1284303-78-1Relevant articles and documents
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
A highly enantioselective Diels-Alder reaction of 1,2-dihydropyridine using a simple β-amino alcohol organocatalyst for a practical synthetic methodology of oseltamivir intermediate
Suttibut, Chonticha,Kohari, Yoshihito,Igarashi, Ko,Nakano, Hiroto,Hirama, Masafumi,Seki, Chigusa,Matsuyama, Haruo,Uwai, Koji,Takano, Nobuhiro,Okuyama, Yuko,Osone, Kenichi,Takeshita, Mitsuhiro,Kwon, Eunsang
supporting information; experimental part, p. 4745 - 4748 (2011/10/02)
An easily prepared chiral amino alcohol catalyst was found to provide an efficient synthetic intermediate of oseltamivir with excellent chemical yield and enantioselectivity (up to 98% yield and up to 98% ee) in enantioselective Diels-Alder reactions of 1