Relevant bibliographies by topics / Methyl-2-naphthyl ether

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  1. Journal articles

Academic literature on the topic 'Methyl-2-naphthyl ether'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Methyl-2-naphthyl ether"

1

Németh, Tamás, Tünde Tóth, György Tibor Balogh, and Péter Huszthy. "Synthesis and Fluorescence Spectroscopic Studies of Novel 9-phenylacridino-18-crown-6 Ether Type Sensor Molecules." Periodica Polytechnica Chemical Engineering 61, no. 4 (2017): 249. http://dx.doi.org/10.3311/ppch.11277.

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The synthesis of two new 9-phenylacridino-18-crown-6 ether type sensor molecules [1 and (R,R)-2] was accomplished. The cation recognition ability of the achiral sensor molecule 1 towards various ions was studied in acetonitrile by UV/Vis and fluorescence spectroscopies. Our studies revealed the binding of Ag+, Cd2+, Ni2+, Pb2+, Zn2+ and NH4+ ions by the latter molecule. Selectivity of the chiral dimethyl-substituted analogue (R,R)-2 was studied toward the enantiomers of the hydrogen perchlorate salts of 1-phenylethylamine, 1-(1-naphthyl)ethylamine, phenylglycine methyl ester and phenylalanine
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2

Himbert, Gerhard, Dieter Fink, and Martina Stürm. "Cycloadditionen, XXI [1]. 2-Methyl-2,3-butadiensäure-arylester; Synthese und thermische Reaktivität / Cycloadditions, XXI [1] Aryl 2-methyl-2,3-butadienoates; Synthesis and Thermal Reactivity." Zeitschrift für Naturforschung B 49, no. 1 (1994): 63–75. http://dx.doi.org/10.1515/znb-1994-0114.

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Abstract The substituted phenyl, 1-naphthyl or the 9-anthrylmethyl esters of the 2-methyl-(or 2-phenyl)-2,3-alkadienoic acids (see 4 a -g , 9 a -d and 12a,b) are synthesized by condensation of the allenic acids 2 a -d with the substituted phenols 3 a -g , with 1-naphthol (8) or with 9-anthrylmethanol (11) in the presence of dicyclohexyl carbodiimide (DCC) and a catalytic amount of 4-dimethylaminopyridine (DMAP). An alternative route is the reaction of the acid chloride la with the phenols 3 a -c (see formation of 4 a -c) in the presence of triethylamine. All these compounds (except 12a) underg
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3

Li, Xiao-Fang, Ya-Qing Feng, Xiao-Fen Hu, and Guan Wang. "1-Benzyl-5-(1-naphthylmethylene)piperidinespiro-3,3′-1′-methyl-4′-(1-naphthyl)pyrrolidinespiro-2′,3′′-indole-2′′,4-dione–diethyl ether (1/0.75)." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): o1025—o1027. http://dx.doi.org/10.1107/s1600536803013825.

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4

Jotani, Mukesh M., P. Iniyavan, V. Vijayakumar, S. Sarveswari, Yee Seng Tan, and Edward R. T. Tiekink. "12-(3,4,5-Trimethoxyphenyl)-2,3,4,12-tetrahydro-1H-5-oxatetraphen-1-one: crystal structure and Hirshfeld surface analysis." Acta Crystallographica Section E Crystallographic Communications 72, no. 6 (2016): 809–14. http://dx.doi.org/10.1107/s2056989016007775.

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In the title compound, C26H24O5, the pyran ring has a flattened-boat conformation, with the 1,4-related ether O and methine C atoms lying 0.1205 (18) and 0.271 (2) Å, respectively, above the least-squares plane involving the doubly bonded C atoms (r.m.s deviation = 0.0208 Å). An envelope conformation is found for the cyclohexene ring, with the flap atom being the middle methylene C atom, lying 0.616 (2) Å out of the plane defined by the remaining atoms (r.m.s. deviation = 0.0173 Å). The fused four-ring system is approximately planar, with the dihedral angle between the least-squares planes thr
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5

Szabó, Zoltán B., Anikó Borbás, István Bajza та András Lipták. "Synthesis of fully protected α-l-fucopyranosyl-(1→2)-β-d-galactopyranosides with a single free hydroxy group at position 2′, 3′ or 4′ using O-(2-naphthyl)methyl (NAP) ether as a temporary protecting group". Tetrahedron: Asymmetry 16, № 1 (2005): 83–95. http://dx.doi.org/10.1016/j.tetasy.2004.11.056.

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6

Lee, B. Y., P. H. Seeberger, and D. Varon Silva. "Synthesis of glycosylphosphatidylinositol (GPI)-anchor glycolipids bearing unsaturated lipids." Chemical Communications 52, no. 8 (2016): 1586–89. http://dx.doi.org/10.1039/c5cc07694c.

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A new strategy involving 2-naphthyl-methyl ethers as permanent protecting groups and their easy removal under acidic conditions is the key to the synthesis of complex glycosylphosphatidylinositol glycolipids containing unsaturated lipids.
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7

Pál, Dávid, Martin Gede, Ildikó Móczár, Péter Baranyai, Péter Bagi, and Péter Huszthy. "Synthesis and Complexation Studies of Optically Active Aza- and Diazacrown Ethers Containing a Pyrene Fluorophore Unit." Periodica Polytechnica Chemical Engineering 64, no. 1 (2019): 20–36. http://dx.doi.org/10.3311/ppch.14467.

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Novel enantiopure azacrown [(R,R)-1 and (S,S)-1] and diazacrown [(R,R)-2–(R,R)-4 and (S,S)-2–(S,S)-4] ethers containing a pyrene fluorophore unit and two phenyl groups at their chiral centers were obtained in multistep syntheses. The action of these chemosensors is based on the photoinduced electron transfer (PET) process, thus they show fluorescence enhancement in the presence of protonated primary amines and amino acid esters. Their recognition abilities toward the enantiomers of 1-phenylethylamine hydrogen perchlorate (PEA), 1-(1-naphthyl) ethylamine hydrogen perchlorate (NEA), phenylglycin
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8

Borbás, Anikó, Zoltán B. Szabó, László Szilágyi, Attila Bényei, and András Lipták. "Dioxane-type (2-naphthyl)methylene acetals of glycosides and their hydrogenolytic transformation into 6-O- and 4-O-(2-naphthyl)methyl (NAP) ethers." Tetrahedron 58, no. 28 (2002): 5723–32. http://dx.doi.org/10.1016/s0040-4020(02)00515-x.

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9

Csávás, Magdolna, Anikó Borbás, László Szilágyi, and András Lipták. "Successful Combination of (Methoxydimethyl)methyl (MIP) and (2-Naphthyl)methyl (NAP) Ethers for the Synthesis of Arabinogalactan-Type Oligosaccharides." Synlett 2002, no. 06 (2002): 0887–90. http://dx.doi.org/10.1055/s-2002-31893.

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10

Rehan, Hyman H. "Electrosynthesis and characterization of new conducting copolymer films from 1-naphthol and methyl naphthyl ether." Polymer International 49, no. 7 (2000): 645–53. http://dx.doi.org/10.1002/1097-0126(200007)49:7<645::aid-pi368>3.0.co;2-o.

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