Jin‐Quan Yu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Jin‐Quan Yu has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
Ramesh Giri
Department of Chemistry MS015, Brandeis University, Waltham, Massachusetts, USA
5 shared publicationsXiao Chen
Department of Chemistry MS015, Brandeis University, Waltham, Massachusetts, USA
5 shared publicationsBruce M. Foxman
Department of Chemistry, Brandeis University, Waltham, MA 02454-9110, USA, Fax: (+1) 781-736-2516
2 shared publicationsChengyun Guo
Department of Chemistry, Brandeis University, Waltham, MA 02454-9110, USA, Fax: (+1) 781-736-2516
2 shared publicationsDong‐Hui Wang
Department of Chemistry, Brandeis University, Waltham, MA 02454-9110, USA, Fax: (+1) 781-736-2516
2 shared publicationsJian‐Guang Lei
Department of Chemistry, Brandeis University, Waltham, MA 02454-9110, USA, Fax: (+1) 781-736-2516
2 shared publications
Latest Publications
- 16 October 2006
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 4 (22) , 4041-4047
σ-Chelation-directed C–H functionalizations using Pd( ii ) and Cu( ii ) catalysts: regioselectivity, stereoselectivity and catalytic turnover
Recent progress in σ-chelation directed C–H functionalization from the authors' group is described to illustrate the challenges and opportunities in the development of synthetically-useful catalytic reactions involving C–H activation as the key step. Emphasis is placed on strategies for developing catalysis under mild conditions and controlling regio- and stereoselectivity.
- 16 October 2006
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 4 (22) , 4041-4047
σ-Chelation-directed C–H functionalizations using Pd( ii ) and Cu( ii ) catalysts: regioselectivity, stereoselectivity and catalytic turnover
Recent progress in σ-chelation directed C–H functionalization from the authors' group is described to illustrate the challenges and opportunities in the development of synthetically-useful catalytic reactions involving C–H activation as the key step. Emphasis is placed on strategies for developing catalysis under mild conditions and controlling regio- and stereoselectivity.
- Top Cited Papers
- 16 November 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (45) , 7420-7424
Pd‐Catalyzed Stereoselective Oxidation of Methyl Groups by Inexpensive Oxidants under Mild Conditions: A Dual Role for Carboxylic Anhydrides in Catalytic C-H Bond Oxidation
- 16 November 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (45) , 7420-7424
Top Cited PapersPd‐Catalyzed Stereoselective Oxidation of Methyl Groups by Inexpensive Oxidants under Mild Conditions: A Dual Role for Carboxylic Anhydrides in Catalytic C-H Bond Oxidation
- 16 November 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (45) , 7586-7590
Pd‐Catalyzed Stereoselective Oxidation of Methyl Groups by Inexpensive Oxidants under Mild Conditions: A Dual Role for Carboxylic Anhydrides in Catalytic C-H Bond Oxidation
- 16 November 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (45) , 7586-7590
Pd‐Catalyzed Stereoselective Oxidation of Methyl Groups by Inexpensive Oxidants under Mild Conditions: A Dual Role for Carboxylic Anhydrides in Catalytic C-H Bond Oxidation
- Top Cited Papers
- 22 March 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (14) , 2112-2115
Palladium‐Catalyzed Asymmetric Iodination of Unactivated C-H Bonds under Mild Conditions
- 22 March 2005
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (14) , 2112-2115
Top Cited PapersPalladium‐Catalyzed Asymmetric Iodination of Unactivated C-H Bonds under Mild Conditions
- 22 March 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (14) , 2150-2153
Palladium-Catalyzed Asymmetric Iodination of Unactivated C?H Bonds under Mild Conditions
- 22 March 2005
- Published by Wiley in Angewandte Chemie
- Vol. 117 (14) , 2150-2153
Palladium-Catalyzed Asymmetric Iodination of Unactivated C?H Bonds under Mild Conditions