@article{e3d1c66c2cf244e99f6fded15efc1954,
title = "2-Azanorbornane-Based Amino Alcohol Organocatalysts for Asymmetric Michael Reaction of β-Keto Esters with Nitroolefins",
abstract = "New optically active 2-azanorbornane-based amino alcohol organocatalysts were designed and synthesized, and these catalysts were successfully employed in the asymmetric Michael reaction of β-keto esters with nitroolefins to obtain the corresponding chiral Michael adducts with both high chemical yields (up to 99 %) and high stereoselectivities (up to dr = 91:9, up to 91 % ee).",
keywords = "2-Azanorbornane, Amino alcohols, Asymmetric reaction, Michael addition, Organocatalyst",
author = "Rei Togashi 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: A part of this research is partially supported by the Adaptable & Seam-less Technology Transfer Program through Target-driven R&D from Japan Science and Technology Agency (JST) (AS231Z01382G). Publisher Copyright: {\textcopyright} 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim",
year = "2019",
month = jun,
day = "30",
doi = "10.1002/ejoc.201900308",
language = "English",
volume = "2019",
pages = "3882--3889",
journal = "Justus Liebigs Annalen der Chemie",
issn = "0075-4617",
publisher = "Wiley-VCH Verlag",
number = "24",
}