F. Shen

发表

A unique approach to the concise synthesis of highly optically active spirooxazolines and the discovery of a more potent oxindole-type phytoalexin analogue.

Xianxing Jiang, Yiming Cao, Yiqing Wang, 2010, Journal of the American Chemical Society.

Catalytic asymmetric 1,2-addition of α-isothiocyanato phosphonates: synthesis of chiral β-hydroxy- or β-amino-substituted α-amino phosphonic acid derivatives.

Yiming Cao, F. Shen, Rui Wang, 2014, Angewandte Chemie.

Enantioselective Michael/cyclization reaction sequence: scaffold-inspired synthesis of spirooxindoles with multiple stereocenters.

Xianxing Jiang, Yiming Cao, Luping Liu, 2011, Angewandte Chemie.

Catalytic enantioselective ring-opening reaction of meso-aziridines with α-isothiocyanato imides.

Yiming Cao, F. Shen, Rui Wang, 2013, Chemistry.

Catalytic asymmetric Michael addition/cyclization of isothiocyanato oxindoles: highly efficient and versatile approach for the synthesis of 3,2'-pyrrolidinyl mono- and bi-spirooxindole frameworks.

Yiming Cao, F. Shen, Rui Wang, 2013, Chemistry.

Direct organocatalytic asymmetric aldol reaction of alpha-isothiocyanato imides to alpha-ketoesters under low ligand loading: a doubly stereocontrolled approach to cyclic thiocarbamates bearing chiral quaternary stereocenters.

Xianxing Jiang, Yiming Cao, F. Shen, 2010, Organic letters.

Enantioselective Michael/cyclization reaction sequence: scaffold-inspired synthesis of spirooxindoles with multiple stereocenters.

Xianxing Jiang, Yiming Cao, Luping Liu, 2011, Angewandte Chemie.

Enantioselective Michael/cyclization reaction sequence: scaffold-inspired synthesis of spirooxindoles with multiple stereocenters.

Xianxing Jiang, Yiming Cao, Luping Liu, 2011, Angewandte Chemie.

A unique approach to the concise synthesis of highly optically active spirooxazolines and the discovery of a more potent oxindole-type phytoalexin analogue.

Xianxing Jiang, Yiming Cao, Yiqing Wang, 2010, Journal of the American Chemical Society.