Relevant bibliographies by topics / Cyclohexanol derivative

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  2. Dissertations / Theses
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Academic literature on the topic 'Cyclohexanol derivative'

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

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Journal articles on the topic "Cyclohexanol derivative"

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Sun, Cheng Guo, Bing Cheng Hu, and Quan Zhi Deng. "The Effect of Disulphide Bond in Metallodeuteroporphyrin on Their Catalytic Activity for Aerobic Oxidation of Cyclohexane." Advanced Materials Research 233-235 (May 2011): 427–30. http://dx.doi.org/10.4028/www.scientific.net/amr.233-235.427.

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Two novel types of metallo-deuteroporphyrins bearing the disulphide bond were employed to investigate their catalytic activity in oxidation of cyclohexane with molecular oxygen (air) to cyclohexanol and cyclohexanone without the use of sacrificial co-reductant. The catalytic activity of metallo-deuteroporphyrin disulphide derivatives was obvious difference when different metals were incorporated into the porphyrin. However, the same metal cobalt porphyrin complexes exhibited the different catalytic efficiency due to the effect of substituents. Co(II)deuteroporphyrin disulphide derivative is mor
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Rocco, Dalila, Catherine E. Housecroft, and Edwin C. Constable. "Synthesis of Terpyridines: Simple Reactions—What Could Possibly Go Wrong?" Molecules 24, no. 9 (2019): 1799. http://dx.doi.org/10.3390/molecules24091799.

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The preparation of 24-functionalized 12,22:26,32-terpyridines (4′-functionalized 3,2:6′,3″-terpyridines) by the reaction of three 4-alkoxybenzaldehydes with 3-acetylpyridine and ammonia was investigated; under identical reaction conditions, two (R =nC4H9, C2H5) gave the expected products whereas a third (R = nC3H7) gave only a cyclohexanol derivative derived from the condensation of three molecules of 3-acetylpyridine with two of 4-(n-propoxy)benzaldehyde. A comprehensive survey of “unexpected” products from reactions of ArCOCH3 derivatives with aromatic aldehydes is presented. Three different
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Kirillova, Marina V., Polyana Tomé de Paiva, Wagner A. Carvalho, Dalmo Mandelli, and Alexander M. Kirillov. "Mixed-ligand aminoalcohol-dicarboxylate copper(II) coordination polymers as catalysts for the oxidative functionalization of cyclic alkanes and alkenes." Pure and Applied Chemistry 89, no. 1 (2017): 61–73. http://dx.doi.org/10.1515/pac-2016-1012.

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AbstractNew copper(II) catalytic systems for the mild oxidative C–H functionalization of cycloalkanes and cycloalkenes were developed, which are based on a series of mixed-ligand aminoalcohol-dicarboxylate coordination polymers, namely [Cu2(μ-dmea)2(μ-nda)(H2O)2]n·2nH2O (1), [Cu2(μ-Hmdea)2(μ-nda)]n·2nH2O (2), and [Cu2(μ-Hbdea)2(μ-nda)]n·2nH2O (3) that bear slightly different dicopper(II) aminoalcoholate cores, as well as on a structurally distinct dicopper(II) [Cu2(H4etda)2(μ-nda)]·nda·4H2O (4) derivative [abbreviations: H2nda, 2,6-naphthalenedicarboxylic acid; Hdmea, N,N′-dimethylethanolamine
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Alikulov, R.V.* Alimnazarov B.Kh. Geldiev Yu.A. Suyunov Zh.R. &. Shukurov D.Kh. "STRUCTURES LUTERGININA." INTERNATIONAL JOURNAL OF ENGINEERING SCIENCES & RESEARCH TECHNOLOGY 8, no. 6 (2019): 273–76. https://doi.org/10.5281/zenodo.3256175.

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In this work, we studied the IR, UV, PMR and mass spectra, chemical transformations of lutherginin and its derivatives of homoproporphine alkaloids of time-lapse. According to the given spectral data, this compound is assigned to the homoproporphine base group with a spiro cyclohexanol ring. When establishing the structure of luterginine, its various spectral data and numerous chemical transformations were studied. The most important of them can be considered following with the action of acetic anhydride and acetic acid sodium from the base obtained O, N-diacetyl derivative, indicating the pre
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Kitahara, Takeshi, and Kenji Mor. "Preparation of chiral cyclohexanol derivative with high optical purity by yeast reduction." Tetrahedron Letters 26, no. 4 (1985): 451–52. http://dx.doi.org/10.1016/s0040-4039(00)61908-1.

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Muth, Eric A., John T. Haskins, John A. Moyer, George E. M. Husbands, Susan T. Nielsen, and Ernest B. Sigg. "Antidepressant biochemical profile of the novel bicyclic compound Wy-45,030, an ethyl cyclohexanol derivative." Biochemical Pharmacology 35, no. 24 (1986): 4493–97. http://dx.doi.org/10.1016/0006-2952(86)90769-0.

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Deforth, T., M. Kaschke, H. Stock, H. Pritzkow, and W. Siebert. "Synthesis of C2B3 X-Heterocycles (X = C, N, P, O, S) from 1,3,5-Triborapentanes." Zeitschrift für Naturforschung B 52, no. 7 (1997): 823–30. http://dx.doi.org/10.1515/znb-1997-0711.

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Abstract The hydroboration of acetylene with HBCl2 yields the products (Cl2B)2CHMe (1a), (Cl2BCHMe)2BCl (2a), (Cl2BCHMeBCl)2CHMe (3a), and (ClBCHMe)3 (4a). The crystal structure of 4a as well as of the pentaiodo derivative 2b were determined. A mechanism for the formation of the different hydroboration products is proposed. The 1,3,5-triborapentane 2a serves as precursor for the synthesis of derivatives of 1,3,5-triboracyclohexanes, 1,3,5-tribora-2-aza-cyclohexanes, 1,3,5-tribora-2-phospha-cyclo-hexanes, and 1,3,5-tribora-2-thia-cyclohexanes. Their constitutions have been derived from spectros
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Chen, Changzhou, Peng Liu, Minghao Zhou, Brajendra K. Sharma, and Jianchun Jiang. "Selective Hydrogenation of Phenol to Cyclohexanol over Ni/CNT in the Absence of External Hydrogen." Energies 13, no. 4 (2020): 846. http://dx.doi.org/10.3390/en13040846.

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Transfer hydrogenation is a novel and efficient method to realize the hydrogenation in different chemical reactions and exploring a simple heterogeneous catalyst with high activity is crucial. Ni/CNT was synthesized through a traditional impregnation method, and the detailed physicochemical properties were performed by means of XRD, TEM, XPS, BET, and ICP analysis. Through the screening of loading amounts, solvents, reaction temperature, and reaction time, 20% Ni/CNT achieves an almost complete conversion of phenol after 60 min at 220 °C in the absence of external hydrogen. Furthermore, the ca
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Mohareb, Rafat Milad, Rehab Ali Ibrahim, Amira Mohamed Elmetwally, and Marwa Soliman Gamaan. "Synthesis of Fused Quinoline Derivatives with Antiproliferative Activities and Tyrosine Kinases, Pim-1 Kinase Inhibitions." Acta Chimica Slovenica 69, no. 1 (2022): 13–29. https://doi.org/10.17344/acsi.2021.6733.

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Cyclohexan-1,3-dione (1) reacted with either 2-aminoprop-1-ene-1,1,3-tricarbonitrile (2a) or diethyl 3-amino-2-cyanopent-2-enedioate (2b) to give the 5,6,7,8-tetrahydronaphthalene derivatives 3a and 3b, respectively. The latter compounds underwent further heterocyclization reactions to give the thieno[2’,3’:5,6]benzo[1,2-e][1,3]oxazine derivatives. On the other hand, the reaction of compound 1 with trichloroacetonitrile afforded the (2,2,2-trichloroethylidene)cyclohexane derivative 14. The latter underwent a series of reactions to produce 2,3,6,7-tetrahydroquinazoline, dihydrothieno[2,3-h]isoq
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Bhattacharjee, Rita, and Virupaiah Gayathri. "Synthesis and Characterization of Ru(III) Complexes Containing Quinazoline Derivatives and their Biological and Catalytic Activities." Asian Journal of Chemistry 35, no. 7 (2023): 1645–50. http://dx.doi.org/10.14233/ajchem.2023.27941.

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Ruthenium trichloride trihydrate (RuCl3·3H2O) reacted with quinazoline derivative ligands (L) in 1:1 mole ratio in acetone to yield a series of brown/green/greenish black ruthenium(III) complexes of the type RuX3L·nH2O where X = Cl, n = 0, 1, 2 and 3 and L is 6-R-5,6-dihydrobenzoimidazo[1,2- c]quinazoline (R = ethyl: L1/n or i-propyl: L2, L3/n or i-butyl: L4, L5/phenyl: L6/furyl: L7/thiophenyl: L8/o or p-hydroxyphenyl: L9, L10/o or p-chlorophenyl: L11, L12/dimethylaminophenyl: L13). All the synthesized Ru(III) complexes were characterized by elemental analyses, conductivity measurements, infra
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Dissertations / Theses on the topic "Cyclohexanol derivative"

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Yazicioglu, Emre Yusuf. "Transformation Of Cyclohexanone Derivatives To Bicyclic Furan And Pyrrole Derivatives." Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605269/index.pdf.

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Tetrahydrobenzofurans and tetrahydroindoles are two very valuable classes of substances which have wide usage area<br>either as starting materials for drug substances or many other compounds which have fused heterocyclic rings in their structures and pharmacophore for many complex natural products<br>syntheses of derivatives of these compounds with different substitution patterns, is an exciting challenge for many scientists. Benzofuran and tetrahydroindole derivatives, which are potent bioactive substances, are synthesized from various cyclohexanone derivatives that are allylated by Stork-ena
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Miciak, A. "The effects of some cyclohexanol derivatives on rat hepatic sterol synthesis." Thesis, University of Nottingham, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355294.

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Sutton, Peter William. "Ketene cycloadditions to cyclohexa-3,5-diene-cis-1,2-diol acetals : preparation of polyhydroxylated cyclohexane derivatives." Thesis, University of Exeter, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294477.

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Driega, Alex B. (Alexander Brooke) Carleton University Dissertation Chemistry. "An analysis of factors contributing to isotropic [superscript] 13C shifts in 1,2- Dialkoxybenzene and Cyclohexane derivatives." Ottawa, 1992.

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Crews, Everett III. "Retroaldo-trapping reactions of [beta]-hydroxy-[alpha]-phenylsulfenyl cyclohexanone and decalone derivatives and the total synthesis of the California red scale sex pheromone." Diss., Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/27404.

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Renouf, Philippe. "Synthèse asymétrique par hydrolyse enzymatique de diacétates de diénols prochiraux. Nouvelle voie d'accès à des composés optiquement purs." Rouen, 1995. http://www.theses.fr/1995ROUES048.

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Une nouvelle synthèse énantiosélective de composés chiraux originaux, possédant un centre stéréogénique quaternaire, a été mise au point, par hydrolyse enzymatique de diacétates de diénols prochiraux. En traitant les 2,4-diacétoxy-cyclohexa-1,4-diènes 3,3-disubstitués par le candida cylindracea lipase, nous obtenons les cétoacétates d'énols correspondants optiquement purs (ee>98%) avec des rendements chimiques élevés. Les excès énantiomériques ont été déterminés par RMN1H en présence de chélates de terre rare à ligands chiraux et/ou par CPG sur phase chirale. La configuration absolue de deux d
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Meyer, Luc. "Auxiliaires chiraux à centre d'aiguillage : nouveaux outils en synthèse asymétrique. Application à la synthèse d'α-aminoacides de configuration (R) ou (S)". Rouen, 1997. http://www.theses.fr/1997ROUES063.

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De nouveaux outils pour la synthèse asymétrique sont proposés : des auxiliaires chiraux à centre d'aiguillage (R,S). Le passage du (1R,2S,5R)-2-diméthylphénylméthyl-5-méthylcyclohexyl carbaldéhyde à l'imine correspondante du glycinate de méthyle, suivi de la déprotonation (diisopropylamidure de lithium), puis de l'alkylation par des halogénures d'alkyles conduit après hydrolyse à des α-aminoacides de configuration (R) avec des e. E. >98%. Il a été montré que pour obtenir les α-aminoacides de configuration (S), il n'était pas nécessaire d'inverser la totalité des centres stéréogéniques de l'ald
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chi-han, Chen, and 陳錡翰. "Enantioselective synthesis of multi-substituted cyclohexanone derivatives via organocatalytic asymmetric double michael addition." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/20853687948437223723.

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碩士<br>國立臺灣師範大學<br>化學系<br>102<br>organocatalytic asymmetric double Michael addition reaction of a,b-unsaturated-1,3-diketones to 2-alkylidene malononitriles 80 has been investigated with quinine as the catalyst to afford a range of multi-substituted cyclohexanones bearing two sterecenters in good results (58-94% yield, >99:1 de, and up to 92% ee).
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Ko, Chi-Ting, and 柯紀廷. "Enantioselective synthesis of spiro cyclohexanone derivatives using cinchona alkaloid derived primary amine as organocatalyst." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/g98f9r.

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Hossain, Subharaj. "Shock tube experimental and advanced computational investigations on pyrolysis of cyclohexane derivatives and C2 + C2 reaction." Thesis, 2022. https://etd.iisc.ac.in/handle/2005/5795.

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My thesis involves studying the pyrolysis/thermal decomposition of cyclohexane derivatives (important constituents of conventional transportation fuel). From the literature as well as the composition analysis of two fuels (JP-7(eq) and RP-1) performed in our lab using GC-MS, we found that cyclohexane derivatives can be categorized into different types: single side-chain alkylcyclohexane; multiple side-chain alkylcyclohexane, and decalin (two fused cyclohexane ring). We have taken iso-propylcyclohexane as a member of single side-chain alkylcyclohexane and 1,3,5-trimethylcyclohexane as a m
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Books on the topic "Cyclohexanol derivative"

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Nesterov, S. V. Dicyclohexanocrown ethers: From synthesis to radiochemical applications. Nova Science Publishers, 2011.

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Wang, Zhandong. Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2.

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Wang, Zhandong. Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer, 2018.

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Wang, Zhandong. Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer, 2019.

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Book chapters on the topic "Cyclohexanol derivative"

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Huo, Zhibao. "Highly Selective Hydrothermal Production of Cyclohexanol from Biomass-Derived Cyclohexanone Over Cu Powder." In Diverse Hydrogen Sources for Biomass-derivatives Conversion. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-1673-3_8.

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Wang, Zhandong. "Combustion Kinetics of Cyclohexane and C1–C2 Mono-alkyl Cyclohexanes." In Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2_6.

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Wang, Zhandong. "Experimental and Modeling Study of Cyclohexane Combustion." In Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2_3.

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Wang, Zhandong. "Introduction." In Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2_1.

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Wang, Zhandong. "Experimental Method and Kinetic Modeling." In Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2_2.

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Wang, Zhandong. "Experimental and Modeling Study of Methylcyclohexane Combustion." In Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2_4.

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Wang, Zhandong. "Experimental and Modeling Study of Ethylcyclohexane Combustion." In Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2_5.

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Wang, Zhandong. "Conclusions and Perspective." In Experimental and Kinetic Modeling Study of Cyclohexane and Its Mono-alkylated Derivatives Combustion. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-5693-2_7.

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Varvaresou, Athanasia, Anna Tsantili-Kakoulidou, and Theodora Siatra-Papastaikoudi. "A Critical Appraisal of logP Calculation Procedures Using Experimental Octanol-Water and Cyclohexane-Water Partition Coefficients and HPLC Capacity Factors for a Series of Indole Containing Derivatives of 1,3,4-Thiadiazole and 1,2,4-Triazole." In Molecular Modeling and Prediction of Bioactivity. Springer US, 2000. http://dx.doi.org/10.1007/978-1-4615-4141-7_133.

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"Cyclohexane Derivatives." In Dictionary of Toxicology. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-9283-6_633.

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Conference papers on the topic "Cyclohexanol derivative"

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Peterson, Burl H., Sergey S. Sarkisov, V. N. Nesterov, et al. "New derivatives of cyclohexanone and piperidone compounds for bioluminous sensing." In Biomedical Optics 2006, edited by Samuel Achilefu, Darryl J. Bornhop, and Ramesh Raghavachari. SPIE, 2006. http://dx.doi.org/10.1117/12.641751.

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Bezborodov, Vladimir, Roman S. Dabrowski, Genadz Sasnouski, V. Lapanik, and Jerzy Dziaduszek. "New LC cyclohexene and cyclohexane derivatives: LC compositions on their base." In XIV Conference on Liquid Crystals, Chemistry, Physics, and Applications, edited by Jolanta Rutkowska, Stanislaw J. Klosowicz, and Jerzy Zielinski. SPIE, 2002. http://dx.doi.org/10.1117/12.472203.

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Yahaya, Muhammad, Muhamad Mat Salleh, and Akrajas Ali Umar. "Self-assembly layer of amino fluorenone derivative as optical receptor to detect cyclohexane vapour." In Microtechnologies for the New Millennium 2005, edited by Carles Cane, Jung-Chih Chiao, and Fernando Vidal Verdu. SPIE, 2005. http://dx.doi.org/10.1117/12.608493.

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