• Design and synthesis of coumarin based sensitizers for dyesensitized solar cells dsscs synthesis of novel colorants for dyesensitized solar cells and use of greener protocols for heterocyclic synthesis page 41 owing to the possibility of isomer formation. (web.app)
  • Some cell wall polysaccharide synthesis and cytoskeleton formation-related proteins were up-regulated by JA to promote tuber cell expansion. (biomedcentral.com)
  • The present work involves the design and synthesis of some novel acyl hydrazone based molecular hybrids of 1,4-dihydropyridine and pyrazole ( 5a - g ). (biomedcentral.com)
  • Acetone hydrazone (isopropylidenehydrazine) is the product of condensation of acetone and hydrazine, as typical for hydrazone formation. (wikipedia.org)
  • Acetone hydrazone can be produced on large scale by reaction of acetone azine with hydrazine, a more convenient reaction that direct reaction of acetone and hydrazine. (wikipedia.org)
  • Likewise, it is susceptible to disproportionation to revert to acetone azine and hydrazine, especially in the presence of water. (wikipedia.org)
  • ChromaLINK bioconjugation technology is based on the formation of a stable bis-arylhydrazone formed from an aromatic hydrazine and an aromatic aldehyde. (vectorlabs.com)
  • S-HyNic (succinimidyl 6-hydrazinonicotinate acetone hydrazone, SANH) is used to incorporate aromatic hydrazine moieties on biomolecules. (vectorlabs.com)
  • Phenylketene formation competes with cyclization of the. (web.app)
  • It has been shown by 1 H and 13 C NMR spectroscopy that 2-mercaptobenzoyl- hydrazones of aliphatic and aromatic aldehydes exist in solution as tautomeric mixtures of linear and cyclic benzo-1,3,4-thiadiazepine forms. (scirp.org)
  • For common ketones, some traditional names such as acetone and benzophenone predominate, and these are considered retained IUPAC names [2] , although some introductory chemistry texts use names such as propanone. (wikidoc.org)
  • Therefore here in this study, we have decided to construct the molecular hybrids based on 1,4-DHP and pyrazole moieties using acyl hydrazone linkage which may possibly circumvent the antiplasmodial drug resistance (Fig. 1 ). (biomedcentral.com)
  • With the 18 kinds of solid-liquid equilibrium diagrams thereby obtained, relationship between the ability for molecular compound formation and structure of the components was examined. (go.jp)
  • Both of the reagents result in the formation of the same end product, irrespective of the reagents used. (vedantu.com)
  • Potato tuber development is important for the formation of tuber yield and quality traits. (biomedcentral.com)
  • Acyl hydrazones are an important class of heterocyclic compounds promising pharmacological characteristics. (biomedcentral.com)
  • The linear hydrazone form is represented by (E,E')- and (E,Z')-conformational isomers, differing in the disposition relative to the amide C?N bond. (scirp.org)
  • Addition of a HyNic-modified biomolecule to a 4FB-modified biomolecule or surface directly leads to the formation of the conjugate (Figure 1). (vectorlabs.com)
  • Cell viability, colony formation, and wound healing assays were performed to determine proliferative and migratory characteristics. (fabad.org.tr)
  • 3- Cyano pyridone derivatives were synthesized by treating 1-(4-bromophenyl)-3-(4-(dimethyl amino) phenyl) prop-2-en-1-one with compounds containing active methylene group in the presence of ammonium acetate. (tsijournals.com)
  • The orientation and relative strength of participation of neighboring groups during the formation of azoline ring by treatment of N-thiobenzoyl, N-benzoyl, and N-benzimidoyl derivatives of dl -2-aminocyclohexanols and dl -2-aminohexanethiols with phosphorus pentoxide or thionyl chloride were comparatively examined with the reaction products obtained (Table I and II). (go.jp)
  • The epimeric dl -1-phenyl-2-aminopropanethiols ( threo -XI and erythro -XI), corresponding to thiol derivatives of norephedrine, were synthesized by various routes and their configurations were assigned from their formation mechanism and chemical properties. (go.jp)
  • The addition of a tetrabutylammonium halide salt additive as much as doubles the rate of formation of the intermediate acyl fluoride, yet there is no effect on the rate of consumption of this intermediate by the nucleophilic coupling partner. (ubc.ca)
  • Likewise, it is susceptible to disproportionation to revert to acetone azine and hydrazine, especially in the presence of water. (wikipedia.org)