Year 2013

Posted in 2013 on 十二月 3rd, 2012 by Delta – 评论关闭
  • Xu, Q.-L.; Zhuo, C.-X.; Dai, L.-X.; You, S.-L.* Highly Enantioselective Synthesis of Tetrahydrocarbolines via Iridium-Catalyzed Intramolecular Friedel–Crafts Type Allylic Alkylation Reactions. Org. Lett. 2013, 15, 5909-5911.
  • Shi, Y.-C.; Yang, R.-F.; Gao, D.-W.; You, S.-L.* Enantioselective synthesis of planar chiral ferrocenes via palladium-catalyzed annulation with diarylethynes. Beilstein J. Org. Chem. 2013, 9, 1891-1896.
  • Jia, M.-Q.; Li, G.-T.; You, S.-L.* DPEN-derived Triazolium Salts Catalyzed Annulation Reactions of a,β-Unsaturated Aldehydes with 1,3-Dicarbonyl Compounds. Int. J. Chem. (IBH, Mumbai) 2013, 2, 283-288.
  • Wu, K.-J.; Dai, L.-X.; You, S.-L.* Palladium(0)-catalyzed intramolecular dearomative arylation of pyrroles. Chem. Commun. 2013, 49, 8620-8622.
  • Zhuo, C.-X.; You, S.-L.* Palladium-Catalyzed Intermolecular Asymmetric Allylic Dearomatization Reaction of Naphthol Derivatives. Angew. Chem. Int. Ed. 2013, 52, 10056-10059.
  • Yin, Q.; You, S.-L.* Enantioselective Chlorocyclization of Indole Derived Benzamides for the Synthesis of Spiro-indolines. Org. Lett. 2013, 15, 4266-4269.
  • Zhang, J.-W.; Cai, Q.; Gu, Q.; Shi, X.-X.; You, S.-L.* Enantioselective synthesis of benzofurans and benzoxazines via an olefin cross-metathesis–intramolecular oxo-Michael reaction. Chem. Commun. 2013, 49, 7750-7752.
  • Zhang, X.; Liu, W.-B.; Wu, Q.-F.; You, S.-L.* Ruthenium-Catalyzed Intramolecular Allylic Dearomatization Reaction of Indole Derivatives. Org. Lett. 2013, 15, 3746-3749.
  • Zhang, X.; Yang, Z.-P.; Liu, C.; You, S.-L.* Ru-Catalyzed Intermolecular Dearomatization Reaction of Indoles with Allylic Alcohols. Chem. Sci. 2013, 4, 3239-3243.
  • Ye, K.-Y.; Zhao, Z.-A.; Lai, Z.-W.; Dai, L.-X.; You, S.-L.* Highly Regioselective Allylic Substitution Reactions Catalyzed by an Air-stable (π-Allyl)iridium Complex Derived from Dinaphthocyclooctatetraene and a Phosphoramidite Ligand Synthesis 2013, 2109-2114. (invited paper for Special Topics Issue on Iridium catalysis in chemical synthesis, editor: Prof. Erick M. Carreira)
  • Zhuo, C.-X.; Wu, Q.-F.; Zhao, Q.; Xu, Q.-L.; You, S.-L.* Enantioselective Functionalization of Indoles and Pyrroles via An in-situ Formed Spiro-intermediate. J. Am. Chem. Soc. 2013, 135, 8169-8172.
  • Yin, Q.; Wang, S.-G.; You, S.-L.* Asymmetric Synthesis of Tetrahydro-β-carbolines via Chiral Phosphoric Acid Catalyzed Transfer Hydrogenation Reaction. Org. Lett. 2013, 11, 2688-2691.
  • Jia, M.-Q.; You, S.-L.* Desymmetrization of Cyclohexadienones via Intramolecular Stetter Reaction to Construct Tricyclic Carbocycles. Synlett 2013, 24, 1201-1204. (Invited Cluster Reports. Topic: Carbene Catalysis. Regional Editor: Tomislav Rovis)
  • Zheng, C.*; Wu, Q.-F.; You, S.-L.* A Combined Theoretical and Experimental Investigation into the Highly Stereoselective Migration of Spiroindolenines. J. Org. Chem. 2013, 78, 4357-4365.
  • Wang, S.-G.; Zhang, W.; You, S.-L.* Construction of Spiro-tetrahydroquinolines via Intramolecular Dearomatization of Quinolines: Free of a Preinstalled Activation Group. Org. Lett. 2013, 15, 1488-1491.
  • Jia, M.-Q.; You, S.-L.* N-Heterocyclic Carbene-Catalyzed Enantioselective Intramolecular N-Tethered Aldehyde-Ketone Benzoin Reactions. ACS Catal. 2013, 3, 622-624.
  • Ye, K.-Y.; Dai, L.-X.; You, S.-L.* Synthesis of 1Z,4E,6E-Triene Derivatives by Chemo- and Regioselective Iridium-Catalyzed Dienylation of ortho-Aminostyrenes with Dienyl Carbonates. Asian J. Org. Chem. 2013, 2, 244-249.
  • Cai, Q.; Liang, X.-W.; Wang, S.-G.; You, S.-L.* An olefin isomerization/asymmetric Pictet–Spengler cascade via sequential catalysis of ruthenium alkylidene and chiral phosphoric acid. Org. Biomol. Chem. 2013, 11, 1602-1605.
  • Gao, D.-W.; Shi, Y.-C.; Gu, Q.*; Zhao, Z.-L.; You, S.-L.* Enantioselective Synthesis of Planar Chiral Ferrocenes via Palladium-catalyzed Direct Coupling with Aryl Boronic Acids. J. Am. Chem. Soc. 2013, 135, 86-89.
  • Xu, Q.-L.; Dai, L.-X.; You, S.-L.* Diversity oriented synthesis of indole-based peri-annulated compounds via allylic alkylation reactions. Chem. Sci. 2013, 4, 97-102.