1286261-75-3Relevant academic research and scientific papers
Decarbonylative cross coupling of phthalimides with diorganozinc reagents - Efforts toward catalysis
Deglopper, Kimberly S.,Fodor, Sarah K.,Endean, Thomas B.D.,Johnson, Jeffrey B.
, p. 393 - 398 (2016)
The decarbonylative coupling of phthalimides with diorganozinc reagents to form o-substituted benzamides has been previously demonstrated as a viable process, but only with stoichiometric nickel(0). Investigations into a number of reaction variables, incl
Nickel-mediated decarbonylative cross-coupling of phthalimides with in situ generated diorganozinc reagents
Havlik, Sarah E.,Simmons, Jessica M.,Winton, Valerie J.,Johnson, Jeffrey B.
experimental part, p. 3588 - 3593 (2011/06/26)
The nickel-mediated cross-coupling of phthalimides with diorganozinc reagents proceeds via a decarbonylative process to produce ortho-substituted benzamides in high yields. In addition to tolerating diverse phthalimide functionality, including alkyl, aryl
