Publications List:


Our Work:

5. Ying Duan, Lu Li, Mu-Wang Chen, Chang-Bin Yu, Hong-Jun Fan* and Yong-Gui Zhou.* Homogenous Pd-Catalyzed Asymmetric Hydrogenation of Unprotected Indoles: Scope and Mechanistic Studies. J. Am. Chem. Soc. 2014, 136,7688-7700..

4. Ying Duan, Mu-Wang Chen, Qing-An Chen, Chang-Bin Yu and Yong-Gui Zhou.* Pd-Catalyzed Asymmetric Hydrogenation of 3-(Toluenesulfonamidoalkyl)indoles. Org. Biomol. Chem. 2012, 10, 1235-1238.

3. Ying Duan, Mu-Wang Chen, Zhi-Shi Ye, Duo-Sheng Wang, Qing-An Chen, and Yong-Gui Zhou.* An Enantioselective Approach to 2,3-Disubstituted Indolines through Consecutive Bronsted Acid/Pd-Complex-Promoted Tandem Reactions. Chem. Eur. J. 2011, 17, 7193-7197.

2. Duo-Sheng Wang, Jie Tang, Yong-Gui Zhou,* Mu-Wang Chen, Chang-Bin Yu, Ying Duan and Guo-Fang Jiang.* Dehydration triggered asymmetric hydrogenation of 3-(a-hydroxyalkyl)indoles. Chem. Sci. 2011, 2, 803-806.

1. Duo-Sheng Wang, Qing-An Chen, Wei Li, Chang-Bin Yu, Yong-Gui Zhou,* and Xumu Zhang* Pd-Catalyzed Asymmetric Hydrogenation of Unprotected Indoles Activated by Bronsted Acids. J. Am. Chem. Soc. 2010, 132, 8909-8911.

Other's Work:

14. Taichiro Touge* and Takayoshi. Ara Asymmetric Hydrogenation of Unprotected Indoles Catalyzed by η6-Arene/N-Me-sulfonyldiamine-Ru(II) Complexes. J. Am. Chem. Soc. 2016, 138, 11299-11305.

13. Zhusheng Yang, Fei Chen,* Yanmei He, Nianfa Yang, and Qing-Hua Fan.* Highly Enantioselective Synthesis of Indolines: Asymmetric Hydrogenation at Ambient Temperature and Pressure with Cationic Ruthenium Diamine Catalysts. Angew. Chem. Int. Ed. 2016, 55, 13863-13866.

12. Lin Chen, Chao Wang,* Li Zhou and Jian Sun.* Chiral 2,3-Disubstituted Indolines from Indoles and Aldehydes by Organocatalyzed Tandem Synthesis Involving Reduction by Trichlorosilane. Adv. Synth. Catal. 2014, 356, 2224-2230.

11. Sergey E. Lyubimov,* Dmitry V. Ozolin, Vadim A. Davankov. Asymmetric Iiridium-Catalyzed Hydrogenation of 2-Methylindole Using Phosphite Ligand, Tetrahedron Lett. 2014, 55, 3613-3614 .

10. José Luis Núez-Rico, Héctor Fernández-Pérez, Anton Vidal-Ferran.* Asymmetric Hydrogenation of Unprotected Indoles Using Iridium Complexes Derived from P–OP Ligands and (reusable) Bronsted Acids, Green Chem. 2014, 16, 1153-1157 .

9. Chao Li , Jianzhong Chen, Guanghong Fu , Delong Liu, Yangang Liu*, Wanbin Zhang.* Highly Enantioselective Hydrogenation of N-unprotected Indoles Using (S)-C10-BridgePHOS as the Chiral Ligand, Tetrahedron 2013, 69, 6839-6844.

8. You-Cai Xiao, Chao Wang, Yuan Yao, Jian Sun and Ying-Chun Chen.* Direct Asymmetric Hydrosilylation of Indoles: Combined Lewis Base and Bronsted Acid Activation. Angew. Chem. Int. Ed. 2011, 50, 10661 –10664.

7. Anna M. Maj, Isabelle Suisse, Catherine Méliet and Francine Agbossou-Niedercorn.* Enantioselective Hydrogenation of Indoles Derivatives Catalyzed by Walphos/Rhodium Complexes, Tetrahedron: Asymmetry 2010, 21, 2010–2014.

6.Nataša Mršić, Thomas Jerphagnon , Adriaan J. Minnaard,* Ben L. Feringa,* Johannes G. de Vries.* Asymmetric Hydrogenation of 2-substituted N-protected-indoles Catalyzed by Rhodium Complexes of BINOL-derived Phosphoramidites. Tetrahedron: Asymmetry 2010, 7–10.

5. Alejandro Baeza and Andreas Pfaltz*. Iridium-Catalyzed Asymmetric Hydrogenation of N-Protected Indoles. Chem. Eur. J. 2010, 16, 2036–2039.

4. Ryoichi Kuwano,* Manabu Kashiwabara, Koji Sato, Takashi Ito, Kohei Kaneda and Yoshihiko Ito. Catalytic Asymmetric Hydrogenation of Indoles Using a Rhodium Complex with a Chiral Bisphosphine Ligand PhTRAP. Tetrahedron: Asymmetry 2006, 17, 521–535.

3. Ryoichi Kuwano* and Manabu Kashiwabara. Ruthenium-Catalyzed Asymmetric Hydrogenation of N-Boc-Indoles. Org. Lett. 2006, 8, 2653-2655.

2. Ryoichi Kuwano,* Kohei Kaneda, Takashi Ito, Koji Sato, Takashi Kurokawa, and Yoshihiko Ito.* Highly Enantioselective Synthesis of Chiral 3-Substituted Indolines by Catalytic Asymmetric Hydrogenation of Indoles. Org. Lett. 2004, 6, 2213-2215.

1. Ryoichi Kuwano,* Koji Sato, Takashi Kurokawa, Daisuke Karube, and Yoshihiko Ito.* Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles. J. Am. Chem. Soc. 2000, 122, 7614-7615.



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