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Relevant bibliographies by topics / Phenylcyclohexan

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Academic literature on the topic 'Phenylcyclohexan'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Phenylcyclohexan"

1

Ali, A. Khalaf, M. Awad Ibrahim, I. El-Emary Talaat, and A. K. Abd El-Aal Hassan. "Modern Friedel-Crafts chemistry. Part-271. Alkylation of benzene with 1-benzyl- and 1-phenylcyclohexanols in the presence of H2SO4 and AICI3/CH3NO2 catalysts." Journal of Indian Chemical Society Vol. 83, Oct 2006 (2006): 1018–22. https://doi.org/10.5281/zenodo.5831323.

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Department of Chemistry, Faculty of Science, Assiut University, Assiut, Egypt E-mail : prof_khalaf@hotmail.com <em>Manuscript received 7 November 2005, revised 4 May 2006, accepted 3 July 2006</em> The alkylation of benzyene with 1-benzylcyclohexanol (3) gave a mixture of 2,3-benzobicyclo[3.3.1]nona-2- ene (8, 79%) and cyclohexyldiphenylmethane (10, 21%) with AICI<sub>3</sub>/CH<sub>3</sub>NO<sub>2</sub> catalyst and a mixture of 1-benzyl cyclohexene 5 (47.5%), 8 (8%), 10 (21.5%), 1-cyclopentyl-1,2-diphenylethane (12, 18%) and l-benzyl-1- \phenylcyclohexene (13, 4%)with H<sub>2</sub>SO<sub>4</

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2

Minyaev, Mikhail E., Dmitrii M. Roitershtein, Ilya E. Nifant'ev, Ivan V. Ananyev, Tatyana V. Minyaeva, and Timofey A. Mikhaylyev. "A structural study of (1RS,2SR,3RS,4SR,5RS)-2,4-dibenzoyl-1,3,5-triphenylcyclohexan-1-ol chloroform hemisolvate and (1RS,2SR,3RS,4SR,5RS)-2,4-dibenzoyl-1-phenyl-3,5-bis(2-methoxyphenyl)cyclohexan-1-ol." Acta Crystallographica Section C Structural Chemistry 71, no. 6 (2015): 491–98. http://dx.doi.org/10.1107/s2053229615009857.

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(1RS,2SR,3RS,4SR,5RS)-2,4-Dibenzoyl-1,3,5-triphenylcyclohexan-1-ol or (4-hydroxy-2,4,6-triphenylcyclohexane-1,3-diyl)bis(phenylmethanone), C38H32O3, (1), is formed as a by-product in the NaOH-catalyzed synthesis of 1,3,5-triphenylpentane-1,5-dione from acetophenone and benzaldehyde. Single crystals of the chloroform hemisolvate, C38H32O3·0.5CHCl3, were grown from chloroform. The structure has triclinic (P-1) symmetry. One diastereomer [as a pair of (1RS,2SR,3RS,4SR,5RS)-enantiomers] of (1) has been found in the crystal structure and confirmed by NMR studies. The dichoromethane hemisolvate has

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Maixner, J., B. Jurásek, M. Kohout, M. Kuchař, and P. Kačer. "X-ray powder diffraction data for (S)-Deschloroketamine hydrochloride, C13H18ClNO." Powder Diffraction 32, no. 3 (2017): 193–95. http://dx.doi.org/10.1017/s0885715617000586.

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X-ray powder diffraction data, unit-cell parameters, and space group for S-2-(methylamino)-2-phenylcyclohexan-1-one hydrochloride, C13H18ClNO, are reported [a = 6.578 (1) Å, b = 13.250 (2) Å, c = 15.096 (2) Å, β = 91.619 (3)°, unit-cell volume V = 1315(1) Å3, Z = 4, and space group P21]. All measured lines were indexed and are consistent with the P21 space group. No detectable impurities were observed.

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Periasamy, M., L. Anjana, S. Athimoolam, A. Ponnuswamy, and S. Natarajan. "3-Bromo-2-ethoxy-2-phenylcyclohexan-1-one oxime." Acta Crystallographica Section E Structure Reports Online 62, no. 11 (2006): o5116—o5118. http://dx.doi.org/10.1107/s1600536806042371.

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A., A. FADDA, and EL-HOUSSINI M.S. "Synthesis of Cyclic Ketones by Activated Nitriles." Journal of Indian Chemical Society Vol. 67, Nov 1990 (1990): 915–17. https://doi.org/10.5281/zenodo.6257458.

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Department of Chemistry, Faculty of Science, Mansoura University, Mansoura,Egypt <em>Manuscript received 10 April 1990, revised 10 September 1990, accepted 13 October 1990</em> Synthesis of Cyclic Ketones by Activated Nitriles

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Senanayake, Chris H., Robert D. Larsen, Lisa M. DiMichele, et al. "Asymmetric synthesis of conformationally constrained cis-1-amino-1-phenylcyclohexan-2-ol." Tetrahedron: Asymmetry 7, no. 5 (1996): 1501–6. http://dx.doi.org/10.1016/0957-4166(96)00169-3.

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SENANAYAKE, C. H., R. D. LARSEN, L. M. DIMICHELE, et al. "ChemInform Abstract: Asymmetric Synthesis of Conformationally Constrained cis-1-Amino-1- phenylcyclohexan-2-ol." ChemInform 27, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199640030.

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Basavaiah, D., та T. K. Bharathi. "Enantioselective synthesis of α- and β-hydroxy acids using -2-phenylcyclohexan-1-ol-as chiral auxiliary". Tetrahedron Letters 32, № 28 (1991): 3417–20. http://dx.doi.org/10.1016/s0040-4039(00)92724-2.

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Pincock, J. A., S. Rifai, and R. Stefanova. "The photochemistry of the 4-cyanobenzoic acid esters of trans- and cis-2-phenylcyclohexanol." Canadian Journal of Chemistry 79, no. 1 (2001): 63–69. http://dx.doi.org/10.1139/v00-167.

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Irradiation of trans-2-phenylcyclohexyl 4-cyanobenzoate (4) in methanol results in formation of the 1-phenylcyclohexene and 4-cyanobenzoic acid as the major products. The mechanism proposed for this example of the Norrish Type II-like reaction, normally inefficient for the π,π* state of esters, begins with intramolecular electron transfer in the excited singlet state. The next step, intramolecular proton transfer, is highly exergonic as a result of the increased acidity of the benzylic hydrogen of the radical cation and the increased basicity of the carbonyl oxygen of the radical anion. The fi

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BASAVAIAH, D., та T. K. BHARATHI. "ChemInform Abstract: Enantioselective Synthesis of α- and β-Hydroxy Acids Using trans-2-Phenylcyclohexan-1-ol as Chiral Auxiliary." ChemInform 23, № 16 (2010): no. http://dx.doi.org/10.1002/chin.199216072.

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Dissertations / Theses on the topic "Phenylcyclohexan"

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Tyson, D. G. "Optical and static Kerr effects in phenylcyclohexane homologues." Thesis, University of Reading, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234367.

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Parola, Lisa 1964. "Ovarian toxicity of 4-phenylcyclohexene in female B6C3F1 mice." Thesis, The University of Arizona, 1991. http://hdl.handle.net/10150/291330.

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4-Phenylcyclohexene (4PC), a contaminant released from latex adhesives used to produce carpet, is structurally similar to the ovarian toxicant, 4-vinylcyclohexene (VCH). VCH causes depletion of primary ovarian follicles in mice. Our aim was to determine if the related compound, 4PC, also causes ovarian damage. Groups of B6C3F1 mice were given either: sesame seed oil (vehicle control), 3 mmole/kg 4PC (4PC-3), 6 mmole/kg 4PC (4PC-6), or 6 mmole/kg VCH (positive control), ip, daily for 30 days. Vaginal smears were done daily to determine the stage of estrus. On day 31, the mice were killed and th

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Demer, Frank Robert 1961. "The impact of various cure parameters on the release of 4-phenylcyclohexene from carboxylated styrene-butadiene rubber latex." Thesis, The University of Arizona, 1989. http://hdl.handle.net/10150/277075.

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Research was initiated to examine the feasibility of removing the majority of 4-PCH from the XSBR latex employed in carpet manufacturing. The reduction of 4-PCH from such latices would lend insight into the control of certain carpet related illnesses.

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Walsh, Dale Warner 1961. "PRELIMINARY EVALUATION OF THE ENVIRONMENTAL CONCENTRATION AND TOXICITY OF 4-PHENYLCYCLOHEXENE: AN EMISSION OF NEW CARPETING (ODOR, HEALTH, INDOOR)." Thesis, The University of Arizona, 1986. http://hdl.handle.net/10150/276881.

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Flos, Manon. "Synthèse et analyse conformationnelle de dérivés du cannabidiol : vers l’atropisomérie autour de la liaison aryl-C(sp3)." Thesis, Reims, 2017. http://www.theses.fr/2017REIMP201/document.

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Le cannabidiol (CBD), constituant majeur non-psychotrope du Cannabis sativa, possède un grand nombre de propriétés pharmacologiques. Des dérivés du CBD présentant une rotation restreinte autour de la liaison simple aryl-C(sp3) ont été synthétisés avec deux modifications majeures apportés sur l’un ou/et l’autre cycle dans le but d’atteindre et de contrôler l’atropisomérie.Des phénylcyclohexanes diversement substitués ont été préparés par hydrogénation catalytique des phénylcyclohexènes correspondants. Des études de RMN dynamique et de modélisation moléculaire ont permis l’identification des épi

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Leforce, Mary Hall 1949. "Investigation of the effects of various cure parameters on the release of 4-phenylcyclohexene from carpet backed with styrene-butadiene rubber latex." Thesis, The University of Arizona, 1991. http://hdl.handle.net/10150/277857.

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The effects of cure time, cure temperature, and air circulation on the release of 4-phenylcyclohexene (4-PCH) in tufted carpet backed with carboxylated styrene-butadiene rubber (SBR) latex were examined in this research project. 4-PCH is a suspect cause of certain "building-related" illnesses such as headache, upper respiratory and eye irritation, and fatigue. A standardized method for preparing carpet backed with SBR latex and analyzing its 4-PCH content was developed. The cure parameters investigated included three cure temperatures (225, 250 and 275°F), six cure times (0, 5, 10, 20, 40 and

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Zhang, Jin 1961. "The impact of air velocity and other various cure parameters on the release of 4-phenylcyclohexene (4-PCH) from carpet backed with carboxylated SBR latex." Thesis, The University of Arizona, 1990. http://hdl.handle.net/10150/277330.

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This research evaluated the effect of air velocity and other cure parameters, such as temperature and oven air recirculation, on the release of 4-Phenylcyclohexene from carpet samples coated with a composite XSBR latex. This kind of carpet is similar to that used in industries. The effect of latex frothing process on the reduction of 4-PCH from SBR latex samples was also investigated. It has been found that both air velocity and oven temperature were important cure parameters in 4-PCH reduction. Air velocity was the dominating factor in the removal of 4-PCH from carpet back-coated with latex c

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Book chapters on the topic "Phenylcyclohexan"

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Hirzy, J. William, and Rufus Morison. "Carpet/4-Phenylcyclohexene Toxicity: The EPA Headquarters Case." In The Analysis, Communication, and Perception of Risk. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-2370-7_6.

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2

Winkelmann, Jochen. "Diffusion coefficient of 1-(1-phenylcyclohexyl)-piperidine in water." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_894.

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3

"1-Phenylcyclohexyl-Piperidin." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_312941.

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4

Eames, J. "Resolution of -2-Phenylcyclohexanol." In Alcohols. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00276.

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Eames, J. "Resolution of 2-Phenylcyclohex-2-en-1-ol." In Alcohols. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00334.

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Winter, Jerrold. "Dissociative Anesthetics: Angel Dust to Special K to Ketamine Clinics." In Our Love Affair with Drugs. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780190051464.003.0010.

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We will consider just two drugs in this chapter. They are phencyclidine and ketamine. Both are widely used as anesthetic agents, ketamine in humans and phencyclidine in animals. The acronym for phencyclidine that we will use, PCP, comes from its chemical name 1-(1-PhenylCyclohexyl)-Piperidine. In addition to their medical use, both ketamine and PCP have gained roles as recreational drugs or, as others would put it, drugs of abuse. While sharing some of the properties of the depressant drugs we met in the preceding chapter, PCP and ketamine are pharmacologically and therapeutically unique. On

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Conference papers on the topic "Phenylcyclohexan"

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Szczucinski, T., Roman S. Dabrowski, Janusz Parka, and Jerzy Kedzierski. "Phenylcyclohexanes containing ketogroup." In Liquid Crystals, edited by Marzena Tykarska, Roman S. Dabrowski, and Jerzy Zielinski. SPIE, 1998. http://dx.doi.org/10.1117/12.301321.

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Frech, Cheryl B., B. M. Fung, and Martin Schadt. "Orientational Ordering Of Phenylcyclohexane-Based Liquid Crystals Determined From Carbon-13 2D NMR Spectroscopy." In OE/LASE '89, edited by J. William Doane and Zvi Yaniv. SPIE, 1989. http://dx.doi.org/10.1117/12.976422.

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