Relevant bibliographies by topics / Tetrahydronaphthalene

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

Academic literature on the topic 'Tetrahydronaphthalene'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Tetrahydronaphthalene"

1

Collins, DJ, JD Cullen, and GM Stone. "The Structure and Function of Estrogens .10. Synthesis of 5,5-Dimethyl-Cis-4b,5,6,10b,11,12-Hexahydrochrysene-2,8-Diol - the Estrogenic Activity of This and of Related C-Methylated Hydrochrysenediols." Australian Journal of Chemistry 41, no. 5 (1988): 745. http://dx.doi.org/10.1071/ch9880745.

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Reaction of 6-methoxy-2-(p- methoxyphenyl )-3,4-dihydronaphthalen-1(2H)- one (9) with dimethylketene ethyl trimethylsilyl acetal (10) in the presence of titanium tetrachloride gave ethyl 2-methyl-2-[6?-methoxy- 2?-(p- methoxyphenyl )-3?,4?-dihydronaphthalen-1?-yl] propanoate (11) which upon treatment with methanesulfonic acid afforded the lactone (13). Reduction of (11) with lithium/ammonia yielded mainly 6-methoxy- 2-(p- methoxyphenyl )-1,2,3,4-tetrahydronaphthalene (16), but hydrogenation of (11) over palladium/charcoal gave 61% of ethyl (1?RS,2?RS)-2-methyl-2-[6?-methoxy-2?-(p- methoxypheny
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2

Çakmak, Osman, Ismail Kahveci, Íbrahim Demirtaş, Tuncer Hökelek, and Keith Smith. "Bromination of Tetralin. Short and Efficient Synthesis of 1,4-Dibromonaphthalene." Collection of Czechoslovak Chemical Communications 65, no. 11 (2000): 1791–804. http://dx.doi.org/10.1135/cccc20001791.

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High-temperature bromination of tetralin (1,2,3,4-tetrahydronaphthalene) with bromine resulted in benzylic bromination to give 1,4-dibromo-1,2,3,4-tetrahydronaphthalene (4) as a major product and several secondary products. Photolytic bromination of tetralin and subsequent double dehydrobromination of 1,1,4,4-tetrabromo-1,2,3,4-tetrahydronaphthalene (10) gave 1,4-dibromonaphthalene (11) as the sole product in a high yield. 1,4-Dibromonaphthalene is efficiently converted to the corresponding methoxy (12 and 13) and cyano (14 and 15) derivatives of naphthalene.
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3

Kasai, Masaji, Herman Ziffer, and J. V. Silverton. "Enantioselective ester hydrolyses using Rhizopusnigricans: stereoselective synthesis and absolute stereochemistry of (−)-cis- and (−)-trans-1-hydroxy-4-methyl-1,2,3,4-tetrahydronaphthalene." Canadian Journal of Chemistry 63, no. 6 (1985): 1287–91. http://dx.doi.org/10.1139/v85-219.

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Enantioselective hydrolysis of racemic acetates of cis- and trans-1-hydroxy-4-methyl-1,2,3,4-tetrahydronaphthalene using Rhizopusnigricans yields chiral alcohols. The absolutestereochemistry of these compounds, and that of a key intermediate in their stereoselective synthesis, r-1-hydroxy-2,t-bromo-4,c-methyl-1,2,3,4-tetrahydronaphthalene, were determined by chemical transformations to 1-oxo-4-methyl-1,2,3,4-tetrahydronaphthalene of known absolute stereochemistry. The relativestereochemistry of the acetate of the key intermediate was established by X-ray crystallography.
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4

ROWE, F. M. "Some New Tetrahydronaphthalene Derivatives and Dyestuffs obtained from Tetrahydronaphthalene Derivatives.*." Journal of the Society of Dyers and Colourists 35, no. 5 (2008): 128–34. http://dx.doi.org/10.1111/j.1478-4408.1919.tb01058.x.

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5

Beckwith, PLM, EL Ghisalberti, PR Jefferies, CL Raston, and AH White. "A Study of the Photochemistry of Benzobicyclo[2.2.2]octan-2-ones." Australian Journal of Chemistry 41, no. 3 (1988): 351. http://dx.doi.org/10.1071/ch9880351.

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The anti- and syn-3-methyl isomers of 5,8-dimethoxy-1,3-dimethyl-3,4-dihydro-1,4-ethanonaphthalen-2(1H)-one (2) and (3) and the 1,3,3- trimethyl analogue (4) were prepared from the Diels -Alder adduct of benzoquinone and 1,3-dimethylcyclohexadiene. The photochemistry of each has been studied and the structures of several photoproducts have been assigned. One of the products from irradiation of (3) was found by X-ray analysis to be a 1,4-disubstituted 1,2,3,4- tetrahydronaphthalene [methyl 2-(5′,8′-dimethoxy-4z′-methyl-1′,2′,3′,4′-tetrahydronaphthalen-1′-yl) propanoate ] with the unexpected cis
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6

Kudavalli, Jaya S., та Rory A. More O'Ferrall. "β-Hydroxy carbocation intermediates in solvolyses of di- and tetra-hydronaphthalene substrates". Beilstein Journal of Organic Chemistry 6 (3 листопада 2010): 1035–42. http://dx.doi.org/10.3762/bjoc.6.118.

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Solvolysis of trichloroacetate esters of 2-methoxy-1,2-dihydro-1-naphthols shows a remarkably large difference in rates between the cis and trans isomers, k cis /k trans = 1800 in aqueous acetonitrile. This mirrors the behaviour of the acid-catalysed dehydration of cis- and trans-naphthalene-1,2-dihydrodiols to form 2-naphthol, for which k cis /k trans = 440, but contrasts with that for solvolysis of tetrahydronaphthalene substrates, 1-chloro-2-hydroxy-1,2,3,4-tetrahydronaphthalenes, for which k cis /k trans = 0.5. Evidence is presented showing that the trans isomer of the dihydro substrates r
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7

Heine, Angelika. "Is tetrahydronaphthalene an allergen?" Contact Dermatitis 24, no. 4 (1991): 303. http://dx.doi.org/10.1111/j.1600-0536.1991.tb01729.x.

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8

Zou, Pei, Min-Hao Xie, Hao Wu, Ya-Ling Liu, and Yong-Jun He. "5,6,7,8-Tetrahydronaphthalene-1-carboxylic acid." Acta Crystallographica Section E Structure Reports Online 65, no. 12 (2009): o3223. http://dx.doi.org/10.1107/s1600536809049721.

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9

Ma, Eunsook, and Thi Nguyen. "Chemoselective Synthesis of N-(Aminoalkyl/amidino)phenyl Naphthalene-1-carboxamides and 5,6,7,8-Tetrahydronaphthalene-1-carboxamides and Their Anticoagulant Screening." Synlett 28, no. 19 (2017): 2660–64. http://dx.doi.org/10.1055/s-0036-1588517.

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N-[(Aminoalkyl)phenyl]-1-naphthamides and N-[(amino­alkyl)phenyl]-5,6,7,8-tetrahydronaphthalene-1-carboxamides were selectively synthesized from the corresponding cyanonaphthamides by catalytic hydrogenation. N-(Amidinophenyl)-1-naphthalenecarbox­amides and N-(amidinophenyl)-5,6,7,8-tetrahydronaphthalene-1-carboxamides were chemoselectively obtained from the corresponding O-acetylamidoximes or amidoximes, respectively, by catalytic hydrogenation. The products were screened for their anticoagulant effects in human plasma, as measured by the activated partial thromboplastin time and the prothrom
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10

Serra, Stefano. "Stereoselective Synthesis of 2,15-Dihydroxycalamenene and 2-Methoxycalamenene. Determination of the Configuration of Natural 2,15-Dihydroxycalamenene." Natural Product Communications 10, no. 8 (2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000803.

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The enantioselective preparation of the two diastereoisomeric forms of 2,15-dihydroxycalamele‘ne and 2-methoxycalamenene is here described. The (7 S,10 R) and (7 R,10 R) isomers of these natural products were synthesized starting from (5 R,8 S)-methyl-4-hydroxy-8-isopropyl-5-methyl-5,6,7,8-tetrahydronaphthalene-2-carboxylate and (5 R,8 R)-methyl-4-hydroxy-8-isopropyl-5-methyl-5,6,7,8-tetrahydronaphthalene-2-carboxylate, respectively, in turn preparable from (-)-menthone and (+)-isomenthone. The NMR analysis of the obtained sesquiterpenes allow assigning (7 R,10 S) absolute configuration to the
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Dissertations / Theses on the topic "Tetrahydronaphthalene"

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Arnold, Jennifer M. "Time course and regional specificity of neurochemical changes in the rat brain following intra-accumbal and intra-striatal injections of 6,7-ADTN (2-amino-6,7-dihydroxy-1,2,3-tetrahydronaphthalene)." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1996. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/MQ26532.pdf.

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Arnold, Jennifer M. "Time course and regional specificity of neurochemical changes in the rat brain following intra-accumbal and intra-striatal injections of 6,7-ADTN (2-amino-6,7-dihydroxy-1,2,3-tetrahydronaphthalene )." Sherbrooke : Université de Sherbrooke, 1997.

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3

Essien, Herbert Ebiom. "Synthesis And Opioid-Related Activities Of Some Cis - And Trans -3-(Mono- Or Dialkylamino)-7-(Methoxy Or Hydroxy)-1-Phenyl-1,2,3,4-Tetrahydronaphthalenes." Scholarly Commons, 1986. https://scholarlycommons.pacific.edu/uop_etds/3021.

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Cis and trans isomers of 3-(mono- or dialkylamino)-7-(methoxy or hydroxy)-1-phenyl-1,2,3,4-tetrahydronapthalenes were synthesized. Compounds HC- 11 (cis) and HT- 11 (trans) with 3- (dimethylamino) and 7-methoxy substituents and compounds HC- 13 and HT- 13 with 3- ((cyclopropylmethyl)methylamino) and 7-methoxy substituents were synthesized from their corresponding 3-(methylamino) and 7-methoxy derivatives (HC- 10 and HT- 10). HC- 10 and HT- 10 were previously prepared by reductive amination of the 3-tetralone and separated by fractional recrystallization. HC- 10 was obtained predominantly in a
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Makgato, Matlou Hector. "Effects of hydrogen donor additives on the coking properties of high temperature coal extracts." 2008. http://upetd.up.ac.za/thesis/available/etd-02092009-125239.

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5

Wei, Yu-Hsin, та 魏育信. "Stabilized Koopmans' Theorem Calculations on the π* Anion States of 1,4,5,8-Tetrahydronaphthalene and 1,,4,5,8,9,10-Hexahydro-Anthracene". Thesis, 1998. http://ndltd.ncl.edu.tw/handle/06926573282767444302.

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碩士<br>東海大學<br>應用化學系研究所<br>86<br>The exponent stabilized Koopmans' theorem is used to calculatethe energies of the π* anion states of 1,4,5,8-tetrahydronaphthalene(isotetralin). The results indicate that the ordering of π* anion statesis 2 B3g < 2 Au < 3B3g. This order of anion sataes is the same as that which would prevail were only through-space (TS) interactions present.The through-bond (TB) interactions destabilize all the π* orbitals;however, they do not change the order. The π* anion states of 1,4,5,8,9,10-hexahydro-anthracene (HHA)are also assigned by means of the exponent stabilized Ko
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Books on the topic "Tetrahydronaphthalene"

1

Tetrahydronaphthalene. S. Hirzel, 1994.

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2

Dourish, Colin T., and S. Ahlenius. Brain 5-Ht Receptors, 1A: Behavioural and Neurochemical Pharmacology (Ellis Horwood Series in Biomedicine). Vch Pub, 1988.

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Dourish, Colin T. Brain 5HT 1A Receptors. Wiley-VCH, 1987.

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4

T, Dourish Colin, Hutson P, and Ahlenius S, eds. Brain 5-HT[subscript]IA receptors: Behavioural and neurochemical pharmacology. VCH, 1987.

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T, Dourish Colin, Ahlenius Sven, and Hutson P, eds. Brain 5-HT1̳A̳ receptors: Behavioural and neurochemical pharmacology. VCH, 1987.

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Book chapters on the topic "Tetrahydronaphthalene"

1

Gooch, Jan W. "Tetrahydronaphthalene." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_11708.

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2

Wohlfarth, Ch. "Viscosity of 1,2,3,4-tetrahydronaphthalene." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_336.

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Wohlfarth, Christian. "Viscosity of 1,2,3,4-tetrahydronaphthalene." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_335.

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Wohlfarth, Ch. "Refractive index of 1,2,3,4-tetrahydronaphthalene." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_300.

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Wohlfarth, Ch. "Dielectric constant of 1,2,3,4-tetrahydronaphthalene." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_289.

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6

Wohlfarth, Christian. "Refractive index of 1,2,3,4-tetrahydronaphthalene." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_351.

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Wohlfarth, Ch. "Viscosity of the mixture (1) diisopropyl ether; (2) 1,2,3,4-tetrahydronaphthalene." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_1664.

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Wohlfarth, Ch. "Dielectric constant of the mixture (1) tribromomethane; (2) 1,2,3,4-tetrahydronaphthalene." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_411.

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Wohlfarth, Christian. "Refractive index of binary liquid mixture of octane and 1,2,3,4-tetrahydronaphthalene." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_1038.

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Wohlfarth, Christian. "Refractive index of binary liquid mixture of nonane and 1,2,3,4-tetrahydronaphthalene." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_1047.

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Conference papers on the topic "Tetrahydronaphthalene"

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Liu, Yuyan, Xianyun Gong, Songquan Wu, and Lan Li. "Decomposition of Epoxy Resin E-44/METHPA by Tetrahydronaphthalene." In 2012 International Conference on Biomedical Engineering and Biotechnology (iCBEB). IEEE, 2012. http://dx.doi.org/10.1109/icbeb.2012.124.

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Jaber, T. J., H. Bataller, and M. Z. Saghir. "Measurement of Thermodiffusion Coefficient for Binary Hydrocarbon Fluid Mixtures in Porous Medium: Experimental and Numerical Results." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-10110.

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There has been a discussion that the thermodiffusion in porous medium is not identical to thermodiffusion in clear liquid. To validate this finding, a new thermodiffusion cell has been designed to measure thermal and molecular diffusion coefficients of binary mixture in porous medium under high pressure. A porous layer located between two liquid layers that cross two laser beams, is used. The difference of refractive index is obtained from the analysis of the interferograms recorded with a CCD camera. From the kinetics, the values of molecular and thermal diffusion coefficients through the por
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