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http://dx.doi.org/10.2967/jnumed.119.241075 | DOI Listing |
J Nucl Med
November 2020
Yale University School of Medicine 801 Howard Ave., P.O. Box 208048 New Haven, CT E-mail:
J Nucl Med
November 2020
Hôpital du Haut-Lévèque avenue de Magellan 33604 Pessac, France E-mail:
J Am Chem Soc
January 2009
Dipartimento di Scienze Chimiche ed Ambientali, Universita degli Studi dell'Insubria, Via Valleggio 11, 22100, Como, Italy.
The thermal reaction between nitrosoarenes and alkynes produces N-hydroxyindoles as the major products. The mechanism of these novel reactions has been probed using a combination of experimental and computational methods. The reaction of nitrosobenzene (NB) with an excess of phenyl acetylene (PA) is determined to be first order in each reactant in benzene at 75 degrees C.
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