113933-16-7Relevant academic research and scientific papers
Methods for treating neisseria gonorrhoeae infection with substituted 1,2-dihydro-2A,5,8A-triazaacenaphthylene-3,8-diones
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, (2020/07/21)
The present invention relates to methods for treating Neisseria Gonorrhoeae infection which comprises administering to a subject in need thereof novel 1,2-dihydro-2a,5,8a-triazaacenaphthylene-3,8-dione compounds: or pharmaceutically acceptable salts thereof and/or corresponding pharmaceutical compositions.
TRICYCLIC NITROGEN CONTAINING COMPOUNDS AS ANTIBACTERIAL AGENTS
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, (2008/12/08)
Tricyclic nitrogen containing compounds and their use as antibacterials. Z1and Z2 are independently selected from CH and N.
Substituted DTPA monoamides of the central carboxylic acid group and their metal complexes
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, (2008/06/13)
Diethylenetriaminepentaacetic acid monoamide derivatives, their complexes and complex salts, containing an element of atomic numbers 21-29, 31, 32, 39, 42-44, 49 or 57-83, pharmaceutical agents containing these compounds, their use as contrast media and process for their production.
Process for the production of DTPA-monoamides of the central carboxylic acid and their use as pharmaceutical agents
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, (2008/06/13)
A process for the production of of general formula I diethylenetriaminepentacarboxylic acid monoamide derivatives STR1 in which E1, E2 and Z have varying meanings.
Process for the production of DTPA-tetraesters of terminal carboxylic acids
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, (2008/06/13)
The invention relates to a process for the production of diethylenetriaminepentacarboxylic acid tetraesters of general formula I STR1 in which R1 and Z have different meanings.
One-pot alkoxymercuriation-bromodemercuriation: A versatile access to 3-alkoxy-2-bromopropanoic esters
Anelli,Beltrami,Lolli,Uggeri
, p. 2639 - 2645 (2007/10/02)
A convenient one-pot methodology for the preparation of 3-alkoxy-2-bromopropanoic esters from alkyl acrylates is described. The use of stoichiometric amounts of alkyl acrylate, alcohol and mercury trifluoroacetate in THF makes this procedure versatile and attractive to achieve building blocks for the synthesis of targeted contrast agents for Magnetic Resonance Imaging.
