2018年
A novel proline-based acridone bifunctional organocatalyst for the asymmetric michael addition of cyclohexanone
Chemistry Letters
- ,
- 巻
- 47
- 号
- 4
- 開始ページ
- 472
- 終了ページ
- 474
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1246/cl.171220
- 出版者・発行元
- Chemical Society of Japan
The rigid and planar acridone moiety was successfully linked with a chiral pyrrolidine template through an amide bond to develop a novel organocatalyst. This organocatalyst competently promotes the asymmetric Michael addition of cyclohexanone to nitroolefins with anisole, naphthalene, and heterocyclic aromatic rings under neat conditions. In this novel approach, the acridone moiety proved effective in chiral organocatalysis.
- リンク情報
- ID情報
-
- DOI : 10.1246/cl.171220
- ISSN : 1348-0715
- ISSN : 0366-7022
- SCOPUS ID : 85044318230