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Relevant bibliographies by topics / Ω-bis(organic esters)

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Journal articles

Academic literature on the topic 'Ω-bis(organic esters)'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Ω-bis(organic esters)"

1

Canonne, P., M. Belley, G. Fytas та J. Plamondon. "Synthèses des alkyl-1 cyclanols fonctionnalisés aux positions α, β et γ de la chaîne hydrocarbonée". Canadian Journal of Chemistry 66, № 1 (1988): 168–73. http://dx.doi.org/10.1139/v88-026.

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We have developed a general and versatile synthesis of N,N-dialkylaminoalkyl-, 1-chloroalkyl-, 1-phenoxyalkyl-, 1-thiophenoxyalkyl-, 1-diethyoxyalkyl-, and 1-(1,3-dithiolane)alkylcyclanols in good yields by the reaction of α,ω-bis(bromomagnesio)alkanes with the corresponding functionalized carboxylic acid esters.

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2

Hanessian, Stephen, Hubli Prabhanjan, Dongxu Qiu, and Sudhir Nambiar. "Synthesis of chemically and functionally diverse scaffolds from pentaerythritol." Canadian Journal of Chemistry 74, no. 9 (1996): 1731–37. http://dx.doi.org/10.1139/v96-191.

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Pentaerythritol (2,2-bis-hydroxymethyl-propane-1,3-diol) was converted into a series of mono-, di-, and trisubstituted derivatives, comprising allyl ethers and amino-alkyl ethers, by systematic chemical manipulation of the hydroxy groups. The remaining hydroxymethyl group in the case of the trisubstituted analog was functionalized with ether groups bearing terminal ω-carboxyl or ω-alkene groups. These derivatives are versatile templates and scaffolds for single, double, or triple substitution with appropriate ligands forming amides and esters, and allowing the attachment of the ω-alkene or ω-c

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3

Nasser, S. A. M. Khalil, та M. Mohamed Noha. "Antimicrobial Evaluation and Structure-Activity Relationship (SAR) of Some 1,ω-bis[4-Carboxy/Methoxycarbonyl/(Hydrazinecarbonyl) /Phenoxy]Alkanes". Annual Research & Review in Biology 13, № 4 (2017): 1–10. https://doi.org/10.9734/ARRB/2017/33990.

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A series of some 1,ω-bis[4-carboxy/methoxycarbonyl/(hydrazinecarbonyl)/phenoxy]alkanes were synthesized and evaluated for their antimicrobial activity against different strains of Gram-positive bacteria (<em>Bacillus subtilis </em>RCMB 101-001 and<em> Staphylococcus aureus </em>RCMB 106-001 (1)), Gram-negative bacteria (<em>Pseudomonas aeruginosa </em>RCMB 102-002 and <em>Escherichia coli</em> RCMB 103-001), yeast (<em>Candida albicans </em>RCMB 005003) and fungi (<em>Aspergillus fumigates </em>RCMB 002008 (1), <em>Penicillium italicum</em> RCMB 001018 (1) and <em>Syncephalastrum racemosum</em

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4

Kartvelishvili, Tamara, George Tsitlanadze, Lamara Edilashvili, Nona Japaridze та Ramaz Katsarava. "Amino acid based bioanalogous polymers. Novel regular poly(ester urethane)s and poly(ester urea)s based on bis(L-phenylalanine) α,ω-alkylene diesters". Macromolecular Chemistry and Physics 198, № 6 (1997): 1921–32. http://dx.doi.org/10.1002/macp.1997.021980620.

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5

Arabuli, Natia, George Tsitlanadze, Lamara Edilashvili та ін. "Heterochain polymers based on natural amino acids. Synthesis and enzymatic hydrolysis of regular poly(ester amide)s based on bis(L-phenylalanine) α,ω-alkylene diesters and adipic acid". Macromolecular Chemistry and Physics 195, № 6 (1994): 2279–89. http://dx.doi.org/10.1002/macp.1994.021950633.

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6

Liang, Yaqin, Hui Li, Jiahui Ji, Jiayu Wang, and Yujie Ji. "Self-Aggregation, Antimicrobial Activity and Cytotoxicity of Ester-Bonded Gemini Quaternary Ammonium Salts: The Role of the Spacer." Molecules 28, no. 14 (2023): 5469. http://dx.doi.org/10.3390/molecules28145469.

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Five ester-bonded gemini quaternary ammonium surfactants C12-En-C12 (n = 2, 4, 6), with a flexible spacer group, and C12-Bm-C12 (m = 1, 2), with rigid benzene spacers, were synthesized via a two-step reaction and analyzed. Furthermore, the effects of the spacer structure, spacer length and polymerization degree on the self-aggregation, antimicrobial activity and cytotoxicity of C12-En-C12 and C12-Bm-C12 and their corresponding monomer N-dodecyl-N,N,N-trimethyl ammonium chloride DTAC were investigated. The results showed that C12-En-C12 and C12-Bm-C12 had markedly lower critical micellar concen

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