Articles with "synthesis derivatives" as a keyword



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Polyphthalaldehyde: Synthesis, Derivatives, and Applications.

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Published in 2018 at "Macromolecular rapid communications"

DOI: 10.1002/marc.201700519

Abstract: o-Phthalaldehyde is, to this day, the only aromatic aldehyde that can be homopolymerized through chain-growth polymerization. The product, polyphthalaldehyde (PPA), is a brittle white solid, and, having a polyacetal main chain, presents the ability to… read more here.

Keywords: ppa; polyphthalaldehyde synthesis; chemistry; synthesis derivatives ... See more keywords
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Synthesis of Derivatives of the 2-Arylquinoline Alkaloid Dubamine and their Cytotoxicity

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Published in 2020 at "Chemistry of Natural Compounds"

DOI: 10.1007/s10600-020-03074-3

Abstract: 5′-Nitro- ( 2 ) and 5′-aminodubamine ( 3 ) were sequentially synthesized from the alkaloid dubamine. Condensation of 3 with 15 aldehydes gave imines, reduction of which produced secondary amines. Studies of the cytotoxicities for… read more here.

Keywords: alkaloid dubamine; dubamine cytotoxicity; arylquinoline alkaloid; dubamine ... See more keywords
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Imogolite: a nanotubular aluminosilicate: synthesis, derivatives, analogues, and general and biological applications

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Published in 2021 at "Materials Chemistry Frontiers"

DOI: 10.1039/d1qm00617g

Abstract: Imogolite is an aluminosilicate of empirical formula (OH)3Al2O3–SiOH and hollow nanotube structure. It can be obtained from natural volcanic ash or via chemical synthesis. The inner and outer surfaces can be modified by various strategies. read more here.

Keywords: derivatives analogues; aluminosilicate synthesis; imogolite nanotubular; synthesis derivatives ... See more keywords

Synthesis of the Derivatives of 4-(5-Aryl-3-methylfuran-3-yl)-1,2,3-thiadiazole and Functionalization of 5-Aryl-2- methylfuran via Reactions of Thiadiazole Ring

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Published in 2018 at "Russian Journal of General Chemistry"

DOI: 10.1134/s1070363218070095

Abstract: By arylation of 2-methyl-3-acetylfuran via the Gomberg–Bachmann reaction 5-(4-ethoxycarbonylphenyl)-, 5-(2-nitrophenyl), and 5-(4-nitrophenyl)-2-methyl-3-acetylfurans were synthesized. Carboethoxyhydrazones of 2-methyl-5-phenyl-3-acetylfuran and its phenyl-substituted analogs when treated with thionyl chloride form 4-(5-aryl-2-methylfuran-3-yl)-1,2,3-thiadiazoles by the Hurd–Mori reaction. Thermal stability of… read more here.

Keywords: methylfuran thiadiazole; derivatives aryl; synthesis derivatives; aryl ... See more keywords