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Journal articles on the topic 'N-phenylmorpholine'

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Author: Grafiati
Published: 9 March 2023
Last updated: 10 March 2023

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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 (December 24, 2010): o225. http://dx.doi.org/10.1107/s1600536810052207.

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2

Loghina, Liudmila, Anastasia Kaderavkova, Maksym Chylii, Bozena Frumarova, Petr Svec, Stanislav Slang, and Miroslav Vlcek. "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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3

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 (December 1992): 107–20. http://dx.doi.org/10.1080/10426509208034437.

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4

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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5

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 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199326088.

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6

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 (September 2012): 8267–75. http://dx.doi.org/10.1016/j.tet.2012.07.055.

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7

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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8

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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9

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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10

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 (May 1998): 1483–87. http://dx.doi.org/10.1016/s0957-4166(98)00095-0.

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11

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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Abstract:
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 accomplished. The reaction of Nsubistituted-2-(N-phenylmorpholine)ethylidene)hydrazine-1-carbothioamide (thiosemicarbazone derivative) with acetyl and ester-hydrazonoyl chlorides, α-chloroketones, or α-bromoesters afforded the corresponding thiazole derivatives pendent to N-phenylmorpholine moiety in good to excellent yields. Result: Mass, 1 H NMR, 13C NMR, and elemental analysis were used to confirm the structure of all the new derivatives. The antitumor activities of synthesized Nphenylmorpholine-thiazole derivatives were investigated against three tumor cells namely, TK-10, MCF-7 and UACC-62. The results of such investigation indicated that some derivatives showed good potential to inhibit the growth of the two cells of the tested tumor cells. Surprise, one of the tested compounds, N-methyl thiosemicarbazone derivative 7 revealed potent growth inhibition of all the three tumor cells. Conclusion: We have succeeded to synthesize a series of Nphenylmorpholine derivatives pendant to thiazole moiety as antitumor agents.
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12

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

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13

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 (January 1, 2012). http://dx.doi.org/10.1524/ncrs.2012.0047.

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14

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 (January 1, 2012). http://dx.doi.org/10.1524/ncrs.2012.0090.

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15

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 (January 6, 2009). http://dx.doi.org/10.1002/chin.200901176.

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