@article{d65976e8f09f4eed9a68efe1a56c2eb2,
title = "Amino amide organocatalysts for asymmetric michael addition of β-Keto esters with β-nitroolefins",
abstract = "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).",
keywords = "Amino amide, Michael addition, Organocatalyst",
author = "Owolabi, {Isiaka Alade} and Madhu Chennapuram and Chigusa Seki and Yuko Okuyama and Eunsang Kwon and Koji Uwai and Michio Tokiwa and Mitsuhiro Takeshita and Hiroto Nakano",
note = "Funding Information: We thank Adaptable & Seamless Technology Transfer Program through Target-driven R&D from Japan Science and Technology Agency (JST) and Muroran Institute of Technology for partial financial support of this study. Publisher Copyright: {\textcopyright} 2019 The Chemical Society of Japan",
year = "2019",
doi = "10.1246/bcsj.20180302",
language = "English",
volume = "92",
pages = "696--701",
journal = "Bulletin of the Chemical Society of Japan",
issn = "0009-2673",
publisher = "The Chemical Society of Japan",
number = "3",
}