Academic literature on the topic 'N-phenylmorpholine'

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Journal articles on the topic "N-phenylmorpholine"

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Meng, Shuang-Ming, Ke-Wei Wang, Hai Xie, Yue-Qin Fan, and Yong Guo. "N-Phenylmorpholine-4-carboxamide." Acta Crystallographica Section E Structure Reports Online 67, no. 1 (2010): o225. http://dx.doi.org/10.1107/s1600536810052207.

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Loghina, Liudmila, Anastasia Kaderavkova, Maksym Chylii, et al. "The systematic study of the precursor ratio effect in the Cd–Zn–S quantum dot synthesis." CrystEngComm 22, no. 25 (2020): 4324–37. http://dx.doi.org/10.1039/d0ce00597e.

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Oladipo, S. D., N. O. Obi-Egbedi, M. D. Adeoye, N. D. Ojo, and A. A. Badeji. "Studies on the effect of solvents on the electronic absorption spectra of 4-phenylmorpholine and 1-phenylpyrrole." Scientia Africana 22, no. 1 (2023): 243–54. http://dx.doi.org/10.4314/sa.v22i1.21.

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The Ultraviolet-Visible (UV) spectra of 4-phenylmorpholine and 1-phenylpyrrole in different solvents have been studied. The molar absorptivities and oscillator strengths were determined. Also, quantum chemical calculations were carried out using time-dependent density functional theory with Beck-3-Lee-Yang-Parr exchange-correlation functional with a 6-31G* basis set (TDDFT/B3LYP/6- 31G*) for the optimized structures of the compounds. On the basis of this, the dipole moment, dihedral angle, oscillator strength, and singlet excited state of these compounds were determined in different solvents o
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Cremlyn, Richard J., Jatinder P. Bassin, Sultan Farouk, Michael Potterton, and Tajinder Mattu. "CHLOROSULFONATION OF N-PHENYLMORPHOLINE, BENZOTHIAZOLE, 2-METHYL BENZOTHIAZOLE AND TRIPHENYLOXAZOLE." Phosphorus, Sulfur, and Silicon and the Related Elements 73, no. 1-4 (1992): 107–20. http://dx.doi.org/10.1080/10426509208034437.

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Al-Soliemy, Amerah M. "Synthesis of Thiazolyl-N-phenylmorpholine Derivatives and their Biological Activities." Medicinal Chemistry 17, no. 7 (2021): 790–805. http://dx.doi.org/10.2174/18756638mta2anjkk1.

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CREMLYN, R. J., J. P. BASSIN, S. FAROUK, M. POTTERTON, and T. MATTU. "ChemInform Abstract: Chlorosulfonation of N-Phenylmorpholine, Benzothiazole, 2- Methylbenzothiazole and Triphenyloxazole." ChemInform 24, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199326088.

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Suarez-Bertoa, Ricardo, Francesco Saliu, Maurizio Bruschi, and Bruno Rindone. "Reaction products and mechanism of the regioselective oxidation of N-phenylmorpholine by ozone." Tetrahedron 68, no. 39 (2012): 8267–75. http://dx.doi.org/10.1016/j.tet.2012.07.055.

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Farghaly, Thoraya A., Alaa M. Abo Alnaja, Hoda A. El-Ghamry, and Mohamed R. Shaaban. "Synthesis and DNA binding of novel bioactive thiazole derivatives pendent to N-phenylmorpholine moiety." Bioorganic Chemistry 102 (September 2020): 104103. http://dx.doi.org/10.1016/j.bioorg.2020.104103.

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Kinzyabaeva, Z. S., and Z. N. Fazletdinova. "Synthesis of N-Substituted Morpholine C60-Fullerene Adducts in the Presence of LiOH and Lead(IV) Acetate." Журнал общей химии 93, no. 7 (2023): 995–1000. http://dx.doi.org/10.31857/s0044460x23070028.

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A N -phenyl-substituted morpholine adduct of C60 fullerene, 1,9-[4′-phenylmorpholine]-1,9-dihydro-(C60-Ih) [5,6]fullerene, was obtained for the first time with a yield of 56% in the reaction of 2-phenylaminoethanol with fullerene in the presence of LiOH and Pb(OAc)4 at room temperature for 1 h. The amino alcohol with an electron donor group (2-methylaminoethanol) in the reaction with fullerene showed a higher reactivity: the product 1,9-[4′-methylmorpholine]-1,9-dihydro-(С60-Ih)[5,6]fullerene was isolated in 68% yield. The presence of electron-withdrawing groups at the α- or β-carbon atom rela
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Al-Halbosy, Ahmed T. F., Adnan A. Hamada, Ahmed S. Faihan, et al. "Thiourea Derivative Metal Complexes: Spectroscopic, Anti-Microbial Evaluation, ADMET, Toxicity, and Molecular Docking Studies." Inorganics 11, no. 10 (2023): 390. http://dx.doi.org/10.3390/inorganics11100390.

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The treatment of N-Phenylmorpholine-4-carbothioamide (HPMCT) with bivalent metal ions in a 2:1 mol ratio without a base present affords [MCl2(κ1S-HPMCT)2] {M = Cu(1), Pd(2), Pt(3), and Hg(4)} in a good yield. Furthermore, the reaction of two equivalents of HPMCT and one equivalent of bivalent metal ions in the presence of Et3N has afforded [M(κ2S,N-PMCT)2] {M = Ni(5), Cu(6), Pd(7), Pt(8), Zn(9), Cd(10), and Hg(11)}. Infrared, 1H, 13C Nuclear Magnetic Resonance molar conductivity, and elemental analysis were used to characterize the synthesized complexes. The results suggest that HPMCT is bonde
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Dissertations / Theses on the topic "N-phenylmorpholine"

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SUAREZ, BERTOA RICARDO. "Sustainable procedures in organic synthesis." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2009. http://hdl.handle.net/10281/7474.

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O-acyl-N-benzyllactamides are obtained in good yield by reaction of 4-benzyl-5-methyl-1,3-oxazolidine-2,4-diones with Grignards reagents and with lithium alkyls. Three alkanes and two ethers were oxidised with ozone in dichloromethane solution or in aqueous pH 3 suspension. Cyclodecane and cyclododecane were converted into the corresponding cycloalkanones. n-decane was converted into a mixture of isomeric n-decanones and carboxylic acids. An ester was formed from the ethers. Hence, one of the methylene groups of these substrates is generally converted into a carbonyl group. Some of these react
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