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科研成果
Palladium-Catalyzed Oxidative C-H/N-H Carbonylation for the Synthesis of β-lactams
Li, W.; Liu, C.; Zhang, H.; Ye, K.; Zhang, G.; Zhang, W.; Duan, Z.; You, S.*; Lei, A.*
Angew. Chem. Int. Ed.
2014,
53,
2443-2446.
Cascade Hydrogenative Dearomatization of Pyridine and Asymmetric aza-Friedel-Crafts Alkylation Reaction
Wang, S.-G.; You, S.-L.*
Angew. Chem. Int. Ed.
2014,
53,
2194-2197.
Direct Catalytic C6 Functionalization of 2,3-Disubstituted Indoles by Scandium Triflate
Liu, H.; Zheng, C.*; You, S.-L.*
J. Org. Chem.
2014,
79,
1047-1055.
Recent development of direct asymmetric functionalization of inert C–H bonds
Zheng, C.; You, S.-L.*
RSC. Adv.
2014,
4,
6173-6214.
Dearomatization of Tryptophols via a Vanadium-Catalyzed Asymmetric Epoxidation and Ring-Opening Cascade
Han, L.; Liu, C.; Zhang, W.*; Shi, X.-X.; You, S.-L.*
Chem. Commun.
2014,
50,
1231-1233.
Ir-Catalyzed Intermolecular Asymmetric Allylic Dearomatization Reaction of Indoles
Zhang, X.; Han, L.; You, S.-L.*
Chem. Sci.
2014,
5,
1059-1063.
N-Alkylation of Indole via Ring-Closing Metathesis/Isomerization/Mannich Cascade under Ruthenium/Chiral Phosphoric Acid Sequential Catalysis
Shi, Y.-C.; Wang, S.-G.; Yin, Q.; You, S.-L.*
Org. Chem. Front.
2014,
1,
39-43.
Chiral Amine Catalyzed Asymmetric Bromocyclization of Tryptamine Derivatives
Cai, Q.; Yin, Q.; You, S.-L.*
Asian J. Org. Chem.
2014,
3,
408-411.
Highly Enantioselective Synthesis of Tetrahydrocarbolines via Iridium-Catalyzed Intramolecular Friedel-Crafts Type Allylic Alkylation Reactions
Xu, Q.-L.; Zhuo, C.-X.; Dai, L.-X.; You, S.-L.*
Org. Lett.
2013,
15,
5909-5911.
DPEN-derived Triazolium Salts Catalyzed Annulation Reactions of a,β-Unsaturated Aldehydes with 1,3-Dicarbonyl Compounds
Jia, M.-Q.; Li, G.-T.; You, S.-L.*
Int. J. Chem.
2013,
2,
283-288.
Enantioselective Chlorocyclization of Indole Derived Benzamides for the Synthesis of Spiro-indolines
Yin, Q.; You, S.-L.*
Org. Lett.
2013,
15,
4266-4269.
Palladium(0)-Catalyzed Intramolecular Dearomative Arylation of Pyrroles
Wu, K.-J.; Dai, L.-X.; You, S.-L.*
Chem. Commun.
2013,
49,
8620-8622.
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