1007389-65-2Relevant academic research and scientific papers
Enantioselective cascade radical addition-cyclization-trapping reactions
Miyabe, Hideto,Asada, Ryuta,Toyoda, Akira,Takemoto, Yoshiji
, p. 5863 - 5866 (2006)
(Chemical Equation Presented) In addition: The chiral Lewis acid mediated radical addition-cyclization-trapping reaction of a hydroxamate ester with two radical acceptors provides a cascade approach for the asymmetric synthesis of various γ-lactams (see s
Cascade radical reaction of substrates with a carbon-carbon triple bond as a radical acceptor
Miyabe, Hideto,Asada, Ryuta,Takemoto, Yoshiji
supporting information, p. 1148 - 1155 (2013/07/26)
The limitation of hydroxamate ester as a chiral Lewis acid coordination moiety was first shown in an intermolecular reaction involving a radical addition and sequential allylation processes. Next, the effect of hydroxamate ester was studied in the cascade
Polarity-mismatched addition of electrophilic carbon radicals to an electron-deficient acceptor: Cascade radical addition-cyclization-trapping reaction
Yoshioka, Eito,Kohtani, Shigeru,Sawai, Kaori,Kentefu,Tanaka, Eri,Miyabe, Hideto
, p. 8588 - 8604,17 (2020/09/15)
The polarity-mismatched perfluoroalkyl radical addition to electron-deficient alkenes was studied. For this study, several substrates having two polarity-different radical acceptors were employed to investigate the regiochemical courses of cascade reactio
