78707-65-0Relevant academic research and scientific papers
Electrocatalytic generation of amidyl radicals for olefin hydroamidation: Use of solvent effects to enable anilide oxidation
Zhu, Lin,Xiong, Peng,Mao, Zhong-Yi,Wang, Yong-Heng,Yan, Xiaomei,Lu, Xin,Xu, Hai-Chao
, p. 2226 - 2229 (2016/02/19)
Oxidative generation of synthetically important amidyl radicals from N-H amides is an appealing and yet challenging task. Previous methods require a stoichiometric amount of a strong oxidant and/or a costly noble-metal catalyst. We report herein the first electrocatalytic method that employs ferrocene (Fc), a cheap organometallic reagent, as the redox catalyst to produce amidyl radicals from N-aryl amides. Based on this radical-generating method, an efficient intramolecular olefin hydroamidation reaction has been developed. Easy access to N-arylamidyl radicals: The first electrocatalytic method for the generation of amidyl radicals from anilides has been developed using ferrocene (Cp2Fe) as a highly reactive, yet chemoselective redox catalyst. Based on this radical-generating method, a highly chemo- and diastereoselective olefin hydroamidation reaction has been developed.
ACID CATALYZED COPE REARRANGEMENTS OF 2-ACYL-1,5-DIENES
Dauben, William G.,Chollet, Andre
, p. 1583 - 1586 (2007/10/02)
The Cope rearrangement of 1,5-dienes bearing acyl substitutents in the 2-position of the diene system is strongly accelerated by protic and Lewis acids.
A Total Synthesis of (+/-)-Eremophilenolide
Pennanen, Seppo
, p. 261 - 264 (2007/10/02)
(+/-)-Eremophilenolide was synthesized in 18percent overall yield from cyclohexanone.The A/B-ring system was prepared via butenylcyclohexenol-annulation and the 2-furanone unit via α-epoxyketone-ynamine reaction.
