity at the phenol (ortho or pa
APA, Harvard, Vancouver, ISO, and other styles
9

Nagaraju, Karre, and Dawei Ma. "Oxidative coupling strategies for the synthesis of indole alkaloids." Chemical Society Reviews 47, no. 21 (2018): 8018–29. http://dx.doi.org/10.1039/c8cs00305j.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Takizawa, Shinobu, Junpei Kodera, Yasushi Yoshida, et al. "ChemInform Abstract: Enantioselective Oxidative-Coupling of Polycyclic Phenols." ChemInform 45, no. 31 (2014): no. http://dx.doi.org/10.1002/chin.201431033.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Oxidative coupling of phenols"

1

Hoffmann, Eric. "The oxidative coupling of phenols using stoichiometric metal oxidants." Thesis, Nelson Mandela Metropolitan University, 2005. http://hdl.handle.net/10948/180.

Full text
Abstract:
The oxidative coupling of 2,6-di-t-butylphenol under mild reaction conditions is well documented and the subject of many patents. However, the coupling of other monoand di- substituted phenols is not as well documented and thus there is scope for further investigation for providing a convenient, environmentally friendly and economically viable method for the oxidative coupling of these phenols. In this study, the oxidative coupling of a variety of alkylated phenolic substrates, 2-tbutylphenol, 2,6-di-t-butylphenol, 2,4 -di-t-butylphenol and ,4-dimethylphenol, using a range of different oxidizi
APA, Harvard, Vancouver, ISO, and other styles
2

Setälä, Harri. "Regio- and stereoselectivity of oxidative coupling reaction of phenols : spirodienones as construction units in ligin /." [Espoo, Finland] : VTT, 2008. http://www.vtt.fi/inf/pdf/publications/2008/P689.pdf.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Fürtges, Leon [Verfasser], and Michael [Akademischer Betreuer] Müller. "Oxidative phenol coupling in ascomycetes: regioselectivity of coupling enzymes." Freiburg : Universität, 2018. http://d-nb.info/1163945870/34.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Fukuoka, Tokuma. "Synthesis of novel functional polymeric materials via oxidative coupling of phenols by peroxidase and its model complex." 京都大学 (Kyoto University), 2005. http://hdl.handle.net/2433/144883.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Denizot, Natacha. "Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles." Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLS147/document.

Full text
Abstract:
Le noyau benzofuro[2,3-b]indoline est une structure complexe que l’on retrouve dans différentes substances naturelles telles que l’azonazine, la voacalgine A, la bipleiophylline ou encore le diazonamide A. Ces produits naturels possèdent une activité biologique intéressante et plus particulièrement le diazonamide A avec un IC50 inférieur à 15ng/mL sur plusieurs lignées cellulaires cancéreuses. De plus, certaines de ces substances n’ont jamais été synthétisées à ce jour. Lors de la biogénèse de ces composés, il est supposé que le motif benzofuroindoline est créé par un couplage oxydant entre un
APA, Harvard, Vancouver, ISO, and other styles
6

Beaud, Rodolphe. "Hydroarylation régiosélective d’indoles pour l’accès aux motifs 3 - arylindolines : études et applications d’une nouvelle réactivité de l’indole." Thesis, Paris 11, 2014. http://www.theses.fr/2014PA112308/document.

Full text
Abstract:
Le diazonamide A, molécule naturelle extraite d’une ascidie marine, présente une activité antitumorale très importante (IC₅₀ < 5 nM) selon un mode d’action tout à fait original. Des études ont en effet prouvé que cette molécule inhibait une enzyme, l’Ornithine-d-aminotransferase, intervenant dans la réplication cellulaire des cellules cancéreuses faisant d’elle un poison du fuseau mitotique très sélectif. Cette molécule présente en son sein un cœur benzofuroindoline qui serait issu, d’un point de vue biogénétique, d’un couplage oxydant entre un noyau indole et un noyau phénol. Afin de dével
APA, Harvard, Vancouver, ISO, and other styles
7

Lee, Kerri-Ann S. "Oxidative coupling of sinapic acid." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq23377.pdf.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Ji, Jianhua. "Regioselective Coupling Reactions of Diiodophenol Derivatives." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc277926/.

Full text
Abstract:
Palladium catalyzed reactions of derivatives of 2,4-diiodophenol are explored. Coupling reactions with a series of terminal alkynes and formylation are found to be efficient and regioselective. Coupling with stananne reagents and alkenes do not work. The nature of the oxygen protecting group is critical. The phytotoxic natural product, Eutypine, is synthesized by using regioselective formylation and alkyne coupling. An approach to the plant antimicrobial compound Plicatin B is examined.
APA, Harvard, Vancouver, ISO, and other styles
9

Hargreaves, J. S. J. "The catalysed oxidative coupling of methane." Thesis, University of Liverpool, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.303659.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

You, Shaochun. "CuCl₂-induced oxidative coupling of Anions /." Bern, 1992. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Oxidative coupling of phenols"

1

Koning, Cornelis Eme. Polymer-bound Dmap-copper complexes as catalysts for the oxidative coupling of phenols. Veenstra, 1987.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Lei, Aiwen, Wei Shi, Chao Liu, Wei Liu, Hua Zhang, and Chuan He. Oxidative Cross-Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527680986.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Lei, Aiwen, ed. Transition Metal Catalyzed Oxidative Cross-Coupling Reactions. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-58104-9.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Kimkes, Peter. Oxidative coupling polymerization of primary aromatic diamines. [s.n.], 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Johannes Maria Nicolaas van Kasteren. Oxidative coupling of methane over lithium promoted magnesia. [s.n.], 1990.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

M, De Pontes, ed. Natural gas conversion IV: Proceedings of the 4th International Natural Gas Conversion Symposium, Kruger Park, South Africa, November 19-23, 1995. Elsevier, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Liu, Wei, Wei Shi, Chao Liu, Hua Zhang, and Aiwen Lei. Oxidative Cross-Coupling Reactions. Wiley & Sons, Limited, John, 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Liu, Wei, Wei Shi, Chao Liu, Hua Zhang, and Aiwen Lei. Oxidative Cross-Coupling Reactions. Wiley & Sons, Limited, John, 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Liu, Wei, Wei Shi, Chao Liu, Hua Zhang, and Aiwen Lei. Oxidative Cross-Coupling Reactions. Wiley & Sons, Incorporated, John, 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Liu, Wei, Wei Shi, Chao Liu, Hua Zhang, and Aiwen Lei. Oxidative Cross-Coupling Reactions. Wiley & Sons, Incorporated, John, 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Oxidative coupling of phenols"

1

Brunow, Gösta, Ilkka Kilpeläinen, Jussi Sipilä, et al. "Oxidative Coupling of Phenols and the Biosynthesis of Lignin." In ACS Symposium Series. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0697.ch010.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Huang, Qingguo, and Walter J. Weber. "Peroxidase-Catalyzed Oxidative Coupling of Phenols in the Presence of Geosorbents." In ACS Symposium Series. American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0904.ch003.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Odagi, Minami, and Kazuo Nagasawa. "Oxidative Phenolic Coupling Reaction/Aza-Michael Reaction Strategy for the Synthesis of Complex Polycyclic Alkaloids." In Modern Natural Product Synthesis. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1619-7_10.

Full text
Abstract:
AbstractThe synthesis of alkaloids featuring fused polycyclic frameworks has long attracted the interest of synthetic organic communities, owing to their great structural complexity and wide variety of biological activities. Indeed, a variety of strategies for synthesizing these alkaloids have been investigated over the years. Here, we present our innovative strategy for tahe construction of complex fused polycyclic frameworks via oxidative phenolic coupling reaction and subsequent regioselective intramolecular aza-Michael reaction. We illustrate its practical application in synthetic studies
APA, Harvard, Vancouver, ISO, and other styles
4

Gooch, Jan W. "Oxidative Coupling." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8316.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Clifford, Tom, and Glyn Howatson. "(Poly)phenols in Exercise Performance and Recovery." In Oxidative Eustress in Exercise Physiology. CRC Press, 2022. http://dx.doi.org/10.1201/9781003051619-13.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Xie, Nan-Sheng, Quan-Zhong Liu, Zhi-Bin Luo, et al. "Oxidative CC Coupling." In Regio- and Stereo- Controlled Oxidations and Reductions. John Wiley & Sons, Ltd, 2007. http://dx.doi.org/10.1002/9780470090244.ch8.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Caro, Juergen. "Oxidative Coupling in Membrane Reactors." In Encyclopedia of Membranes. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_734-6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Caro, Juergen. "Oxidative Coupling in Membrane Reactors." In Encyclopedia of Membranes. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_734.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Robinson, Joseph D. "Oxidative Phosphorylation: Chemical-Coupling Hypothesis." In Moving Questions. Springer New York, 1997. http://dx.doi.org/10.1007/978-1-4614-7600-9_16.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Robinson, Joseph D. "Oxidative Phosphorylation: Chemiosmotic Coupling Hypothesis." In Moving Questions. Springer New York, 1997. http://dx.doi.org/10.1007/978-1-4614-7600-9_17.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Oxidative coupling of phenols"

1

Monte, S. J., and G. Sugerman. "High Temperature Inorganic Anti-Corrosive Coatings Using Organometallic Titanate and Zirconate Quat Blends (QB)." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90432.

Full text
Abstract:
Abstract Organosoluble and hydrolytically stable liquid pyrophosphato functional titanate and zirconate organometallic coupling agents are converted into water soluble salts via quaternization with certain methacrylic and acrylic functional amines. The resultant individual quats may be combined to form Quat Blends (QB's) having new and novel synergistic performance benefits in unfilled and particulate filled inks, coatings and films. Previous work by the authors is referenced to gain a historical perspective of evolved chemistry and performance efficacy. Data shows QB additive containing coati
APA, Harvard, Vancouver, ISO, and other styles
2

Renneberg, Bernd, and Werner Breitenstein. "Coupling of Phenols to 2-Chlorotrityl Resins under Non-basic Conditions." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01760.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

MARIN, G. B. "HIGH TEMPERATURE OXIDATION PROCESSES: OXIDATIVE COUPLING OF METHANE." In Proceedings of the NIOK (Netherlands Institute for Catalysis Research) Course on Catalytic Oxidation. WORLD SCIENTIFIC, 1995. http://dx.doi.org/10.1142/9789814503884_0006.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Limberger, Jones, and Adriano Lisboa Monteiro. "Copper Catalyzed C-O and C-N Coupling of Vinyl Bromides with Phenols and Azoles." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0149-1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Al-Safar, Marwa A., and Mohammed S. Al-Enizzi. "Spectrophotometric determination of salbutamol via oxidative coupling reaction using reagent benzidine." In 1ST SAMARRA INTERNATIONAL CONFERENCE FOR PURE AND APPLIED SCIENCES (SICPS2021): SICPS2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0121660.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Yao, Cheng, Changping Zhu, Qiang Wu, Minglei Shan, and Bingyan Chen. "Coupling mechanism between Ozone and dual frequency ultrasound in advanced oxidative process." In 2016 IEEE International Conference on Consumer Electronics-Taiwan (ICCE-TW). IEEE, 2016. http://dx.doi.org/10.1109/icce-tw.2016.7520942.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Al-Falluji, Mustafa Mohammed, Maadh T. Abdulrahman, and Ali Ibraheem Khaleel. "Spectrophotometric determination of cefixime trihydrate via oxidative coupling reaction with amino phenazone." In 1ST SAMARRA INTERNATIONAL CONFERENCE FOR PURE AND APPLIED SCIENCES (SICPS2021): SICPS2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0121113.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Dhivyaprabha, T. T., M. B. Jennyfer Susan, P. Lalitha, P. Subashini, D. Kamilini, and R. Vijayabhanu. "Predicting ethylene production in oxidative coupling of methane: A machine learning approach." In FOURTH INTERNATIONAL CONFERENCE ON ADVANCES IN PHYSICAL SCIENCES AND MATERIALS: ICAPSM 2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0216039.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Muteb, Noor T., and Saad H. Sultan. "Spectrophotometric determination of promethazine hydrochloride using oxidative coupling reactions with sulphacetamide sodium salt." In THE 5TH INTERNATIONAL CONFERENCE ON BUILDINGS, CONSTRUCTION, AND ENVIRONMENTAL ENGINEERING: BCEE5. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0238118.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Hussein, Ali M., and Nebbel S. Othman. "Development spectrophotometric determination of trifluoperazine hydrochloride in dosage forms by used oxidative coupling reaction." In 1ST INTERNATIONAL CONFERENCE ON ACHIEVING THE SUSTAINABLE DEVELOPMENT GOALS. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0136254.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Oxidative coupling of phenols"

1

Dr. Y.H. Ma, Dr. W.R. Moser, Dr. A.G. Dixon, Dr. A.M. Ramachandra, Dr. Y. Lu, and C. Binkerd. OXIDATIVE COUPLING OF METHANE USING INORGANIC MEMBRANE REACTORS. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/766717.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Pyrmak, Bill. Low-Energy, Low-Cost Ethylene Production by Low-Temperature Oxidative Coupling of Methane. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1843914.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Radaelli, Guido, Gaurav Chachra, and Divya Jonnavittula. Low-Energy, Low-Cost Production of Ethylene by Low- Temperature Oxidative Coupling of Methane. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1414280.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Tonkovich, A. L. Y., and R. W. Carr. A simulated countercurrent moving-bed chromatographic reactor for the oxidative coupling of methane: Experimental results. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10107209.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Taylor, R. The oxidative coupling of methane by lanthanum oxide catalysts: The influence of phase morphology on catalytic properties. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6971824.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Weber, Jr, Walter J., and Hildegarde Selig. The Efficacy of Oxidative Coupling for Promoting In-Situ Immobilization of Hydroxylated Aromatics in Contaminated Soil and Sediment Systems. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/825747.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Weber, Walter J., and Hildeagarde Selig. The Efficacy of Oxidative Coupling for Promoting In-Situ Immobilization of Hydroxylated Aromatics in Contaminated Soil and Sediment Systems. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/825749.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Weber Jr., W. J. The Efficacy of Oxidative Coupling for Promoting In-Situ Immobilization of Hydroxylated Aromatics in Contaminated Soil and Sediments Systems - Final Report. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/775520.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7152421.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Weber, W. J., and A. Bhandari. The efficacy of oxidative coupling for promoting in-situ immobilization of hydroxylated aromatics in contaminated soil and sediment systems. 1998 annual progress report. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/13519.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Oxidative coupling of phenols' for particular source types:
Journal articles Dissertations / Theses Books
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!

To the bibliography