Wei‐Cheng Yuan - Concepedia

Author

Wei‐Cheng Yuan

Also Known As

Mei Bai, Nan-Wei Wan, Wei-Cheng Yuan, Wei-cheng Yuan, Weicheng Yuan, Wei‐Cheng Yuan, Ying Zhou, Yong You, Yu Cao, Yuan, Wei-Cheng

425

Publications

Citations

H-Index

Concepts

All Affiliations

Chengdu Organic Chemicals (China)Chinese Academy of Sciences University of Chinese Academy of Sciences Chengdu University Chengdu Institute of Biology

About

Wei‐Cheng Yuan is an author at Chengdu Organic Chemicals (China) specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	42	112	5.2K
2	Biomolecular Engineering	36	77	3.8K
3	Natural Sciences	32	60	2.7K
4	Biochemistry	11	13	613
5	Medicine	1	1	26

Wei‐Cheng Yuan

186

Publications

8.5K

Citations

H-Index

Page 1

	Year	Citations
Highly Enantioselective Construction of Spiro[<i>4H</i>-pyran-3,3′-oxindoles] Through a Domino Knoevenagel/Michael/Cyclization Sequence Catalyzed by Cupreine Wenbing Chen, Zhijun Wu, Qing‐Lan Pei, Organic Letters	2010	300
Catalytic Asymmetric Diamination of Conjugated Dienes and Triene Haifeng Du, Wei‐Cheng Yuan, Baoguo Zhao, Journal of the American Chemical Society Chemical EngineeringEngineeringCatalytic SynthesisOrganic ChemistryOrganometallic Catalysis	2007	246
Carbonyl catalysis enables a biomimetic asymmetric Mannich reaction Jianfeng Chen, Xing Gong, Jianyu Li, Science	2018	225
Organocatalytic Direct Asymmetric Aldol Reactions of 3-Isothiocyanato Oxindoles to Ketones: Stereocontrolled Synthesis of Spirooxindoles Bearing Highly Congested Contiguous Tetrasubstituted Stereocenters Wenbing Chen, Zhijun Wu, Jing Hu, Organic Letters Asymmetric CatalysisNovel OrganocatalystsEngineeringStereocontrolled SynthesisBiochemistry	2011	192
A Pd(0)-Catalyzed Diamination of Terminal Olefins at Allylic and Homoallylic Carbons via Formal C−H Activation under Solvent-Free Conditions Haifeng Du, Wei‐Cheng Yuan, Baoguo Zhao, Journal of the American Chemical Society Chemical EngineeringNovel Diamination ProcessEngineeringCross-coupling ReactionCatalytic Synthesis	2007	170
Highly Efficient and Stereocontrolled Construction of 3,3′-Pyrrolidonyl Spirooxindoles via Organocatalytic Domino Michael/Cyclization Reaction Xiong‐Li Liu, Wen‐Yong Han, Xiaomei Zhang, Organic Letters	2013	159
Highly Enantioselective [3+2] Coupling of Indoles with Quinone Monoimines Promoted by a Chiral Phosphoric Acid Lihua Liao, Chang Shu, Minmin Zhang, Angewandte Chemie International Edition	2014	156
FeCl<sub>3</sub>-Catalyzed Stereoselective Construction of Spirooxindole Tetrahydroquinolines via Tandem 1,5-Hydride Transfer/Ring Closure Yanyan Han, Wen‐Yong Han, Xue Hou, Organic Letters	2012	147
Asymmetric Michael/Cyclization Cascade Reaction of 3-Isothiocyanato Oxindoles and 3-Nitroindoles with Amino-Thiocarbamate Catalysts: Enantioselective Synthesis of Polycyclic Spirooxindoles Jian‐Qiang Zhao, Ming‐Qiang Zhou, Zhijun Wu, Organic Letters Asymmetric CatalysisEngineeringPolycyclic SpirooxindolesHeterocyclicContiguous Chiral Centers	2015	141
Organocatalytic Asymmetric Michael Addition of Pyrazolin‐5‐ones to Nitroolefins with Bifunctional Thiourea: Stereocontrolled Construction of Contiguous Quaternary and Tertiary Stereocenters Yu‐Hua Liao, Wenbing Chen, Zhijun Wu, Advanced Synthesis & Catalysis Novel OrganocatalystsDiversity Oriented SynthesisDerivativesPyrazolin‐5‐one DerivativesEngineering	2010	129

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