Yiming Cao

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.

Core Scaffold‐Inspired Concise Synthesis of Chiral Spirooxindole‐Pyranopyrimidines with Broad‐Spectrum Anticancer Potency

Jia Yao, Xianxing Jiang, Yiming Cao, 2012 .

An efficient reduction of N-substituted carbonylimidazolides into formamides by NaBH4

Xuan Zhou, Yiming Cao, Zhiyong Chen, 2017 .

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.

Bifunctional organocatalytic strategy for inverse-electron-demand Diels-Alder reactions: highly efficient in situ substrate generation and activation to construct azaspirocyclic skeletons.

Shoulei Wang, Xianxing Jiang, Yiming Cao, 2012, Angewandte Chemie.

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

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

Highly enantioselective ring-opening reactions of aziridines with indole and its application in the building of C3-halogenated pyrroloindolines.

Depeng Zhao, Yunxia Ma, Yiming Cao, 2014, Chemistry.

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.

Highly diastereo- and enantioselective Mannich reaction of lactones with N-Boc-aldimines catalyzed by bifunctional rosin-derived amine thiourea catalysts.

Xianxing Jiang, Yiming Cao, Luping Liu, 2010, Chemical communications.

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

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

Differential cardiovascular effects of synthetic peptides derived from endomorphin-1 in anesthetized rats

Hongmei Liu, Yiming Cao, Rui Wang, 2008, Peptides.

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.