Academic literature on the topic '5- trimethoxyphenyl)-1'

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Journal articles on the topic "5- trimethoxyphenyl)-1"

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Pankaj, Yadav, and Kumar Goyal Pramod. "A Research On Unveiling Novel Chemotherapeutic Agents: Design, Synthesis, and Anticancer Evaluation of N-(Substituted Phenyl)-5-(3, 4, 5- Trimethoxyphenyl)-1, 3, 4-Oxadiazol-2-Amine Analogues." International Journal of Current Pharmaceutical Review and Research 16, no. 05 (2024): 79–94. https://doi.org/10.5281/zenodo.12785139.

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AbstractA Series of newer 5-substituent N-(substituent phenyl)-5-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazol-2-amineanalogues 4a-f was subjected to molecular properties prediction by mol soft and Molinspiration software andwas synthesized in satisfactory yields. All the compounds followed the Lipinski “rule of five “which makesthem potentially active agents. 3 Compound (4a, 4b & 4f) were evaluated for their anticancer activity in onedose assay and showed moderate activity on various cell lines. Compound N-(4-chlorophenyl)-5-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazol-2-amine (4b) sho
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Monroe, Thomas Blake, Casey Rimland, Yasamin Moazami, Daniel S. Jones, and Craig A. Ogle. "5-Methoxy-1-(3,4,5-trimethoxyphenyl)-1H-indole." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1678. http://dx.doi.org/10.1107/s1600536810018568.

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Twamley, Brendan, Niamh M. O'Boyle, and Mary J. Meegan. "Azetidin-2-ones: structures of antimitotic compounds based on the 1-(3,4,5-trimethoxyphenyl)azetidin-2-one core." Acta Crystallographica Section E Crystallographic Communications 76, no. 8 (2020): 1187–94. http://dx.doi.org/10.1107/s2056989020008555.

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A series of related substituted 1-(3,4,5-trimethoxyphenyl)azetidin-2-ones have been characterized: 3-(4-fluorophenyl)-4-(4-methoxyphenyl)-1-(3,4,5-trimethoxyphenyl)azetidin-2-one, C25H24FNO5 (1), 3-(furan-2-yl)-4-(4-methoxyphenyl)-1-(3,4,5-trimethoxyphenyl)azetidin-2-one, C23H23NO6 (2), 4-(4-methoxyphenyl)-3-(naphthalen-1-yl)-1-(3,4,5-trimethoxyphenyl)azetidin-2-one, C29H27NO5 (3), 3-(3,4-dimethoxyphenyl)-4-(4-methoxyphenyl)-1-(3,4,5-trimethoxyphenyl)azetidin-2-one, C27H29NO7 (4) and 4,4-bis(4-methoxyphenyl)-3-phenyl-1-(3,4,5-trimethoxyphenyl)azetidin-2-one, C32H31NO6 (5). All of the compounds
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Ban, Ninh Khac, Luu Hong Truong, Tran My Linh, et al. "Phenolic compounds from Trigonostemon honbaensis and their cytotoxic activity." Vietnam Journal of Chemistry 58, no. 6 (2020): 759–64. http://dx.doi.org/10.1002/vjch.202000068.

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AbstractSeven phenolic compounds including (±)‐erythro‐1‐(3′,4′,5′‐trimethoxyphenyl)propane‐1,2‐diol (1), (±)‐threo‐1‐(3′,4′,5′‐trimethoxyphenyl)propane‐1,2‐diol (2), (R)‐3‐3‐(3′,4′‐dimethoxyphenyl)propane‐1,2‐diol (3), (±)‐3‐(3′,4′,5′‐trimethoxyphenyl)propane‐1,2‐diol (4), (+)‐syringaresinol (5), (7S,8R,8′R)‐5,5′‐dimethoxylariciresinol (6), juniperoside (7) were isolated from the leaves of Trigonostemon honbaensis. Their chemical structures were determined using ESI‐MS, 1D NMR, and 2D NMR spectra and in comparison with the reported literature. Compounds1‐ 7 were reported from Trigonostemongen
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Vikas, Kumar, and Kumar Goyal Pramod. "Design, Synthesis, and Anticancer Activity of N-(Substituted Phenyl)-5- (3,4,5-Trimethoxyphenyl)-1,3,4-Oxadiazol-2-Amine Analogues: Exploring Novel Chemotherapeutic Agents." International Journal of Current Pharmaceutical Review and Research 16, no. 05 (2024): 95–108. https://doi.org/10.5281/zenodo.12785157.

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AbstractA Series of newer N-(substituent phenyl)-5-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazol-2-amine analogues 4a-fwas subjected to molecular properties prediction by mol soft and Molinspiration software and was synthesizedin satisfactory yields. All the compounds followed the Lipinski “rule of five “which makes them potentiallyactive agents. 3 Compound (4a, 4d & 4f) were evaluated for their anticancer activity in one dose assay andshowed moderate activity on various cell lines. The compound N-(2,4-dimethylphenyl)-5-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazol-2-amine (4d) showed ma
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Egorov, V. A., L. S. Khasanova, F. A. Gimalova та M. S. Miftakhov. "Double acylation product in the snсl<sub>4</sub>-promoted reaction of 4,5-dichlorocyclopent-4-en-1,3-dione with 1,3,5-trimethoxybenzene". Журнал органической химии 59, № 8 (2023): 1096–99. http://dx.doi.org/10.31857/s0514749223080128.

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The interaction of 4,5-dichlorocyclopent-4-en-1,3-dione with 1,3,5-trimethoxybenzene under Friedel-Crafts reaction conditions along with the expected 5-(2,4,6-trimethoxyphenyl)-4-chlorocyclopent-4-ene-1,3-dione obtained disubstituted product - 3,4-bis-(2,4,6-trimethoxyphenyl)-2-chlorocyclopent-2-en-1-one.
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Egorov, V. A., L. S. Khasanova, F. A. Gimalova, and M. S. Miftakhov. "Double Acylation Product in the SnCl4-promoted Reaction of 4,5-Dichlorocyclopent-4-en-1,3-dione with 1,3,5-Trimethoxybenzene." Russian Journal of Organic Chemistry 59, no. 8 (2023): 1449–52. http://dx.doi.org/10.1134/s1070428023080201.

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Abstract The reaction of 4,5-dichlorocyclopent-4-en-1,3-dione with 1,3,5-trimethoxybenzene under Friedel–Crafts reaction conditions gave, along with the expected 5-(2,4,6-trimethoxyphenyl)-4-chlorocyclopent-4-ene-1,3-dione, a disubstituted product―3,4-bis-(2,4,6-trimethoxyphenyl)-2-chlorocyclopent-2-en-1-one.
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Penthala, Narsimha Reddy, Jaishankar K. B. Yadlapalli, Sean Parkin, and Peter A. Crooks. "Crystal structures of (Z)-5-[2-(benzo[b]thiophen-2-yl)-1-(3,5-dimethoxyphenyl)ethenyl]-1H-tetrazole and (Z)-5-[2-(benzo[b]thiophen-3-yl)-1-(3,4,5-trimethoxyphenyl)ethenyl]-1H-tetrazole." Acta Crystallographica Section E Crystallographic Communications 72, no. 5 (2016): 652–55. http://dx.doi.org/10.1107/s2056989016005600.

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(Z)-5-[2-(Benzo[b]thiophen-2-yl)-1-(3,5-dimethoxyphenyl)ethenyl]-1H-tetrazole methanol monosolvate, C19H16N4O2S·CH3OH, (I), was prepared by the reaction of (Z)-3-(benzo[b]thiophen-2-yl)-2-(3,5-dimethoxyphenyl)acrylonitrile with tributyltin azideviaa [3 + 2]cycloaddition azide condensation reaction. The structurally related compound (Z)-5-[2-(benzo[b]thiophen-3-yl)-1-(3,4,5-trimethoxyphenyl)ethenyl]-1H-tetrazole, C20H18N4O3S, (II), was prepared by the reaction of (Z)-3-(benzo[b]thiophen-3-yl)-2-(3,4,5-trimethoxyphenyl)acrylonitrile with tributyltin azide. Crystals of (I) have two molecules in t
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Mohamed, Mosaad, Samir Awad, and Naglaa Ahmed. "Synthesis and antimicrobial evaluation of some 6-aryl-5-cyano-2-thiouracil derivatives." Acta Pharmaceutica 61, no. 2 (2011): 171–85. http://dx.doi.org/10.2478/v10007-011-0019-1.

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Synthesis and antimicrobial evaluation of some 6-aryl-5-cyano-2-thiouracil derivativesA series of 6-aryl-5-cyano-2-thiouracil derivatives (1a-d) was synthesized by the reaction of ethyl cyanoacetate with thiourea and aldehydes. These products were used as intermediate compounds for the synthesis of a number of thiouracil derivatives (2a-dto10a-d). All compounds were screened for antibacterial and antifungal activities. Some of the prepared compounds, 6-(4-fluorophenyl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxamide (2a), 4-oxo-2-thioxo-6-(3,4,5-trimethoxyphenyl)-1,2,3,4-tetrahydropy
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Saidi, Nurdin, Hiroshi Morita, Marc Litaudon, Mohd Azlan Naflah, Khalijah Awang, and Mustanir. "New Phenyl Propanoids from Cryptocarya bracteolata." Natural Product Communications 11, no. 6 (2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100629.

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Two new phenyl propanoids were extracted from the bark of Cryptocarya bracteolate Gamb., ethyl 3-(2′-hydroxy-3′,4′,5′-trimethoxyphenyl) propanoate (1) and ethyl 3-(2′-glucosyl-3′,4′,5′-trimethoxyphenyl)propanoate(2), together with seven known alkaloids, (+)-lirioferine (3), (+)-bracteoline (4), (+)-reticuline (5), (+)-reticulineN-oxide (6), (-)-norargemonine (7), (+)-bisnorargemonine (8) and atherolin (9). The structures of compounds were established through several spectroscopic methods; ID and 2D-NMR, UV, IR and MS.
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Book chapters on the topic "5- trimethoxyphenyl)-1"

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Aggarwal, P., and M. W. P. Bebbington. "Cyclization of 5-[Hydrazono(3,4,5-trimethoxyphenyl)methyl]-1,2,4-triazin-6(1)-ones." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00253.

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Conference papers on the topic "5- trimethoxyphenyl)-1"

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Prabhu, A. N., V. Upadhyaya, A. Jayarama, et al. "Synthesis, Growth And Characterization of 1-(5-chlorothiophen-2-yl)-3-(2,4,5-Trimethoxyphenyl) Prop-2-en-1-one Single Crystal: A Potential NLO Material." In OPTICS: PHENOMENA, MATERIALS, DEVICES, AND CHARACTERIZATION: OPTICS 2011: International Conference on Light. AIP, 2011. http://dx.doi.org/10.1063/1.3643603.

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