Amino amide organocatalysts for asymmetric michael addition of β-Keto esters with β-nitroolefins

Isiaka Alade Owolabi, Madhu Chennapuram, Chigusa Seki, Yuko Okuyama, Eunsang Kwon, Koji Uwai, Michio Tokiwa, Mitsuhiro Takeshita, Hiroto Nakano

研究成果: Article査読

2 被引用数 (Scopus)

抄録

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).

本文言語English
ページ(範囲)696-701
ページ数6
ジャーナルBulletin of the Chemical Society of Japan
92
3
DOI
出版ステータスPublished - 2019

ASJC Scopus subject areas

  • Chemistry(all)

フィンガープリント 「Amino amide organocatalysts for asymmetric michael addition of β-Keto esters with β-nitroolefins」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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