334251

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Addressing the unusual reactivity of 2-pyridinecarboxaldehyde and 2-quinolinecarboxaldehyde in base-catalyzed aldol reactions with acetophenone.

Wachter-Jurcsak N, et al.

Tetrahedron Letters, 39(23), 3903-3906 (1998)

DNA targeting half sandwich Ru(II)-p-cymene-N^N complexes as cancer cell imaging and terminating agents: influence of regioisomers in cytotoxicity.

Ashaparna Mondal et al.

Dalton transactions (Cambridge, England : 2003), 50(3), 979-997 (2020-12-24)

For diagnosing and annihilating cancer in the human body, herein, we have adopted a one pot convenient synthetic protocol to synthesize a library of half sandwich Ru(ii)-p-cymene-N^N complexes under continuous sonication and isolated their regioisomers by preparative thin layer chromatography

A sugar-quinoline fluorescent chemosensor for selective detection of Hg2+ ion in natural water.

Shengju Ou et al.

Chemical communications (Cambridge, England), (42)(42), 4392-4394 (2006-10-24)

A selective and sensitive fluorescent sensor for detection of Hg2+ in natural water was achieved by incorporating the well-known fluorophore quinoline group and a water-soluble D-glucosamine group within one molecule.

Mixed ligand copper(II) complexes of 1,10-phenanthroline with tridentate phenolate/pyridyl/(benz)imidazolyl Schiff base ligands: covalent vs non-covalent DNA binding, DNA cleavage and cytotoxicity.

Chandrasekaran Rajarajeswari et al.

Journal of inorganic biochemistry, 140, 255-268 (2014-09-10)

A series of copper(II) complexes of the types [Cu(L)(phen)](ClO4) 1-2, where HL is a tridentate ligand with two nitrogen and one oxygen donor atoms (2NO) such as 2-(2-(1H-benzimidazol-2-yl)ethyliminomethyl)phenol (HL1) and 2-(2-(1H-benzimidazol-2-yl)ethyl-imino)methyl)-4-methylphenol (HL2), phen is 1,10-phenanthroline and [Cu(L)(phen)](ClO4)23-6, where L is

Targeting of Cellular Organelles by Fluorescent Plasmid DNA Nanoparticles.

Diana Costa et al.

Biomacromolecules, 18(9), 2928-2936 (2017-08-17)

The development of a suitable delivery system and the targeting of intracellular organelles are both essential for the success of drug and gene therapies. The conception of fluorescent ligands, displaying targeting specificity together with low toxicity, is an emerging and

Time-of-flight accurate mass spectrometry identification of quinoline alkaloids in honey.

Tamara Rodríguez-Cabo et al.

Analytical and bioanalytical chemistry, 407(20), 6159-6170 (2015-06-05)

Time-of-flight accurate mass spectrometry (TOF-MS), following a previous chromatographic (gas or liquid chromatography) separation step, is applied to the identification and structural elucidation of quinoline-like alkaloids in honey. Both electron ionization (EI) MS and positive electrospray (ESI+) MS spectra afforded

Mechanism of Evolution of Koneramine Complexes from One-Pot Reactions: Snapshots of Intermediates Offer Facile Routes to New Dipicolylamines.

Sakthi Raje et al.

Chemistry, an Asian journal, 13(11), 1458-1466 (2018-04-01)

Koneramines (LR OR', R=Ph or Ts; R'=Me, iPr) and their complexes were found to emerge from the system of pyridine-2-carboxaldehyde and N-phenyl/tosylethylenediamine when a primary or secondary alcohol was used as solvent. Imidazolidinylpyridines (LR , R=Ph or Ts) became major

Copper (I)-imine complexes: Synthesis and catalytic activity in olefin cyclopropanation

Attilio Ardizzoia G, et al.

Inorgorganica Chimica Acta, 362(10), 3507-3512 (2009)

Organometallic Conjugates of the Drug Sulfadoxine for Combatting Antimicrobial Resistance.

Prinessa Chellan et al.

Chemistry (Weinheim an der Bergstrasse, Germany) (2018-04-14)

Fourteen novel arene RuII , and cyclopentadienyl (Cpx ) RhIII and IrIII complexes containing an N,N'-chelated pyridylimino- or quinolylimino ligand functionalized with the antimalarial drug sulfadoxine have been synthesized and characterized, including three by X-ray crystallography. The rhodium and iridium

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