High impact information on NSC73907

• Two azo-ene-butadiyne conjugated systems undergo CuCl-mediated cyclization to afford isoindazolyl carbenoids that could be trapped with 2,3-dimethyl-2-butene as [2 + 1] cycloaddition products [1].
• We have developed a technique based on solid-phase microextraction (SPME) and gas chromatography/mass spectrometry (GC/MS) to quantify the acids, as well as other products, and applied it to the reactions of ozone with propene, trans-2-butene, 2,3-dimethyl-2-butene, and isoprene [2].
• Kinetics and mechanism of photocycloaddition of deoxyuridines to 2,3-dimethyl-2-butene [3].
• Singlet oxygen generation, monitored using the singlet oxygen trap tetramethylethylene, and oxygen consumption in isolated mitochondria sensitized by hypericin were also light-dose and wavelength dependent [4].
• For example, 1,1-dichloro-2,2,3,3-tetramethylcyclopropane was identified as a metabolite by gas chromatography mass spectrometry when carbon tetrachloride (CCl4) was incubated anaerobically with rat liver microsomes, NADPH and 2,3-dimethyl-2-butene [5].

Associations of NSC73907 with other chemical compounds

• The plots of log kq versus the ionization potential for cyclohexene, 2-methylbut-1-ene, 2-methylbut-2-ene, 2,3-dimethylbut-2-ene, trans-penta-1,3-diene, ethyl vinyl ether and ethyl prop-1-en-1-yl ether are linear with a slope of -2.7/eV (r = 0.98) for 1 and -2.6/eV (r = 0.95) for 2 [6].

Gene context of NSC73907

• The kinetics of formation of the ESR signal corresponding to the photoreduction of the nitrodiphenyl ether in the presence of TME behave differently in a micellar environment as compared to solution [7].

References