@article{oai:muroran-it.repo.nii.ac.jp:00009947,
 author = {OWOLABI, Isiaka Alade and オウォラビ, イシアカ アラデ and CHENNAPURAM, Madhu and チェンアプラム, マデュー and SEKI,  Chigusa and 関, 千草 and OKUYAMA, Yuko and 奥山, 祐子 and KWON, Eunsang and 權, 垠相 and UWAI,  Koji and 上井, 幸司 and TOKIWA, Michio and 常盤, 峻士 and TAKESHITA, Mitsuhiro and 竹下, 光弘 and 中野, 博人 and NAKANO, Hiroto},
 issue = {3},
 journal = {Bulletin of the Chemical Society of Japan},
 month = {},
 note = {application/pdf, Asymmetric Michael addition of β-keto esters with trans-β-nitroolefins using chiral amino amide organocatalyst was tried and afforded synthetically useful chiral Michael adducts in both excellent chemical yields (up to 99%) and stereoselectivities (up to dr. 99:1, up to 98% ee).},
 pages = {696--701},
 title = {Amino Amide Organocatalysts for Asymmetric Michael Addition of β-Keto Esters with β-Nitroolefins},
 volume = {92},
 year = {2019},
 yomi = {セキ, チグサ and オクヤマ, ユウコ and ウワイ, コウジ and トキワ, ミチオ and タケシタ, ミツヒロ and ナカノ, ヒロト}
}