Use of β-Amido Allylboronate as a Nucleophilic Reagent in Catalytic Enantioselective Addition to Isatins
Tetsuya Sengoku, Akihiro Sugiyama, Yuta Kamiya, Ryunosuke Maegawa, Masaki Takahashi and Hidemi Yoda
European Journal of Organic Chemistry, 2017, 1285-1288. ()
A new catalytic system that enables the enantioselective tin-free “amide allylation” of isatins is developed with the aid of a newly prepared (β-amidoallyl)boronate.
![](https://wwp.shizuoka.ac.jp/lab-o-chem/wp-content/uploads/sites/84/2017/03/86.jpg)
Journal Information: Impact factor 3.068 (Q2, JCR 2015)