53388-83-3Relevant academic research and scientific papers
Decarboxylative acylation of indolines with α-keto acids under palladium catalysis: A facile strategy for the synthesis of 7-substituted indoles
Kim, Minyoung,Kumar Mishra, Neeraj,Park, Jihye,Han, Sangil,Shin, Youngmi,Sharma, Satyasheel,Lee, Youngil,Lee, Eui-Kyung,Kwak, Jong Hwan,Kim, In Su
supporting information, p. 14249 - 14252 (2014/12/11)
Palladium-catalyzed decarboxylative acylation of highly substituted indolines with α-keto acids via C-H bond activation is described. This protocol provides efficient access to C7-carbonylated indoles known to have diverse biological profiles. This journal is
The Chemistry of Pentavalent Organobismuth Reagents. Part 7. The Possible Role of Radical Mechanisms in the Phenylation Process for Bismuth(V), and Related Lead(IV), Iodine(III), and Antimony(V) Reagents
Barton, Derek H. R.,Finet, Jean-Pierre,Giannotti, Charles,Halley, Frank
, p. 241 - 250 (2007/10/02)
The phenylation reactions of bismuth(V), lead(IV), and iodine(III) have been examined to test the presence or absence of phenyl radicals.In the case of several bismuth(V) reactions the presence of phenyl radicals has been detected, but it has been shown, by use of a large excess of radical trapping agent, that these radicals have nothing to do with the phenylation process.In the same way, the other phenylation reactions fail to respond to a large excess of a radical trap.
