Results 21 to 30 of about 750,316 (378)
Crystal structure of 2-(4-chlorobenzamido)benzoic acid
Acta Crystallographica Section E: Crystallographic Communications, 2015 In the title molecule, C14H10ClNO3, the amide C=O bond is anti to the o-carboxy substituent in the adjacent benzene ring, a conformation that facilitates the formation of an intramolecular amide-N—H...O(carbonyl) hydrogen bond that closes an S(6) loop ...
Rodolfo Moreno-Fuquen +2 more
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Intermolecular interactions in N-(ferrocenylmethyl)anthracene-9-carboxamide [PDF]
, 2003 The title compound, [Fe(C₅H₅)(C₂₁H₁₆NO)], was synthesized from the coupling reaction of anthracene-9-carboxylic acid and ferrocenylmethylamine. The ferrocenyl (Fc) group and the anthracene ring system both lie approximately orthogonal to the amide moiety.
Gallagher, John F. +3 more
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Synthesis of Gibberellic Acid Derivatives and Their Effects on Plant Growth
Molecules, 2017 A series of novel C-3-OH substituted gibberellin derivatives bearing an amide group were designed and synthesized from the natural product gibberellic acid (GA3).
Hao Tian +6 more
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The effect of the amido substituent on polymer molecular weight in propene homopolymerisation by titanium cyclopentadienyl-amide catalysts [PDF]
, 2000 In the homopolymerisation of propene by the cyclopentadienyl-amide titanium catalyst systems [η5,η1-C5H4(CH2)2NR]TiCl2/MAO and [η5,η1-C5H4(CH2)2NR]Ti(CH2Ph)2/B(C6F5)3 (R = tBu, iPr, Me), the catalyst with the smallest substituent (Me) on the amido moiety
Hessen, Bart, +2 more
core +1 more source
Self-Assembled Fluorinated Organogelators for Surface Modification
Applied Sciences, 2012 A new class of alkyl- and perfluoroalkyl-containing urea and amide derivatives was synthesized from amino acid derivatives. Most of these compounds showed excellent gelation behavior in organic solvents at low concentrations.
Anilkumar Raghavanpillai +1 more
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Molbank, 2022 The development of new techniques for the preparation of organic compounds is important, with catalytic processes being key to this innovation. The development of copper-based metal-organic frameworks to promote oxidative couplings has allowed the ...
María Albert-Soriano, Isidro M. Pastor
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Gold amides as anticancer drugs: synthesis and activity studies [PDF]
, 2013 Modular gold amide chemotherapeutics: Access to modern chemotherapeutics with robust and flexible synthetic routes that are amenable to extensive customisation is a key requirement in drug synthesis and discovery.
Amagai +34 more
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Cinnamic Acid Conjugates in the Rescuing and Repurposing of Classical Antimalarial Drugs
Molecules, 2019 Cinnamic acids are compounds of natural origin that can be found in many different parts of a wide panoply of plants, where they play the most diverse biological roles, often in a conjugated form. For a long time, this has been driving Medicinal Chemists
Ana Teresa Silva +10 more
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Beilstein Journal of Organic Chemistry, 2017 It has been found that 2,7-di-tert-butylpyrene reacts with aliphatic iso(thio)cyanates in the presence of trifluoromethanesulfonic acid to exclusively afford the corresponding 1-substituted (thio)amides in high yields.
Anna Wrona-Piotrowicz +3 more
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Pharmaceuticals, 2021 The pharmacological inhibition of soluble epoxide hydrolase (sEH) has been suggested as a potential therapy for the treatment of pain and inflammatory diseases through the stabilization of endogenous epoxyeicosatrienoic acids.
Juan Martín-López +8 more
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