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Relevant bibliographies by topics / 2-methoxynaphthalene

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Academic literature on the topic '2-methoxynaphthalene'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "2-methoxynaphthalene"

1

Nayak, Prakash S., Badiadka Narayana, Hemmige S. Yathirajan, Eric C. Hosten, Richard Betz, and Christopher Glidewell. "(2E)-3-(6-Methoxynaphthalen-2-yl)-1-(pyridin-3-yl)prop-2-en-1-one and its cyclocondensation product with guanidine, (4RS)-2-amino-4-(6-methoxynaphthalen-2-yl)-6-(pyridin-3-yl)-3,4-dihydropyrimidine monohydrate: two types of hydrogen-bonded sheet." Acta Crystallographica Section C Structural Chemistry 70, no. 11 (2014): 1011–16. http://dx.doi.org/10.1107/s2053229614021524.

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The structures of a chalcone and of its cyclocondensation product with guanidine are reported. In (2E)-3-(6-methoxynaphthalen-2-yl)-1-(pyridin-3-yl)prop-2-en-1-one, C19H15NO2, (I), the planes of the pyridine and naphthalene units make dihedral angles with that of the central spacer unit of 23.61 (13) and 23.57 (15)°, respectively, and a dihedral angle of 47.24 (9)° with each other. The molecules of (I) are linked into sheets by a combination of C—H...O and C—H...π(arene) hydrogen bonds. In the cyclocondensation product (4RS)-2-amino-4-(6-methoxynaphthalen-2-yl)-6-(pyridin-3-yl)-3,4-dihydropyri

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2

Tang, Chunbao. "2-Methoxynaphthalene-1-carbaldehyde." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (2009): o1088. http://dx.doi.org/10.1107/s1600536809014287.

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3

Bolte, M., and C. Bauch. "2-Methoxynaphthalene at 173K." Acta Crystallographica Section C Crystal Structure Communications 54, no. 12 (1998): 1862–63. http://dx.doi.org/10.1107/s0108270198009330.

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4

Balo, C., F. Fernández, E. Lens, and C. López. "ADIPOYLATION OF 2-METHOXYNAPHTHALENE." Organic Preparations and Procedures International 29, no. 2 (1997): 201–5. http://dx.doi.org/10.1080/00304949709355184.

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5

Prince, P., F. R. Fronczek, and R. D. Gandour. "2-Acetoxy-7-methoxynaphthalene." Acta Crystallographica Section C Crystal Structure Communications 50, no. 5 (1994): 797–98. http://dx.doi.org/10.1107/s0108270193010194.

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6

Jin, Bo, Zhong-Cheng Song, Fu-Sheng Jiang, Wen-Hong Liu, and Zhi-Shan Ding. "2-Methoxynaphthalene-1,4-dione." Acta Crystallographica Section E Structure Reports Online 67, no. 4 (2011): o947. http://dx.doi.org/10.1107/s1600536811009883.

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7

Bell, KH, and LF Mccaffery. "Use of Menthyl 2-Methoxynaphthalene-1-sulfinates in the Andersen Synthesis of Optically Active Sulfoxides. Facile Cleavage by Grignard Reagents of Some Aromatic Methyl Ethers." Australian Journal of Chemistry 47, no. 10 (1994): 1925. http://dx.doi.org/10.1071/ch9941925.

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The pure crystalline diastereomers (1R,2S,5R)-menthyl (R)- and (S)-2-methoxynaphthalene-1-sulfinate (1b) have been prepared and, by reaction with Grignard reagents (the Andersen procedure), converted into optically active alkyl and aryl 2-methoxynaphthyl sulfoxides in 67-77% yields. Use of an excess of Grignard reagent results in facile O-alkyl cleavage of the methoxy group to the corresponding naphthol or a competing loss of the alkyl- or aryl- sulfinyl group to form 2-methoxynaphthalene. Pure diastereomers of menthyl 2,7- dimethoxynaphthalene-1-sulfinate (2b) and menthyl 4-methoxynaphthalene

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8

Meana-Esteban, B., C. Kvarnström, B. Geschke, J. Heinze, and A. Ivaska. "Electrochemical polymerization of 2-methoxynaphthalene." Synthetic Metals 139, no. 1 (2003): 133–43. http://dx.doi.org/10.1016/s0379-6779(03)00079-1.

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9

Kim, Sung Duk, Kyung Hee Lee, Jae Sung Lee, Young Gul Kim, and Kwang Eui Yoon. "The regioselective acylation of 2-methoxynaphthalene to 2-acetyl-6-methoxynaphthalene over zeolite beta." Journal of Molecular Catalysis A: Chemical 152, no. 1-2 (2000): 33–45. http://dx.doi.org/10.1016/s1381-1169(99)00266-6.

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10

Harvey, Gillian, and Georg Mäder. "The Shape-Selective Acylation of 2-Methoxynaphthalene, Catalyzed by Zeolites Y, Beta and ZSM-12." Collection of Czechoslovak Chemical Communications 57, no. 4 (1992): 862–68. http://dx.doi.org/10.1135/cccc19920862.

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The Friedel-Crafts acylation of 2-methoxynaphthalene (2MN) was investigated using zeolites USY, Beta and ZSM-12 as catalysts under batch conditions at 100 and 180 °C. Two ketone isomers, 1-acetyl-2-methoxynaphthalene (1AC) and 2-acetyl-6-methoxynaphthalene (2AC) were produced; the selectivity of the reaction could be influenced by the zeolite used. USY produced only the 1AC isomer whereas Beta and ZSM-12 produced both. Selective synthesis of 2AC was achieved by optimization of the reaction conditions using zeolite Beta as the catalyst. It was also observed that the 1AC ketone is unstable in co

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Dissertations / Theses on the topic "2-methoxynaphthalene"

1

Kantarlı, İsmail Cem Artok Levent. "Acylation of 2-Methoxynaphthalene Over Ion-Exchanged Beta Zeolite/." [s.l.]: [s.n.], 2002. http://library.iyte.edu.tr/tezler/master/kimya/T000142.pdf.

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2

Swigelaar, Wendell Peter. "The synthesis of 3-allyl-4-ethyl-2- (1'-hydroxyethyl)-1-methoxynaphthalene and its behaviour towards base- and palladium-promoted cyclisation under aerobic and anaerobic conditions." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&amp.

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Over the years, Giles and co-workers have established that, upon treatment with potassium tert-butoxide, tetra-substituted naphthalenes undergo cyclisations to afford naphthopyrans. It was suggested that these base-induced cyclisations was as a result of the reacting centers being forced into close proximity as a consequence of steric crowding.<br /> <br /> This thesis describes the synthesis of 3-allyl-4-ethyl-2-(1&prime<br>-hydroxyethyl)-1-methoxy-naphthalene 177 and its behaviour towards Pd(0) and potassium tert-butoxide under aerobic and anaerobic conditions, to verify whether the base-pro

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Book chapters on the topic "2-methoxynaphthalene"

1

Kantarli, I. C., L. Artok, H. Bulut, S. Yilmaz, and S. Ülkü. "Acylation of 2-methoxynaphthalene over ion-exchanged β-zeolite." In Studies in Surface Science and Catalysis. Elsevier, 2002. http://dx.doi.org/10.1016/s0167-2991(02)80104-5.

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2

Moreau, V., E. Fromentin, P. Magnoux, and M. Guisnet. "25-P-08-1-acetyl-2-methoxynaphthalene isomerization over zeolites. Effect of pore structure." In Studies in Surface Science and Catalysis. Elsevier, 2001. http://dx.doi.org/10.1016/s0167-2991(01)81616-5.

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3

Liao, C. C., and R. K. Peddinti. "Oxidation of a 1-Methoxynaphthalen-2-amine Derivative." In Quinones and Heteroatom Analogues. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-028-00301.

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