97305-94-7Relevant academic research and scientific papers
Iodine(III)-mediated umpolung of bromide salts for the ethoxybromination of enamides
Nocquet-Thibault, Sophie,Retailleau, Pascal,Cariou, Kevin,Dodd, Robert H.
supporting information, p. 1842 - 1845 (2013/06/04)
Using (diacetoxyiodo)benzene in conjunction with simple bromide salts in ethanol allows the regioselective ethoxybromination of a wide range of enamides, thus yielding highly versatile α-bromo hemiaminals, which can then be engaged in a broad array of transformations.
N-Alkylation of some Secondary Styryl Enamides
Brettle, Roger,Shibib, Sa'ad M.,Wheeler, Kevin J.
, p. 831 - 836 (2007/10/02)
The preparation of some secondary styryl enamides of both the Z-and E-configuration, and their exclusively N-alkylation through their anions is described.Partial configurational inversion is observed under certain conditions during the alkylation of the d
