0000000000185517

AUTHOR

J. Barbe

showing 2 related works from this author

Analysis of pyridoquinoline derivatives by liquid chromatography/atmospheric pressure chemical ionization mass spectrometry

2001

A method using liquid chromatography/atmospheric pressure chemical ionization mass spectrometry (LC/APCI-MS) has been developed for the characterization and determination of pyridoquinoline derivatives 4,6-bis(dimethylaminoethylamino)-2,8,10-trimethylpyrido[3,2-g]quinoline, 4,6-bis(dimethylaminoethoxy)-2,8,10-trimethylpyrido[3,2-g]quinoline and 4,6-bis[(dimethylaminoethyl)thio]-2,8,10-trimethylpyrido[3,2-g] quinoline, all with potential antitumor properties. LC separation was performed on a conventional C18 column using a binary mobile phase composed of acetonitrile and 50 mM aqueous ammonium formate at pH 3. The APCI mass spectra obtained showed that proton addition giving [M + H]+ was the…

ChromatographyAqueous solutionOrganic ChemistryQuinolineAnalytical chemistryAtmospheric-pressure chemical ionizationMass spectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryIonizationAmmonium formateMass spectrumAcetonitrileSpectroscopyRapid Communications in Mass Spectrometry
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Improved routes for the synthesis of face-to-face bismacrocycles in porphyrin and corrole series

2005

Face-to-face bismacrocycles involving porphyrinoid species are still of great interest owing to their versatile properties. Despite the fact that their syntheses generally involve several steps, numerous modifications have been made in their synthetic pathways thus allowing their preparation in gram quantities. Here we report on recent improvements we could propose especially for the synthesis of bisporphyrin, biscorrole and porphyrin-corrole derivatives.

chemistry.chemical_compoundChemistryOrganic chemistryGeneral ChemistryGeneral MedicineCorroleCombinatorial chemistryPorphyrin
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