Nitrogen-bound diazeniumdiolated amidines

In contrast to amidines bearing ionizable alpha-CH bonds, which react with nitric oxide (NO) to add diazeniumdiolate groups at their alpha-carbons, benzamidine forms an N-bound diazeniumdiolate that can be further derivatized at the other amidine nitrogen and/or the terminal oxygen to form caged NO...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2010-08, Vol.46 (31), p.5799-5801
Hauptverfasser: Biswas, Debanjan, Deschamps, Jeffrey R, Keefer, Larry K, Hrabie, Joseph A
Format: Artikel
Sprache:eng
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Zusammenfassung:In contrast to amidines bearing ionizable alpha-CH bonds, which react with nitric oxide (NO) to add diazeniumdiolate groups at their alpha-carbons, benzamidine forms an N-bound diazeniumdiolate that can be further derivatized at the other amidine nitrogen and/or the terminal oxygen to form caged NO compounds as potential NO prodrugs.
ISSN:1359-7345
1364-548X
1364-548X
DOI:10.1039/c0cc00849d