1593933-15-3Relevant articles and documents
Asymmetric michael addition of oxindoles to allenoate catalyzed by N-acyl aminophosphine: Construction of functionalized oxindoles with quaternary stereogenic center
Chen, Jinhao,Cai, Yuepeng,Zhao, Gang
, p. 359 - 363 (2014)
A novel reaction between ethyl allenoate and oxindoles that enables the asymmetric synthesis of 3,3-bisubstituted oxindoles with our previously established bifunctional N-acyl aminophosphine catalysts is reported. These products bearing a chiral quaternary carbon center at the C-3 position of the oxindoles may have potential significance in the synthesis of related structures. The best performance of these processes provides adducts with 92% yield and 94% ee.