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Journal articles on the topic 'Phenylcyclohexan'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Abiero, Arvie, Raly James Perez Custodio, Chrislean Jun Botanas, et al. "1-Phenylcyclohexan-1-amine hydrochloride (PCA HCl) alters mesolimbic dopamine system accompanied by neuroplastic changes: A neuropsychopharmacological evaluation in rodents." Neurochemistry International 144 (March 2021): 104962. http://dx.doi.org/10.1016/j.neuint.2021.104962.

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12

Tobe, Yoshito, Hidekazu Iketani, Yuko Tsuchiya, Masayoshi Konishi, and Koichiro Naemura. "Homochiral ligands derived from cis-1-phenylcyclohexane-1,2-diol and cis-2-azido-2-phenylcyclohexanol." Tetrahedron: Asymmetry 8, no. 22 (1997): 3735–44. http://dx.doi.org/10.1016/s0957-4166(97)00552-1.

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13

TOBE, Y., H. IKETANI, Y. TSUCHIYA, M. KONISHI, and K. NAEMURA. "ChemInform Abstract: Homochiral Ligands Derived from cis-1-Phenylcyclohexane-1,2-diol and cis-2-Azido-2-phenylcyclohexanol." ChemInform 29, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199812034.

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14

Schaefer, Ted, Christian Beaulieu, and Rudy Sebastian. "2-Phenyladamantane as a model for axial phenylcyclohexane. 1H NMR and molecular orbital studies of motion about the Csp2—Csp3 bond." Canadian Journal of Chemistry 69, no. 3 (1991): 503–8. http://dx.doi.org/10.1139/v91-075.

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The 1H NMR spectra of the aromatic groups of 2-phenylcyclohexane and 2-phenyladamantane, in CS2/C6D12 solution at 300 K, are analyzed to yield the long-range coupling constants between the α and ring protons. The coupling over six bonds is related to the internal rotational potential about the Csp2—Csp3 bond in these molecules. It is confirmed that the equatorial isomer of phenylcyclohexane has the parallel conformer, that in which the aromatic plane lies in the symmetry plane bisecting the cyclohexane moiety, as the most stable. The apparent twofold barrier to rotation about the exocyclic car

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15

Hall, Emma A., and Stephen G. Bell. "The efficient and selective biocatalytic oxidation of norisoprenoid and aromatic substrates by CYP101B1 from Novosphingobium aromaticivorans DSM12444." RSC Advances 5, no. 8 (2015): 5762–73. http://dx.doi.org/10.1039/c4ra14010a.

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16

Wiberg, Kenneth B., Henry Castejon, William F. Bailey, and Joseph Ochterski. "Conformational Studies in the Cyclohexane Series. 2. Phenylcyclohexane and 1-Methyl-1-phenylcyclohexane." Journal of Organic Chemistry 65, no. 4 (2000): 1181–87. http://dx.doi.org/10.1021/jo9917386.

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17

Tomioka, Nozomi, Shinkoh Nanbu, Tomoyo Misawa-Suzuki, and Hirotaka Nagao. "N–C bond formation between two anilines coordinated to a ruthenium center in cis-form affording a 3,5-cyclohexadiene-1,2-diimine moiety." RSC Advances 11, no. 58 (2021): 36644–50. http://dx.doi.org/10.1039/d1ra07736h.

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Four-electron oxidation of two anilines coordinated to a ruthenium(ii) center in a cis-form affords N1-phenylcyclohexa-3,5-diene-1,2-diimine through an N–C bond formation with N–H and C–H bond activation.

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18

Parvez, Masood, Ian R. Hunt, and Brian A. Keay. "2-Phenylcyclohexyl 3-furancarboxylate." Acta Crystallographica Section E Structure Reports Online 57, no. 8 (2001): o802—o803. http://dx.doi.org/10.1107/s160053680101251x.

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19

Periasamy, M., Sudha Soundirapandian, S. Athimoolam, A. Ponnusamy, and S. Natarajan. "1-Naphthyl-4-phenylcyclohexene." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5651—o5653. http://dx.doi.org/10.1107/s1600536806047696.

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20

Wiberg, Kenneth B., Henry Castejon, William F. Bailey, and Joseph Ochterski. "ChemInform Abstract: Conformational Studies in the Cyclohexane Series. Part 2. Phenylcyclohexane and 1-Methyl-1-phenylcyclohexane." ChemInform 31, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.200022033.

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21

Goto, Hiromasa. "Preparation of Lyotropic Liquid Crystals and Optical Characterisation." International Letters of Chemistry, Physics and Astronomy 64 (February 2016): 171–77. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.64.171.

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Synthesis of an ionic liquid crystal (1-(6-(4-(4-trans-pentyl-cyclohexyl)-phenoxy)-hexyl)pyridinium chloride) showing lyotropic smectic phase was carried out. A simple reaction between phenylcyclohexane-type liquid crystal having halogen atom in the terminal and pyridine allows production of the ionic liquid crystal. The NMR measurements confirm chemical structure of the compound. Observation with polarsing optical microscopy evaluated that the compound shows fine multi-domains having fluidity. The lyotropic LC thus prepared displays smectic phase with layer structure.

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22

Goto, Hiromasa. "Preparation of Lyotropic Liquid Crystals and Optical Characterisation." International Letters of Chemistry, Physics and Astronomy 64 (February 15, 2016): 171–77. http://dx.doi.org/10.56431/p-m202au.

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Synthesis of an ionic liquid crystal (1-(6-(4-(4-trans-pentyl-cyclohexyl)-phenoxy)-hexyl)pyridinium chloride) showing lyotropic smectic phase was carried out. A simple reaction between phenylcyclohexane-type liquid crystal having halogen atom in the terminal and pyridine allows production of the ionic liquid crystal. The NMR measurements confirm chemical structure of the compound. Observation with polarsing optical microscopy evaluated that the compound shows fine multi-domains having fluidity. The lyotropic LC thus prepared displays smectic phase with layer structure.

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23

Thiruvalluvar, A., M. Subramanyam, R. T. Sabapathy Mohan, S. Kamatchi, and K. Murugavel. "3-Hydroxyimino-1-methyl-5-phenylcyclohexane-1-carbonitrile." Acta Crystallographica Section E Structure Reports Online 63, no. 6 (2007): o2780. http://dx.doi.org/10.1107/s1600536807020892.

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24

McIntosh, John M., E. Jay Kiser, and Zhigang Tian. "Article." Canadian Journal of Chemistry 76, no. 2 (1998): 147–51. http://dx.doi.org/10.1139/v97-223.

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Alkylation of the hippurate esters of trans 2-(p-substituted phenyl)cyclohexanol with benzyl bromide affords phenylalanine derivatives in high chemical yield. The reaction stereoselectivity varies from 20 to >98% depending on the aromatic group in the cyclohexyl auxiliary. A model that correctly predicts the sense of the induction is proposed.Key words: enolate conformation, pi-stacking, 2-phenylcyclohexanol, chiral auxiliary.

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25

Gao, Yan-qing, Shi-bin Shang, Jian Li, Xu Xu, and Xiao-ping Rao. "4-Isopropyl-N-phenylcyclohexa-1,3-diene-1-carboxamide." Acta Crystallographica Section E Structure Reports Online 66, no. 10 (2010): o2490. http://dx.doi.org/10.1107/s1600536810034859.

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26

Wallach, Jason, Giorgia De Paoli, Adeboye Adejare, and Simon D. Brandt. "Preparation and analytical characterization of 1-(1-phenylcyclohexyl)piperidine (PCP) and 1-(1-phenylcyclohexyl)pyrrolidine (PCPy) analogues." Drug Testing and Analysis 6, no. 7-8 (2013): 633–50. http://dx.doi.org/10.1002/dta.1468.

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27

Hartshorn, MP, WT Robinson, J. Vaughan, and JM White. "The Nitration of 4,6-Disubstituted 2-Phenylphenols. Some Structural Studies." Australian Journal of Chemistry 38, no. 4 (1985): 575. http://dx.doi.org/10.1071/ch9850575.

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Nitration of the bromophenols (4a) and (5a) give products of nitro-debromination . Reaction of 6-methyl-4-nitro-2-phenylphenol (5c) with nitrogen dioxide gives 2-hydroxy-2-phenylcyclohex-3-enones (8) and (9), and probably stereoisomers (10), (20), (21) and (22). The mode of ormation of these compounds is discussed. X-ray crystal structure determinations are reported for compounds (8) and (9).

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28

Singh, P., L. A. Jones, and R. Couch. "Stucture of 1-(1-phenylcyclohexyl)piperidine (PCP)." Acta Crystallographica Section C Crystal Structure Communications 44, no. 11 (1988): 1976–79. http://dx.doi.org/10.1107/s0108270188007206.

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29

Weidner, Karin, and Philippe Renaud. "Kinetic Study of the Radical Azidation with Sulfonyl Azides." Australian Journal of Chemistry 66, no. 3 (2013): 341. http://dx.doi.org/10.1071/ch12523.

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Rate constants for the reaction between a secondary alkyl radical and two different sulfonyl azides were determined using bimolecular competing radical reactions. The rates of azidation were determined by competition with hydrogen atom transfer from tris(trimethylsilyl)silane ((TMS)3SiH) of the 4-phenylcyclohexyl radical. 3-Pyridinesulfonyl azide and trifluoromethanesulfonyl azide were found to have rate constants for azidation of 2 × 105 M–1 s–1 and 7 × 105 M–1 s–1 at 80°C, respectively.

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30

Chang, N. L., V. M. Lynch, and S. H. Simonsen. "Tetrakis[1-(1-phenylcyclohexyl)piperidinium] Tetrachloromanganate(II) Dichloride." Acta Crystallographica Section C Crystal Structure Communications 54, no. 4 (1998): 475–76. http://dx.doi.org/10.1107/s0108270197005842.

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31

Luo, Xinxiang, and Zixing Shan. "2,4-Dibenzoyl-3,5-bis(4-methoxylphenyl)-1-phenylcyclohexanol." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1631—o1632. http://dx.doi.org/10.1107/s1600536806010634.

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The title compound, C40H36O5, was synthesized from p-anisaldehyde and acetophenone. The central six-membered ring adopts a chair conformation and most of the bulky side groups are located in equatorial positions. The hydroxyl group is involved in weak intra- and intermolecular hydrogen bonding.

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32

Karamysheva, L. A., K. V. Roitman, I. F. Agafonova, et al. "Liquid Crystalline Phenylcyclohexanes with A Lateral Methyl Substituent." Molecular Crystals and Liquid Crystals Incorporating Nonlinear Optics 191, no. 1 (1990): 259–67. http://dx.doi.org/10.1080/00268949008038603.

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33

MOORE, JOSEPH C. "Information on Nicotine Abuse." Pediatrics 86, no. 2 (1990): 329. http://dx.doi.org/10.1542/peds.86.2.329.

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To the Editor.— I would like to comment on some information offered in the Committee on Drugs' policy statement, "Transfer of Drugs and Other Chemicals into Human Milk", published in the November 1989 issue of Pediatrics.1 Nicotine is listed as a drug of abuse that is contraindicated during breast-feeding, in the same category as cocaine, heroin, marijuana, phencyclidine 1-(-1-phenylcyclohexyl) piperidine, and amphetamines. Three references are listed; however, none of them provide any good evidence to support a statement with such wide-ranging implications.

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34

Bochyński, Zenon, and Henryk Drozdowski. "X-ray diffraction studies of molecular correlations in liquid phenylcyclohexane." Journal of Molecular Liquids 80, no. 1 (1999): 53–63. http://dx.doi.org/10.1016/s0167-7322(98)00014-2.

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35

Ghani, Nurunajah Ab, Nor Hadiani Ismail, Yoshiaki Noma, and Yoshinori Asakawa. "Microbial Transformation of Some Natural and Synthetic Aromatic Compounds by Fungi: Aspergillus and Neurospora Strains." Natural Product Communications 12, no. 8 (2017): 1934578X1701200. http://dx.doi.org/10.1177/1934578x1701200822.

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Microbial transformation of chalcone (1), 4-hydroxychalcone (2) and 4′-hydroxychalcone (3), 1,1-diphenylmethane (4), 1,3-diphenylacetone (5), 1,3-diphenylpropane (6), bibenzyl (7), ( E)-stilbene (8a)- and ( Z)-stilbenes (8b), and phenylcyclohexane (9), (1 R,2 S)-1-phenyl-2-hydroxycyclohexane (9a) and (1 S,2 R)-1-phenyl-2-hydroxycyclohexane (9b), and a naturally occurring bis-bibenzyl, marchantin A (10) were performed by using Aspergillus niger TBUYN-2 and the other Aspergillus strains, and Neurospora crassa which were capable to hydrogenation and epoxidation of a conjugated double bond, and di

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36

Pancharoen, O., K. Picker, V. Reutrakul, WC Taylor, and P. Tuntiwachwuttikul. "Constituents of the Zingiberaceae. X. Diastereomers of [7-Hydroxy-5-Methoxy-2-Methyl-2-(4′-Methylpent-3′-Enyl)-2H-Chromen-8-yl] [3″-Methyl-2′-(3′″-Methylbut-2″′-Enyl]-6″-Phenylcyclohex-3″-Enyl]M Ethanone (Panduratin B), a Constituent of the Red Rhizomes of a Variety of Boesenbergia pandurata." Australian Journal of Chemistry 40, no. 3 (1987): 455. http://dx.doi.org/10.1071/ch9870455.

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Spectroscopic studies have established that panduratin B1 and panduratin B2, isolated from the red rhizomes of a variety of Boesenbergia pandurata ( Roxb .) Schltr ., are the diastereomers (2RS,1″ RS,2″SR,6″RS)- and (2RS,1″SR,2″RS,6″SR)-[7-hydroxy-5-methoxy-2-methyl-2-(4′-methylpent-3′-enyl)-2 H-chromen-8-yl][3″-methyl-2″-(3″′-methylbut-2″′-enyl)-6″-phenylcyclohex-3″-enyl]methanone. A synthesis of panduratin B mixture has been achieved by chromenylation of panduratin A.

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37

Bourke, DG, and DJ Collins. "Synthesis and Some Reactions of 1-(Trimethoxymethyl)cyclohexene." Australian Journal of Chemistry 49, no. 12 (1996): 1287. http://dx.doi.org/10.1071/ch9961287.

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1-( Trimethoxymethyl ) cyclohexene (11) was synthesized in three steps from N-methyl-N-phenylcyclohex-1-ene-1-carboxamide (8). Reaction of the α,β -unsaturated ortho ester (11) with sodium hydride and N- methylaniline gave a 1:1 mixture of methyl cyclohex-1-ene-1-carboxylate (15) and N,N- dimethylaniline . Treatment of (11) with 3-methoxyphenol gave 1-[ dimethoxy (3'-methoxyphenoxy)methyl] cyclohexene (10) which underwent thermolysis at 250° to give 1,3-dimethoxybenzene (16) and methyl cyclohex-1-ene-1-carboxylate (15).

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38

Parimal, K. Sen, Das Tulika, Maiti Krishnasri, Maiti Basudeb, and K. Sarkar Achintya. "Studies on alkylation of Hagemann's ester and its derivatives with alkyl halides and Michael acceptors." Journal of Indian Chemical Society Vol. 76, Nov-Dec 1999 (1999): 583–87. https://doi.org/10.5281/zenodo.5862213.

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Department of Chemistry, Presidency College, Calcutta-700 073, India <em>Manuscript received 25 August 1999</em> Alkylation and Michael addition of ethyl 3-methyl-4-oxo-2-phenylcyclohex-2-enecarboxylate (1b) have been studied under basic conditions. Similar reactions with Hagemann's ester (1c) have been carried out using phase transfer catalysts as well as solid supports. The ratio of the C-1 to C-3 alkylated products have been determined. A probable explanation for the regioselectivity observed has been given.

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39

Sathishkumar, Murugan, Sangaraiah Nagarajan, Poovan Shanmugavelan, Murugan Dinesh, and Alagusundaram Ponnuswamy. "A facile, rapid, one-pot regio/stereoselective synthesis of 2-iminothiazolidin-4-ones under solvent/scavenger-free conditions." Beilstein Journal of Organic Chemistry 9 (April 10, 2013): 689–97. http://dx.doi.org/10.3762/bjoc.9.78.

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A rapid and efficient one pot solvent/scavenger-free protocol for the synthesis of 2-iminothiazolidin-4-ones has been developed. Interestingly, the regio/stereoselective synthesis affords the regioisomeric (Z)-3-alkyl/aryl-2-(2-phenylcyclohex-2-enylimino)thiazolidin-4-one as the sole product in good yield. The selectivities observed have been rationalized based on the relative magnitude of the allylic strains developed during the course of the reaction. This is the first report wherein the impact of allylic strains in directing the regiocyclization has been noted.

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40

Navrátil, Oldřich, Zdeněk Skaličan, Zbyněk Kobliha, and Emil Halámek. "Competitive Extraction of Some Bases by Carbollylcobaltate Anion from Water Into Chloroform." Collection of Czechoslovak Chemical Communications 64, no. 7 (1999): 1111–18. http://dx.doi.org/10.1135/cccc19991111.

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The bis[undecahydro-7,8-dicarbaundecaborato(2-)]cobaltate(1-) (X-) has been used for complementary study of its ionic associates with some cations of organic bases and quaternary salts. For the optimization of present analytical methods, quinuclidin-3-yl hydroxy(diphenyl)acetate, 1-(1-phenylcyclohexyl)piperidine, dibenzo[b,f][1,4]oxazepine and cocaine, were studied by competitive extraction method. X- labelled with 60Co was used as carrier anion, triphenylmethane and azo dyes as competitive anions. The aqueous phase was 0.1 and 0.01 M HCl, the organic phase was chloroform. A comparison was mad

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41

Unett, David J., Richard A. Caldwell, and Duane C. Hrncir. "Photodimerization of 1-Phenylcyclohexene. A Novel Transient−Transient Component." Journal of the American Chemical Society 118, no. 7 (1996): 1682–89. http://dx.doi.org/10.1021/ja9533860.

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42

King, S. Bruce, and K. Barry Sharpless. "An efficient synthesis of enantiomerically pure trans-2-phenylcyclohexanol." Tetrahedron Letters 35, no. 31 (1994): 5611–12. http://dx.doi.org/10.1016/s0040-4039(00)77259-5.

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Beard, Richard L., Elliott S. Klein, Andrew M. Standeven, Maria Escobar, and Roshantha A. S. Chandraratna. "Phenylcyclohexene and phenylcyclohexadiene substituted compounds having retinoid antagonist activity." Bioorganic & Medicinal Chemistry Letters 11, no. 6 (2001): 765–68. http://dx.doi.org/10.1016/s0960-894x(01)00058-0.

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Chaturvedi, Arvind K., and David J. Kuntz. "Interaction between phencyclidine and its pyrolysis product, 1-phenylcyclohexene." Pharmacology Biochemistry and Behavior 30, no. 4 (1988): 1035–43. http://dx.doi.org/10.1016/0091-3057(88)90136-0.

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Carpenter, Bryon E., Ian R. Hunt, and Brian A. Keay. "A short efficient preparation of (+) and (−)-trans-2-phenylcyclohexanol." Tetrahedron: Asymmetry 7, no. 11 (1996): 3107–8. http://dx.doi.org/10.1016/0957-4166(96)00409-0.

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Cook, Michael J., and Khalida A. Nasri. "Conformational dependence of13C SCS in 1-methyl-1-phenylcyclohexanes." Magnetic Resonance in Chemistry 25, no. 7 (1987): 644–47. http://dx.doi.org/10.1002/mrc.1260250717.

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Sauer, Christoph, Frank T. Peters, Andrea E. Schwaninger, Markus R. Meyer, and Hans H. Maurer. "Identification of Cytochrome P450 Enzymes Involved in the Metabolism of the Designer DrugsN-(1-Phenylcyclohexyl)-3-ethoxypropanamine andN-(1-Phenylcyclohexyl)-3-methoxypropanamine." Chemical Research in Toxicology 21, no. 10 (2008): 1949–55. http://dx.doi.org/10.1021/tx8001302.

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Wang, Ya-Jun, Sheng-Liang Ni, and Yue Meng. "rac-syn-Diethyl 2-hydroxy-4-oxo-1-phenylcyclohexane-1,2-dicarboxylate." Acta Crystallographica Section E Structure Reports Online 67, no. 11 (2011): o2977—o2978. http://dx.doi.org/10.1107/s1600536811042048.

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Fun, Hoong-Kun, Madhukar Hemamalini, Mahesh Padaki, and Arun M. Isloor. "Diethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate." Acta Crystallographica Section E Structure Reports Online 66, no. 8 (2010): o1910. http://dx.doi.org/10.1107/s1600536810025018.

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Kakou-Yao, R., and J. P. Aycard. "Crystal structure of (6-phenylcyclohex-3-enyl)methanol, C13H16O." Zeitschrift für Kristallographie - New Crystal Structures 215, no. 4 (2000): 569–70. http://dx.doi.org/10.1515/ncrs-2000-0448.

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