1190307-41-5Relevant academic research and scientific papers
Enantioselective Diels-Alder reaction of 1,2-dihydropyridines with aldehydes using β-amino alcohol organocatalyst
Kohari, Yoshihito,Okuyama, Yuko,Kwon, Eunsang,Furuyama, Taniyuki,Kobayashi, Nagao,Otuki, Teppei,Kumagai, Jun,Seki, Chigusa,Uwai, Koji,Dai, Gang,Iwasa, Tatsuo,Nakano, Hiroto
, p. 9500 - 9511 (2015/01/09)
(Chemical Equation Presented) The enantioselective Diels-Alder reaction of 1,2-dihydropyridines with aldehydes using an easily prepared optically active β-amino alcohol catalyst was found to provide optically active isoquinuclidines, an efficient syntheti
Asymmetric total synthesis of (+)-luciduline: Toward a general approach to related lycopodium alkaloids
Barbe, Guillaume,Fiset, Dominic,Charette, Andre B.
, p. 5354 - 5362 (2011/08/06)
As part of a research program directed toward the synthesis of Lycopodium alkaloids, a multigram scale asymmetric synthesis of intermediate 11 was achieved in 11 steps from pyridine (17). In addition to our alkene metathesis strategy, a key feature of thi
A novel chiral oxazolidine organocatalyst for the synthesis of an oseltamivir intermediate using a highly enantioselective Diels-Alder reaction of 1,2-dihydropyridine
Nakano, Hiroto,Osone, Kenichi,Takeshita, Mitsuhiro,Kwon, Eunsang,Seki, Chigusa,Matsuyama, Haruo,Takano, Nobuhiro,Kohari, Yoshihito
scheme or table, p. 4827 - 4829 (2010/09/16)
Enantioselective Diels-Alder reactions of 1,2-dihydropyridines with acroleins using a novel chiral oxazolidine organocatalyst afforded chiral isoquinuclidines that is an efficient synthetic intermediate of oseltamivir, with fairly good chemical yield and
