|
Our Work:
|
7. Mu-Wang Chen, Yue Ji, Jie Wang, Qing-An Chen, Lei Shi and Yong-Gui Zhou.* Asymmetric Hydrogenation of Isoquinolines and Pyridines Using Hydrogen Halide Generated in situ as Activator. Org. Lett. 2017, 19, 4988-4991. |
|
6. Yue Ji, Lei Shi,* Mu-Wang Chen, Guang-Shou Feng and Yong-Gui Zhou.* Concise Redox De- racemization of Secondary and Tertiary Amines with a Tetrahydroisoquinoline Core via a Nonenzymatic Process. J. Am. Chem. Soc. 2015, 137, 10496-10499. |
|
5. Lei Shi,* Yue Ji, Wen-Xue Huang and Yong-Gui Zhou.* Application of Chiral Anion Metathesis Strategy in Asymmetric Transfer Hydrogenation of Isoquinolines. Acta Chim. Sinica 2014, 72, 820-824. |
|
4. Ran-Ning Guo, Xian-Feng Cai, Lei Shi, Zhi-Shi Ye, Mu-Wang Chen and Yong-Gui Zhou.* An Efficient Route to Chiral N-Heterocycles Bearing C-F Stereogenic Center via Asymmetric Hydrogenation of Fluorinated Isoquinolines. Chem. Commun. 2013, 49, 8537-8539. |
|
|
3. Zhi-Shi Ye, Ran-Ning Guo, Xian-Feng Cai, Mu-Wang Chen, Lei Shi and Yong-Gui Zhou.* Enantio- selective Iridium-Catalyzed Hydrogenation of 1- and 3-Substituted Isoquinolinium Salts. Angew. Chem. Int. Ed. 2013, 52, 3685-3689. <Highlighted by Angew. Chem. Int. Ed. 2013, 52, 9616 > |
|
|
2. Lei Shi, Zhi-Shi Ye, Liang-Liang Cao, Ran-Ning Guo, Yue Hu and Yong-Gui Zhou.* Enantioselective Iridium-Catalyzed Hydrogenation of 3,4-Disubstituted Isoquinolines. Angew. Chem. Int. Ed. 2012, 51, 8286-8289. <Highlighted by Synfacts 2012, 1226 > <Highlighted by Angew. Chem. Int. Ed. 2013, 52, 9616 > |
|
1. Sheng-Mei Lu, You-Qing Wang, Xiu-Wen Han, Yong-Gui Zhou.* Asymmetric Hydrogenation of Quinoline and Isoquinolines Acitivated by Chloroformates. Angew. Chem. Int. Ed. 2006, 45, 2260-2263. <Highlighted by SYNFACTS 2006, 582.><Highlighted by Angew. Chem. Int. Ed. 2013, 52, 9616 > |
Others' Work:
|
5. Alexia N. Kim, Aurapat Ngamnithiporn, Eric R. Welin, Martin T. Daiger, Christian U. Grünanger, Michael D. Bartberger, Scott C. Virgil and Brian M. Stoltz.* Iridium-Catalyzed Enantioselective and Diastereoselective Hydrogenation of 1,3-Disubstituted Isoquinolines. ACS Catal. 2020, 10, 3241-3248. |
|
4. Jialin Wen, Renchang Tan, Shaodong Liu, Qingyang Zhao* and Xumu Zhang.* Strong Bronsted Acid Promoted Asymmetric Hydrogenation of Isoquinolines and Quinolines Catalyzed by a Rh–thiourea Chiral Phosphine Complexvia Anion Binding . Chem. Sci. 2016, 7, 3047-3051. |
|
3. Zi-Yuan Ding, Tianli Wang, Yan-Mei He, Fei Chen, Hai-Feng Zhou, Qing-Hua Fan,* Qingxiang Guo,* and Albert S. C. Chan.* Highly Enantioselective Synthesis of Chiral Tetrahydroquinolines and Tetrahydro-isoquinolines by Ruthenium-Catalyzed Asymmetric Hydrogenation in Ionic Liquid. Adv. Synth. Catal. 2013, 355, 3727-3735. |
|
2. Atsuhiro Iimuro, Kenta Yamaji, Sathaiah Kandula, Takuto Nagano, Yusuke Kita, and Kazushi Mashima.* Asymmetric Hydrogenation of Isoquinolinium Salts Catalyzed by Chiral Iridium Complexes: Direct Synthesis for Optically Active 1,2,3,4-Tetrahydroisoquinolines. Angew. Chem. Int. Ed. 2013, 52, 2046-2050. |
|
1. Matthias Eggenstein, Anika Thomas, Jens Theuerkauf, Giancarlo Francio,* and Walter Leitnera.* Highly Efficient and Versatile Phosphine-Phosphoramidite Ligands for Asymmetric Hydrogenation. Adv. Synth. Catal. 2009, 351, 725-732. |
|