Reaction of nitric oxide with benzyl cyanide to yield a bis-diazeniumdiolated imidate

Author:

Arnold Ernst V,Keefer Larry K,Hrabie Joseph A

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. Keefer, L. K. CHEMTECH 1998, 28 (No. 8), 30–35.

2. Keefer, L. K.; Christodoulou, D.; Dunams, T. M.; Hrabie, J. A.; Maragos, C. M.; Saavedra, J. E.; Wink, D. A. In Nitrosamines and Related N-Nitroso Compounds: Chemistry and Biochemistry; Loeppky, R. N.; Michejda, C. J., Eds. Chemistry of the ‘NONOates’, unusual N-nitroso compounds formed by reacting nitric oxide with nucleophiles. American Chemical Society: Washington, 1994; pp. 136−146.

3. Hrabie, J. A.; Keefer, L. K. In Pathophysiology and Clinical Applications of Nitric Oxide Part B; Rubanyi, G. M., Ed. Nitric oxide donors. Harwood Academic Publishers: Richmond, CA, 1999; pp. 455–470.

4. “NONOates” (1-substituted diazen-1-ium-1,2-diolates) as nitric oxide donors: Convenient nitric oxide dosage forms

5. Maskill, H.; Menneer, I. D.; Smith, D. I. J. Chem. Soc., Chem. Commun. 1995, 1855–1856.

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