Thiol-induced nitric oxide donation mechanisms in substituted dinitrobenzofuroxans
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文摘
Dinitrofuroxans with π-donor substituents in the position 7 are prone to N-oxidic tautomerism. Furoxans easier donate NO in the 3-N-oxide form than in 1-N-oxide form. 7-Substituted furoxans are not affected by the Boulton-Katritzky reaction. 7-Substituted dinitrofuroxans exist in two atropisomeric forms. NO donation is easier in anti atropisomer.
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