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Articles de revues sur le sujet « N-phenylmorpholine »

Auteur : Grafiati
Publié le 9 mars 2023
Mis à jour le 31 juillet 2025

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1

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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11

Hallas, Geoffrey, Richard Marsden, John D. Hepworth, and Donald Mason. "The effects of cyclic terminal groups in 4-aminoazobenzene and related azo dyes. Part 3. Electronic absorption spectra of some monoazo dyes derived from N-phenylmorpholine, N-(phenyl)thiomorpholine, N-(phenyl)thiomorpholine 1,1-dioxide, and N-acetyl-N′-phenylpiperazine." J. Chem. Soc., Perkin Trans. 2, no. 1 (1986): 123–26. http://dx.doi.org/10.1039/p29860000123.

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12

Aldous, David J., Estelle M. N. Hamelin, Laurence M. Harwood, and Sukanthini Thurairatnam. "N-(1′-Benzotriazolylmethyl)-5-phenylmorpholin-2-one: A Stable Crystalline Chiral Azomethine Ylid Precursor." Synlett 2001, no. 12 (2001): 1841–42. http://dx.doi.org/10.1055/s-2001-18763.

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13

Bull, Steven D., Stephen G. Davies, David J. Fox, and Thomas G. R. Sellers. "Chiral relay effects influence the facial selectivity of N-alkylated 5-phenylmorpholin-2-one enolates." Tetrahedron: Asymmetry 9, no. 9 (1998): 1483–87. http://dx.doi.org/10.1016/s0957-4166(98)00095-0.

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14

Al-Soliemy, AM. "Synthesis of Thiazolyl-N-phenylmorpholine Derivatives and their Biological Activities." Medicinal Chemistry 17, no. 7 (2021). http://dx.doi.org/10.2174/15734064mta2jnjkr1.

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Al-Soliemy, Amerah M., Thoraya A. Farghaly, Eman M. H. Abbas, Mohamed R. Shaaban, Mohie E. M. Zayed, and Tarek B. A. El-Naggar. "Synthesis of thiazolyl-N-phenylmorpholine derivatives and their biological activities." Medicinal Chemistry 16 (May 17, 2020). http://dx.doi.org/10.2174/1573406416666200517103435.

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Background: Morpholine and thiazole rings are two heterocycles which well-known with wide spectrum of different biological activities especially antitumor activity. Objective: The aim of the work is to design and synthesis hybrid heterocyclic compounds of morpholine and thiazole moieties via the reaction of morpholino-thiosemicarbazone derivatives with various αhalocarbonyl compounds and screening their antitumor activity against three tumor cell lines namely, TK-10, MCF-7 and UACC-62. Method: An efficient synthesis of a series of Nphenylmorpholine derivatives linked with thiazole moiety were
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16

Balu, Ranjith, Anthoniammal Panneerselvam, Gautham Devendrapandi, Jothi Ramalingam Rajabathar, Hamad A. Al-lohedan, and Dhaifallah M. Al-dhayan. "Theoretical and experimental spectroscopic studies and analysis for wave function on N-phenylmorpholine-4-carboxamide benzene-1,2-diamine with computational techniques." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, June 2023, 122988. http://dx.doi.org/10.1016/j.saa.2023.122988.

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17

Chen, Min-Dong, Bo Xiao, and Xuan Gong. "Crystal structure of N-propynoyl-(5R)- 5-phenylmorpholin-2-one, C13H11NO3." Zeitschrift für Kristallographie - New Crystal Structures 227, no. 2 (2012). http://dx.doi.org/10.1524/ncrs.2012.0047.

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Chen, Min-Dong, Junfeng Wang, Bo Xiao, and Xuan Gong. "Crystal structure of N-propynoyl-(5R)-3-methyl- 5-phenylmorpholin-2-one, C14H13NO3." Zeitschrift für Kristallographie - New Crystal Structures 227, no. 2 (2012). http://dx.doi.org/10.1524/ncrs.2012.0090.

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Chen, Mindong, Yu Gan, and Laurence M. Harwood. "ChemInform Abstract: Azide 1,3-Dipolar Cycloadditions to N-Propynoyl and N-Propenoyl (5R)-5-Phenylmorpholin-2-one: Diastereocontrolled Aziridine Formation." ChemInform 40, no. 1 (2009). http://dx.doi.org/10.1002/chin.200901176.

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