@article{oai:muroran-it.repo.nii.ac.jp:00009477,
 author = {CHENNAPURAM, Madhu and チェンアプラム, マデュー and Subba Reddy, Ummareddy Venkata 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 = {12},
 journal = {European Journal of Organic Chemistry},
 month = {Mar},
 note = {application/pdf, A series of new hybrid type squaramide-fused amino alcohol (SFAA) catalysts were synthesized and their catalytic efficiency in enantioselective nitro-aldol reaction of various isatins with nitromethane that afford the chiral 3-substituted 3-hydroxyoxindoles in excellent chemical yields (up to 99%) and high enantioselectivities (up to 95% ee) is described. The resulting chiral 3-hydroxyoxindoles could be used as synthetic precursors for the synthesis of several natural products with a broad spectrum of fascinating biological activities.},
 pages = {1638--1646},
 title = {Hybrid-Type Squaramide-Fused Amino Alcohol Organocatalysts for Enantioselective Nitro-Aldol Reaction of Nitromethane with Isatins},
 year = {2017},
 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}
}