Chemistry of the Diazeniumdiolates: <i>Z</i> ⇌ <i>E</i> Isomerism
Yan-Ni Wang(Frederick National Laboratory for Cancer Research), Joseph Ivanic(Leidos (United States)), Jack Collins(National Institutes of Health), Jeffrey R. Deschamps(United States Naval Research Laboratory), Challice L. Bonifant(Johns Hopkins University), David J. Waterhouse, Larry K. Keefer(Unknown), Joseph E. Saavedra(Genesis Laboratories), J.L. Flippen-Anderson(Frederick National Laboratory for Cancer Research), Gwendolyn N. Chmurny(Frederick National Laboratory for Cancer Research), D. Scott Bohle(University of Chicago), Keith M. Davies(George Mason University), John R. Klose(Frederick National Laboratory for Cancer Research)
Cited by 15
Related Papers
“NONOates” (1-substituted diazen-1-ium-1,2-diolates) as nitric oxide donors: Convenient nitric oxide dosage forms
|Methods in enzymology on CD-ROM/Methods in enzymology|1996|674
Cu-catalyzed cross-dehydrogenative coupling: A versatile strategy for C–C bond formations via the oxidative activation of sp <sup>3</sup> C–H bonds
|Proceedings of the National Academy of Sciences|2006|592
Nitric Oxide-Releasing Polymers Containing the [N(O)NO]<sup>-</sup>Group
|Journal of Medicinal Chemistry|1996|207
Chemistry of the Diazeniumdiolates. 2. Kinetics and Mechanism of Dissociation to Nitric Oxide in Aqueous Solution
|Journal of the American Chemical Society|2001|206
Targeted multicolor in vivo imaging over 1,000 nm enabled by nonamethine cyanines
|Nature Methods|2022|178