Publication

Year 2017

Posted in 2017 on 一月 10th, 2017 by Delta – 评论关闭
  • Cheng, Q.; Zhang, H.-J.; Yue, W.-J.; You, S.-L.* Palladium-Catalyzed Highly Stereoselective Dearomative [3 + 2] Cycloaddition of Nitrobenzofurans. Chem 2017, 3, 428-436.
  • Shao, W.; You, S.-L.* Highly Diastereo- and Enantioselective Synthesis of Tetrahydro-5H-Indolo[2,3-b]quinolines through Copper-Catalyzed Propargylic Dearomatization of Indoles. Chem. Eur. J. 2017, Early View.
  • Huang, L.; Cai, Y.; Zheng, C.; Dai, L.-X.; You, S.-L*. Iridium-Catalyzed Enantioselective Synthesis of Pyrrole-Annulated Medium-Sized-Ring Compounds. Angew. Chem. Int. Ed. 2017, 56, 10545-10548.
  • Glavac, D.; Zheng, C.; Dokli, I.; You, S.-L.*; Gredicak, M.* Chiral Brønsted Acid Catalyzed Enantioselective aza-Friedel–Crafts Reaction of Cyclic α-Diaryl N-Acyl Imines with Indoles. J. Org. Chem. 2017, 82, 8752-8760.
  • Xu, R.-Q.; Yang, P.; You, S.-L.* Pd(0)-Catalyzed intramolecular arylative dearomatization of β-naphthols. Chem. Commun. 2017, 53, 7553-7556.
  • Xu, R.-Q.; Gu, Q.; You, S.-L.* Construction of Chiral Tetrahydro-β-Carbolines: Asymmetric Pictet–Spengler Reaction of Indolyl Dihydropyridines. Angew. Chem. Int. Ed. 2017, 56, 7252-7256.
  • Wang, S.-G.; Xia, Z.-L.; Xu, R.-Q.; Liu, X.-J.; Zheng, C.; You, S.-L.* Construction of Chiral Tetrahydro-β-Carbolines: Asymmetric Pictet–Spengler Reaction of Indolyl Dihydropyridines. Angew. Chem. Int. Ed. 2017, 56, 7440-7443.
  • Wang, S.-B.; Gu, Q.; You, S.-L.* Rhodium(III)-Catalyzed C–H Alkynylation of Ferrocenes with Hypervalent Iodine Reagents. J. Org. Chem. 2017, ASAP.
  • Liang, X.-W.; Liu, C.; Zhang, W.; You, S.-L.* Asymmetric fluorinative dearomatization of tryptamine derivatives. Chem. Commun. 2017, 53, 5531-5534.
  • Zheng, J.; Wang, S.-B.; Zheng, C.; You, S.-L.* Asymmetric Synthesis of Spiropyrazolones by Rhodium-Catalyzed C(sp2)−H Functionalization/Annulation Reactions. Angew. Chem. Int. Ed. 2017, 56, 4540-4544.
  • Liu, X.-J.; You, S.-L.* Enantioselective Iridium-Catalyzed Allylic Substitution with 2-Methylpyridines. Angew. Chem. Int. Ed. 2017, 56, 4002-4005.
  • Li, G.-T.; Li, Z.-K.; Gu, Q.; You, S.-L.* Asymmetric Synthesis of 4-Aryl-3,4-dihydrocoumarins by N-Heterocyclic Carbene Catalyzed Annulation of Phenols with Enals. Org. Lett. 2017, 19, 1318-1321.
  • Liu, C.; Yi, J.-C.; Dai, L.-X.; You, S.-L.* Copper(I)-Catalyzed Cascade Dearomatization of Tryptophols with 3-Indolylphenyliodonium Salts. Asian J. Org. Chem. 2017, DOI: 10.1002/ajoc.201600626.
  • Zhou, Y.; Xia, Z.-L.; Gu, Q.; You, S.-L.* Chiral Phosphoric Acid Catalyzed Intramolecular Dearomative Michael Addition of Indoles to Enones. Org. Lett. 2017, 19, 762-765.
  • Gao, D.-W.; Gu, Q.; Zheng, C.; You, S.-L.* Synthesis of Planar Chiral Ferrocenes via Transition-Metal-Catalyzed Direct C–H Bond Functionalization. Acc. Chem. Res. 2017, 50, 351-365.
  • Yang, Z.-P.; Zheng, C.; Huang, L.; Qian, C.; You, S.-L.* Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization Reaction of Benzoxazoles, Benzothiazoles, and Benzimidazoles. Angew. Chem. Int. Ed. 2017, 56, 1530-1534.
  • Tu, H.-F.; Zheng, C.; Xu, R.-Q.; Liu, X.-J.; You, S.-L.* Iridium-Catalyzed Intermolecular Asymmetric Dearomatization of β-Naphthols with Allyl Alcohols or Allyl Ethers. Angew. Chem. Int. Ed. 2017, 56, 3237-3241.
  • Ye, K.-Y.; Wu, K.-J.; Li, G.-T.; Dai, L.-X.; You, S.-L.* Synthesis of Enantioenriched Indolopiperazinones via Iridium(I) N-Heterocyclic Carbene Complex Catalyzed Asymmetric Intramolecular Allylic Amination Reaction. Hetereocycles 2017, 95, 304-313.

Year 2016

Posted in 2016 on 十二月 16th, 2015 by Delta – Be the first to comment
  • Zheng, C.; You, S.-L.* Catalytic Asymmetric Dearomatization by Transition-Metal Catalysis: A Method for Transformations of Aromatic Compounds. Chem 2016, 1, 830-857.
  • Xu, R.-Q.; Yang, P.; Tu, H.-F.; Wang, S.-G.; You, S.-L.* Palladium(0)-Catalyzed Intermolecular Arylative Dearomatization of β-Naphthols. Angew. Chem. Int. Ed. 2016, 55, 15137-15141 .
  • Wang, D.-C.; Xie, M.-S.; Guo, H.-M.*; Qu, G.-R.; Zhang, M.-C.; You, S.-L.* Enantioselective Dearomative [3+2] Cycloaddition Reactions of Benzothiazoles. Angew. Chem. Int. Ed. 2016, 55, 14111-14115.
  • Gao, D.-W.; Gu, Y.; Wang, S.-B.; Gu, Q.*; You, S.-L.* Palladium(0)-Catalyzed Asymmetric C–H Alkenylation for Efficient Synthesis of Planar Chiral Ferrocenes. Organometallics 2016, 35, 3227-3233.
  • Gao, R.-D.; Xu, Q.-L.; Dai, L.-X.; You, S.-L.* Pd-Catalyzed Cascade Allylic Alkylation and Dearomatization Reactions of Indoles with Vinyloxirane. Org. Biomol. Chem. 2016, 14, 8044-8046.
  • Zhang, X.; Liu, W.-B.; Cheng, Q.; You, S.-L.* Iridium-Catalyzed Asymmetric Allylic Amination Reactions with N-Aryl Phosphoramidite Ligands. Organometallics 2016, 35, 2467-2472.
  • Gao, R.-D.; Xu, Q.-L.; Zhang, B.; Gu, Y.; Dai, L.-X.; You, S.-L.* Palladium(0)-Catalyzed Intermolecular Allylic Dearomatization of Indoles by a Formal [4+2] Cycloaddition Reaction. Chem. Eur. J. 2016, 22, 11601-11604.
  • Zhuo, C.-X.; Zhang, X.; You, S.-L.* Enantioselective Synthesis of Pyrrole-Fused Piperazine and Piperazinone Derivatives via Ir-Catalyzed Asymmetric Allylic Amination. ACS Catal. 2016, 6, 5307-5310.
  • Liang, X.-W.; Zheng, C.; You, S.-L.* Dearomatization through Halofunctionalization Reactions. Chem. Eur. J. 2016, 22, 11918-11913.
  • Liu, C.; Yi, J.-C.; Liang, X.-W.; Xu, R.-Q.; Dai, L.-X.; You, S.-L.* Copper(I)-Catalyzed Asymmetric Dearomatization of Indole Acetamides with 3-Indolylphenyliodonium Salts. Chem. Eur. J. 2016, 22, 10813-10816.
  • Liang, X.-W.; Zheng, C.; You, S.-L.* Catalytic Asymmetric Chlorinative Dearomatization Reaction of Benzofurans. Adv. Synth. Catal. 2016, 358, 2066-2071.
  • Ye, K.-Y.; Cheng, Q.; Zhuo, C.-X.; Dai, L.-X.; You, S.-L.* An Iridium(I) N-Heterocyclic Carbene Complex Catalyzes Asymmetric Intramolecular Allylic Amination Reactions. Angew. Chem. Int. Ed. 2016, 55, 8113-8116.
  • Zhao, Z.-L.; Gu, Q.; Wu, X.-Y.*; You, S.-L* Enantioselective synthesis of 10-allylanthrones via iridium-catalyzed allylic substitution reaction. Chin. Chem. Lett. 2016, 27, 619-622.
  • Huang, L.; Dai, L.-X.; You, S.-L.* Enantioselective Synthesis of Indole-Annulated Medium-Sized Rings. J. Am. Chem. Soc. 2016, 138, 5793-5796.
  • Zheng, J.; Cui, W.-J.; Zheng, C.; You, S.-L.* Synthesis and Application of Chiral Spiro Cp Ligands in Rhodium-Catalyzed Asymmetric Oxidative Coupling of Biaryl Compounds with Alkenes. J. Am. Chem. Soc. 2016, 138, 5242-5245.
  • Wu, Q.-F.; Zheng, C.*; Zhuo, C.-X.; You, S.-L.* Highly efficient synthesis and stereoselective migration reactions of chiral five-membered aza-spiroindolenines: scope and mechanistic understanding. Chem. Sci. 2016, 7, 4453-4459.
  • Wang, S.-B.; Zheng, J.; You, S.-L.* Synthesis of Ferrocene-Based Pyridinones through Rh(III)-Catalyzed Direct C–H Functionalization Reaction. Organometallics 2016, 35, 1420-1425.
  • Gao, D.-W.; Gu, Q.; You, S.-L.* An Enantioselective Oxidative C–H/C–H Cross-Coupling Reaction: Highly Efficient Method To Prepare Planar Chiral Ferrocenes. J. Am. Chem. Soc. 2016, 138, 2544-2547.
  • Wu, W.-T.; Xu, R.-Q.; Zhang, L.*; You, S.-L.* Construction of spirocarbocycles via gold-catalyzed intramolecular dearomatization of naphthols. Chem. Sci. 2016, 7, 3427-3431.
  • Cheng, Q.; Wang, Y.; You, S.-L.* Chemo-, Diastereo-, and Enantioselective Iridium-Catalyzed Allylic Intramolecular Dearomatization Reaction of Naphthol Derivatives. Angew. Chem. Int. Ed. 2016, 55, 3496-3499.
  • Wu, W.-T.; Zhang, L.*; You, S.-L.* Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives. Chem. Soc. Rev. 2016, 45, 1570-1580.
  • Zheng, C.*; Zheng, J.; You, S.-L.* A DFT Study on Rh-Catalyzed Asymmetric Dearomatization of 2-Naphthols Initiated with C–H Activation: A Refined Reaction Mechanism and Origins of Multiple Selectivity. ACS Catal. 2016, 6, 262-271.
  • Liu, C.; Yi, J.-C.; Zheng, Z.-B.; Tang, Y.*; Dai, L.-X.; You, S.-L.* Enantioselective Synthesis of 3a-Amino-Pyrroloindolines by Copper-Catalyzed Direct Asymmetric Dearomative Amination of Tryptamines. Angew. Chem. Int. Ed. 2016, 55, 751-754.
  • Zhou, Y.; Liu, X.-W.; Gu, Q.; You, S.-L.* Enantioselective Synthesis of Tetrahydroindolizines via Ruthenium-Chiral Phosphoric Acid Sequential Catalysis. Synlett 2016, 27, 586-590.

Year 2015

Posted in 2015 on 一月 3rd, 2015 by Delta – 评论关闭
  • Yang, Z.-P.; Wu, Q.-F.; Shao, W.; You, S.-L.* Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization Reaction of Pyridines, Pyrazines, Quinolines, and Isoquinolines. J. Am. Chem. Soc. 2015, 137, 15899-15906.
  • Han, L.; Zhang, W.; Shi, X.-X.; You, S.-L.* Dearomatization of Indoles via a Phenol-Directed Vanadium- Catalyzed Asymmetric Epoxidation and Ring-Opening Cascade. Adv. Synth. Catal. 2015, 357, 3064-3068.
  • Wang, S.-G.; Liu, X.-J.; Zhao, Q.-C.; Zheng, C.; Wang, S.-B.; You, S.-L.* Asymmetric Dearomatization of β-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction. Angew. Chem. Int. Ed. 2015, 54, 14929-14932.
  • Zhuo, C.-X.; Zhou, Y.; Cheng, Q.; Huang, L.; You, S.-L.* Enantioselective Construction of Spiroindolines with Three Contiguous Stereogenic Centers and Chiral Tryptamine Derivatives via Reactive Spiroindolenine Intermediates. Angew. Chem. Int. Ed. 2015, 54, 14146-14149.
  • Gao, D.-W.; Zheng, C.; Gu, Q.; You, S.-L.* Pd-Catalyzed Highly Enantioselective Synthesis of Planar Chiral Ferrocenylpyridine Derivatives. Organometallics 2015, 34, 4618-4625.
  • Zhang, X.; Liu, W.-B.; Tu, H.-F.; You, S.-L.* Ligand-Enabled Ir-Catalyzed Intermolecular Diastereoselective and Enantioselective Allylic Alkylation of 3-Substituted Indoles. Chem. Sci. 2015, 6, 4525-4529.
  • Zhuo, C.-X.; Chen, Q.; Liu, W.-B.; Zhao, Q.; You, S.-L.* Enantioselective Synthesis of Pyrrole-Based Spiro- and Polycyclic Derivatives by Iridium-Catalyzed Asymmetric Allylic Dearomatization and Controllable Migration Reactions. Angew. Chem. Int. Ed. 2015, 54, 8475-8479.
  • Li, G.-T.; Gu, Q.; You, S.-L.* Enantioselective annulation of enals with 2-naphthols by triazolium salts derived from L-phenylalanine. Chem. Sci. 2015, 6, 4273-4278.
  • Yin, Q.; Wang, S.-G.; Liang, X.-W.; Gao, D.-W.; Zheng, J.; You, S.-L.* Organocatalytic asymmetric chlorinative dearomatization of naphthols. Chem. Sci. 2015, 6, 4179-4183.
  • Shao, W.; Li, H.; Liu, C.; Liu, C.-J.*; You, S.-L.* Copper-Catalyzed Intermolecular Asymmetric Propargylic Dearomatization of Indoles. Angew. Chem. Int. Ed. 2015, 54, 7684-7687.
  • Zhou, Y.; Zhuo, C.-X.; Gu, Q.; You, S.-L.* Intermolecular Dearomatization Reaction of Pyrroles Promoted by Silica Gel. Adv. Synth. Catal. 2015, 357, 912-916.
  • Zheng, J.; Wang, S.-B.; Zheng, C.; You, S.-L.* Asymmetric Dearomatization of Naphthols via a Rh-Catalyzed C(sp2)–H Functionalization/Annulation Reaction. J. Am. Chem. Soc. 2015, 137, 4880–4883.
  • Liu, C.; Yin, Q.; Dai, L.-X.; You, S.-L.* Synthesis of pyrroloindolines and furoindolines via cascade dearomatization of indole derivatives with carbenium ion. Chem. Commun. 2015, 51, 5971-5974.
  • Zhang, J.-W.; Liu, X.-W.; Gu, Q.; Shi, X.-X.; You, S.-L.* Enantioselective synthesis of 4,5,6,7-tetrahydroindoles via olefin cross-metathesis/intramolecular Friedel–Crafts alkylation reaction of pyrroles. Org. Chem. Front. 2015, 2, 476-480.
  • Zhao, Z.-L.; Xu, Q.-L.; Gu, Q.; Wu, X.-Y.*; You, S.-L.* Enantioselective synthesis of 4-substituted tetrahydroisoquinolines via palladium-catalyzed intramolecular Friedel–Crafts type allylicalkylation of phenols. Org. Biomol. Chem. 2015, 13, 3086-3092.
  • Zhang, X.; Yang, Z.-P.; Hang, L.; You, S.-L.* Highly Regio- and Enantioselective Synthesis of N-Substituted 2-Pyridones: Iridium-Catalyzed Intermolecular Asymmetric Allylic Amination. Angew. Chem. Int. Ed. 2015, 54, 1873-1876.
  • Wang, S.-G.; Yin, Q.; Zhuo, C.-X.; You, S.-L.* Asymmetric Dearomatization of β-Naphthols through an Amination Reaction Catalyzed by a Chiral Phosphoric Acid. Angew. Chem. Int. Ed. 2015, 54, 647-650.
  • Zhao, Z.-L.; Gu, Q.; Wu, X.-Y.*; You, S.-L.* Pd(0)-catalyzed benzylation of indole through η3-benzyl palladium intermediate. Chin. J. Catal. 2015, 36, 15-18.

Year 2014

Posted in 2014 on 十二月 9th, 2013 by Delta – 评论关闭
  • Zheng, C.*; Zhuo, C.-X.; You, S.-L.* Mechanistic Insights into the Pd-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Multisubstituted Pyrroles: Understanding the Remarkable Regio- and Enantioselectivity. J. Am. Chem. Soc. 2014, 136, 16251-16259.
  • Zheng, J.; You, S.-L.* Construction of Axial Chirality by Rhodium-Catalyzed Asymmetric Dehydrogenative Heck Coupling of Biaryl Compounds with Alkenes. Angew. Chem. Int. Ed. 2014, 53, 13244-13247.
  • Xu, R.-Q.; Gu, Q.; Wu, W.-T.; Zhao, Z.-A.; You, S.-L.* Construction of Erythrinane Skeleton via Pd(0)-Catalyzed Intramolecular Dearomatization of para-Aminophenols. J. Am. Chem. Soc. 2014, 136, 15469-15472.
  • Ye, K.-Y.; Zhang, X.; Dai, L.-X.; You, S.-L.* Ruthenium-Catalyzed Regioselective Allylic Trifluoromethylthiolation Reaction. J. Org. Chem. 2014, 79, 12106-12110.
  • Yang, Z.-P.; Zhang, W.; You, S.-L.* Catalytic Asymmetric Reactions by Metal and Chiral Phosphoric Acid Sequential Catalysis. J. Org. Chem. 2014, 79, 7785-7798.
  • Gao, D.-W.; Gu, Q.*; You, S.-L.* Pd(II)-Catalyzed Intermolecular Direct C–H Bond Iodination: An Efficient Approach toward the Synthesis of Axially Chiral Compounds via Kinetic Resolution. ACS Catal. 2014, 4, 2741-2745.
  • Gao, R.-D.; Liu, C.; Dai, L.-X.; Zhang, W.; You, S.-L.* Pd(0)-Catalyzed Alkenylation and Allylic Dearomatization Reactions between Nucleophile-Bearing Indoles and Propargyl Carbonate. Org. Lett. 2014, 16, 3919–3921.
  • Duan, D.-H.; Yin, Q.; Wang, S.-G.; You, S.-L.* Chiral Phosphoric Acid-Catalyzed Asymmetric Cascade Reaction of C(3) Substituted Indoles and Methyl Vinyl Ketone. Acta Chim. Sinica 2014, 72, 1001-1004.
  • Zhuo, C.-X.; Zheng, C.; You, S.-L.* Transition-Metal-Catalyzed Asymmetric Allylic Dearomatization Reactions. Acc. Chem. Res. 2014, 47, 2558-2573.
  • Zheng, J.; You, S.-L.* Rhodium-catalyzed direct coupling of biaryl pyridine derivatives with internal alkynes. Chem. Commun. 2014, 50, 8204-8207.
  • Liu, H.; Zheng, C.*; You, S.-L.* Fe(OTf)3 Catalyzed Annulation of 2,3-Disubstituted Indoles with Aziridines. Chin. J. Chem. 2014, 709-714.
  • Lai, Z.-W.; Yang, R.-F.; Ye, K.-Y.; Sun, H.*; You, S.-L.* Synthesis of 1-[bis(trifluoromethyl)phosphine]-1’-oxazolinylferrocene ligands and their application in regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates. Beilstein J. Org. Chem. 2014, 10, 1261-1266.
  • Yang, Z.-P.; Wu, Q.-F.; You, S.-L.* Direct Asymmetric Dearomatization of Pyridines and Pyrazines by Iridium-Catalyzed Allylic Amination Reactions. Angew. Chem. Int. Ed. 2014, 53, 6986-6989.
  • Zhuo, C.-X.; You, S.-L.* Palladium-Catalyzed Intermolecular Allylic Dearomatization Reaction of α-Substituted β-Naphthol Derivatives: Scope and Mechanistic Investigation. Adv. Synth. Catal. 2014, 356, 2020-2028.
  • Zhuo, C.-X.; Zhou, Y.; You, S.-L.* Highly Regio- and Enantioselective Synthesis of Poly-Substituted 2H-Pyrroles via Pd-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Pyrroles. J. Am. Chem. Soc. 2014, 136, 6590-6593.
  • Yang, Z.-P.; Zhuo, C.-X.; You, S.-L.* Ruthenium-Catalyzed Intramolecular Allylic Dearomatization/Migration Reaction of Indoles and Pyrroles. Adv. Synth. Catal. 2014, 356, 1731-1734.
  • Liu, C.; Zhang, W.; Dai, L.-X.; You, S.-L.* Copper-Catalyzed C-2 Arylation or Vinylation of Indole Derivatives with Iodonium Salts. Chem. Asian J. 2014, 9, 2113-2118.
  • Yin, Q.; You, S.-L.* Asymmetric Chlorocyclization of Indole-3-yl-benzamides for the Construction of Fused Indolines. Org. Lett. 2014, 16, 2426-2429.
  • Gao, D.-W.; Yin, Q.; Gu, Q.*; You, S.-L.* Enantioselective Synthesis of Planar Chiral Ferrocenes via Pd(0)-Catalyzed Intramolecular Direct C-H Bond Arylation. J. Am. Chem. Soc. 2014, 136, 4841-4844.
  • Yin, Q.; You, S.-L.* Asymmetric Chlorination/Ring Expansion for the Synthesis of α-Quaternary Cycloalkanones. Org. Lett. 2014, 16, 1810-1813.
  • Ye, K.-Y.; Dai, L.-X.; You, S.-L.* Regio- and Enantioselective Synthesis of N-Allylindoles by Iridium-Catalyzed Allylic Tmination/Transition-Metal-Catalyzed Cyclization Reactions. Chem. Eur. J. 2014, 20, 3040-3044.
  • Zhao, Q.; Zhuo, C.-X.; You, S.-L.* Enantioselective synthesis of N-allylindoles via palladium-catalyzed allylic amination/oxidation of indolines. RSC Adv. 2014, 4, 10875-10878.
  • Li, W.; Liu, C.; Zhang, H.; Ye, K.; Zhang, G.; Zhang, W.; Duan, Z.; You, S.*; Lei, A.* Palladium-Catalyzed Oxidative Carbonylation ofN-Allylamines for the Synthesis of beta-Lactams. Angew. Chem. Int. Ed. 2014, 53, 2443-2446.
  • Wang, S.-G.; You, S.-L.* Hydrogenative Dearomatization of Pyridine and Asymmetric Aza-Friedel–Crafts Alkylation Sequence. Angew. Chem. Int. Ed. 2014, 53, 2194-2197.
  • Liu, H.; Zheng, C.*; You, S.-L.* Catalytic C6 Functionalization of 2,3-Disubstituted Indoles by Scandium Triflate. J. Org. Chem. 2014, 79, 1047-1054.
  • Zheng, C.; You, S.-L.* Recent development of direct asymmetric functionalization of inert C–H bonds. RSC Adv. 2014, 4, 6173-6214.
  • Shi, Y.-C.; Wang, S.-G.; Yin, Q.; You, S.-L.* N-alkylation of indole via ring-closing metathesis/isomerization/Mannich cascade under ruthenium/chiral phosphoric acid sequential catalysis. Org. Chem. Front. 2014, 1, 39-43.
  • Han, L.; Liu, C.; Zhang, W.; Shi, X.-X.; You, S.-L.* Dearomatization of Tryptophols via a Vanadium-Catalyzed Asymmetric Epoxidation and Ring-Opening Cascade. Chem. Commun. 2014, 50, 1231-1233.
  • Zhang, X.; Han, L.; You, S.-L.* Ir-Catalyzed Intermolecular Asymmetric Allylic Dearomatization Reaction of Indoles. Chem. Sci. 2014, 5, 1059-1063.
  • Cai, Q.; Yin, Q.; You, S.-L.* Chiral-Amine-Catalyzed Asymmetric Bromocyclization of Tryptamine Derivatives. Asian J. Org. Chem. 2014, 3, 408-411.

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.

Year 2012

Posted in 2012 on 十一月 23rd, 2011 by Delta – 评论关闭
  • Zhuo, C.-X.; Zhang, W.*; You, S.-L.* Catalytic Asymmetric Dearomatization Reactions. Angew. Chem. Int. Ed. 2012, 51, 12662-12686.
  • Jia, M.-Q.; Liu, C.; You, S.-L.* Diastereoselective and Enantioselective Desymmetrization of α-Substituted Cyclohexadienones via Intramolecular Stetter Reaction. J. Org. Chem. 2012, 77, 10996-11001.
  • Zeng, M.; Zhang, W.; You, S.-L.* One-Pot Synthesis of Pyrrolo[1,2-a]indoles by Chiral N-Triflyl Phosphoramide Catalyzed Friedel-Crafts Alkylation of 4,7-Dihydroindole with β,γ-Unsaturated α-Keto Esters. Chin. J. Chem. 2012, 30, 2615-2623.
  • Cai, Q.; Liang, X.-W.; Wang, S.-G.; Zhang, J.-W.; Zhang, X.; You, S.-L.* Ring-Closing Metathesis/Isomerization/Pictet–Spengler Cascade via Ruthenium/Chiral Phosphoric Acid Sequential Catalysis. Org. Lett. 2012, 14, 5022-5025.
  • Cai, Q.; Liu, C.; Liang, X.-W.; You, S.-L.* Enantioselective Construction of Pyrroloindolines via Chiral Phosphoric Acid Catalyzed Cascade Michael Addition–Cyclization of Tryptamines. Org. Lett. 2012, 14, 4588-4590.
  • Liu, C.; Zhang, W.; Dai, L.-X.; You, S.-L.* Copper(I)-Catalyzed Cascade Dearomatization of 2-Substituted Tryptophols with Arylidonium Salts. Org. Lett. 2012, 14, 4525-4527.
  • Wu, K.-J.; Dai, L.-X.; You, S.-L.* Palladium(0)-Catalyzed Dearomative Arylation of Indoles: Convenient Access to Spiroindolenine Derivatives. Org. Lett. 2012, 14, 3772-3775.
  • Liu, C.; Zhang, W.; Dai, L.-X.; You, S.-L.* Cascade Dearomatization of N-Subsituted Tryptophols via Lewis Acid-Catalyzed Michael Reaction. Org. Biomol. Chem. 2012, 10, 7177-7183.
  • Xu, Q.-L.; Dai, L.-X.; You, S.-L.* Iridium-Catalyzed Enantioselective Allylic Alkylation of Methyl 2-(4-nitrophenylsulfonyl)acetate and Subsequent Transformations. Adv. Synth. Catal. 2012, 354, 2275-2282.
  • Yin, Q.; You, S.-L.* Intramolecular Alkene Electrophilic Bromination Initiated ipso-Bromocyclization for the Synthesis of Functionalized Azaspirocyclohexadienones. Org. Lett. 2012, 14, 3526-3529.
  • Cai, Q.; You, S.-L.* Organocatalyzed Enantioselective Formal [4 + 2] Cycloaddition of 2,3-Disubstituted Indole and Methyl Vinyl Ketone. Org. Lett. 2012, 14, 3040-3043.
  • Jia, M.-Q.; You, S.-L.* Desymmetrization of Cyclohexadienones via D-Camphor-derived Triazolium Salts Catalyzed Intramolecular Stetter Reaction. Chem. Commun. 2012, 48, 6363-6365.
  • Xu, Q.-L.; Dai, L.-X.; You, S.-L.* Enantioselective Synthesis of Tetrahydroisoquinolines via Iridium-Catalyzed Intramolecular Friedel–Crafts-Type Allylic Alkylation of Phenols. Org. Lett. 2012, 2579-2581.
  • He, H.; Ye, K.-Y.; Wu, Q.-F.; Dai, L.-X.; You, S.-L.* Iridium-Catalyzed Asymmetric Allylic Etherification and Ring-Closing Metathesis Reaction for Enantioselective Synthesis of Chromene and 2,5-Dihydrobenzo[b]oxepine Derivatives. Adv. Synth. Catal. 2012, 354, 1084-1094.
  • Liu, W.-B.; Zhang, X.; Dai, L.-X.; You, S.-L.* Asymmetric N-Allylation of Indoles Through the Iridium-Catalyzed Allylic Alkylation/Oxidation of Indolines. Angew. Chem. Int. Ed. 2012, 51, 5183-5187.
  • Zhang, J.-W.; Xu, Z.; Gu, Q.; Shi, X.-X.; Leng, X.-B.; You, S.-L.* Chiral counteranion-directed silver-catalyzed asymmetric synthesis of 1,2-dihydroisoquinolines by FriedeleCrafts alkylation reactions. Tetrahedron 2012, 68, 5263-5268.
  • Ye, K.-Y.; Dai, L.-X.; You, S.-L.* Enantioselective synthesis of 2,5-dihydrobenzo[b]azepine derivatives via iridium-catalyzed asymmetric allylic amination with 2-allylanilines and ring-closing-metathesis reaction. Org. Biomol. Chem. 2012, 5932-5939.
  • Wang, S.-G.; Han, L.; Zeng, M.; Sun, F.-L.; Zhang, W.; You, S.-L.* Enantioselective synthesis of fluorene derivatives by chiral N-triflyl phosphoramide catalyzed double Friedel–Crafts alkylation reaction. Org. Biomol. Chem. 2012, 10, 3202-3209.
  • Liu, W.-B.; Zheng, C.; Zhuo, C.-X.; Dai, L.-X.; You, S.-L.* Ir-Catalyzed Allylic Alkylation Reaction with N-Aryl Phosphoramidite Ligands: Scope and Mechanistic Studies. J. Am. Chem. Soc. 2012, 134, 4812-4821.
  • Zheng, C.; You, S.-L.* Transfer hydrogenation with Hantzsch esters and related organic hydride donors. Chem. Soc. Rev. 2012, 41, 2498-2518.
  • Wu, Q.-F.; Zheng, C.; You, S.-L.* Enantioselective Synthesis of Spiro Cyclopentane-1,3′-indoles and 2,3,4,9-Tetrahydro-1H-carbazoles by Iridium-Catalyzed Allylic Dearomatization and Stereospecific Migration. Angew. Chem. Int. Ed. 2012, 51, 1680-1683.
  • Zhuo, C.-X.; Liu, W.-B.; Wu, Q.-F.; You, S.-L.* Asymmetric dearomatization of pyrroles via Ir-catalyzed allylic substitution reaction: enantioselective synthesis of spiro-2H-pyrroles. Chem. Sci. 2012, 3,  205-208.

Year 2011

Posted in 2011 on 十二月 16th, 2010 by Delta – 评论关闭
  • Rong, Z.-Q.; Jia, M.-Q.; You, S.-L.* (1R,2R)-DPEN-derived triazolium salts for enantioselective oxodiene Diels–Alder reactions. Tetrahedron 2011, 67, 9329-9333.
  • Ye, K.-Y.; He, H.; Liu, W.-B.; Dai, L.-X.; Helmchen, G.; You, S.-L.* Iridium-Catalyzed Allylic Vinylation and Asymmetric Allylic Amination Reactions with ortho-Aminostyrenes. J. Am. Chem. Soc. 2011, 133, 19006-19014.
  • Gu, Q.; You, S.-L.* Desymmetrization of Cyclohexadienones via Asymmetric Michael Reaction Catalyzed by Cinchonine-Derived Urea. Org. Lett. 2011, 13, 5192-5195.
  • Cai, Q.; Zheng, C.; Zhang, J.-W.; You, S.-L.* Enantioselective Michael/Mannich Polycyclization Cascade of Indolyl Enones Catalyzed by Quinine-Derived Primary Amines. Angew. Chem. Int. Ed. 2011, 50, 8665-8669.
  • Rong, Z.-Q.; Jia, M.-Q.; You, S.-L.* Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to α,β-Unsaturated Aldehydes by Redox Oxidation. Org. Lett. 2011, 13, 4080-4083.
  • Gu, Q.; You, S.-L.* Desymmetrization of cyclohexadienones via cinchonine derived thiourea-catalyzed enantioselective aza-Michael reaction and total synthesis of (-)-Mesembrine. Chem. Sci. 2011, 2, 1519-1522.
  • Yin, Q.; You, S.-L.* Chiral phosphoric acid-catalysed Friedel–Crafts alkylation reaction of indoles with racemic spiro indolin-3-ones. Chem. Sci. 2011, 2, 1344-1348.
  • Wu, Q.-F.; Liu, W.-B.; Zhuo, C.-X.; Rong, Z.-Q.; Ye, K.-Y.; You, S.-L.* Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization of Phenols. Angew. Chem. Int. Ed. 2011, 50, 4455-4458.
  • Su, H.; Xie, Y.,* Liu, W.-B.; You, S.-L.* Methyl-monofluorination of Ibuprofen Selectively Increases Its Inhibitory Activity toward Cyclooxygenase-1 Leading to Enhanced Analgesic Activity and Reduced Gastric Damage In Vivo. Bioorg. Med. Chem. Lett. 2011, 21, 3578-3582.
  • Zhang, J.-W.; Cai, Q.; Shi, X.-X.; Zhang, W.; You, S.-L.* Enantioselective Synthesis of Tetrahydropyrano[3,4-b] Indoles Catalyzed by Chiral N-Triflyl Phosphoramide via Intramolecular Friedel-Crafts Alkylation Reaction. Synlett 2011, 1239-1242. (Invited Cluster “Brønsted Acid Catalysis”)
  • Rong, Z.-Q.; Li, Y.; Yang, G.-Q.; You, S.-L.* D-Camphor-derived Triazolium Salts for Enantioselective Intramolecular Stetter Reactions. Synlett 2011, 1033-1037. (Invited special issue for Professor Xiyan Lu and Professor Li-Xin Dai)
  • Rong, Z.-Q.; Zhang, W.; Yang, G.-Q.*; You, S.-L.* N-Heterocyclic Carbene-Catalyzed Redox Reactions of α-Functionalized Aldehydes. Curr. Org. Chem. 2011, 15, 3077-3090.
  • Jia, M.-Q.; Li, Y.; Rong, Z.-Q.; You, S.-L.* Synthesis of (1R,2R)-DPEN-Derived Triazolium Salts and Their Application in Asymmetric Intramolecular Stetter Reactions. Org. Biomol. Chem. 2011, 9, 2072-2074. (submission by invitation)
  • Wu, K.-J.; Li, G.-Q.; Li, Y.; Dai, L.-X.; You, S.-L.* N-Heterocyclic Carbene-Catalyzed Tandem Aza-Benzoin/Michael Reactions: On Site Reversal of the Reactivity of N-Boc Imines. Chem. Commun. 2011, 47, 493-495. (Emerging Investigators Themed Issue)

Book Chapters

Posted in Book Chapters on 六月 7th, 2010 by Delta – 评论关闭
  • Chao Zheng, Shu-Li You, “Reduction: Asymmetric Transfer Hydrogenation with Hantzsch Esters”. In Erick M. Carreira, Hisashi Yamamoto (eds.) Comprehensive Chirality, Volume 6, pp. 586-607. Amsterdam: Elsevier.
  • Wen-Bo Liu, Ji-Bao Xia, Shu-Li You, “Iridium-Catalyzed Asymmetric Allylic Substitutions”, Top Organomet Chem, Springer-Verlag Berlin Heidelberg 2012, 38, 155-208.
  • Shu-Li You, Ji-Bao Xia, “Palladium-Catalyzed Aryl–Aryl Bond Formation Through Double C–H Activation”, Top Curr Chem, Springer-Verlag Berlin Heidelberg 2010, 292, 165-194.
  • Shu-Li You, Chapter 8 “Unsymmetrical 1,1’-Bidentate Ferrocenyl Ligands”. In: Li-Xin Dai, Xue-Long Hou (eds.) Chiral Ferrocene Ligands in Asymmetric Catalysis, pp. 215-256. Wiley-VCH, 2010.
  • Ji-Bao Xia, Timothy F. Jamison, Shu-Li You, Chapter 3 “Monodentate Chiral Ferrocenyl Ligands”. In: Li-Xin Dai, Xue-Long Hou (eds.) Chiral Ferrocene Ligands in Asymmetric Catalysis, pp. 55-71. Wiley-VCH, 2010.
  • Shu-Li You, 3.2 “Addition to Carbonyl Compounds-Imines”. In: Marco Bandini, Achille Umani-Ronchi (eds.) Catalytic Asymmetric Friedel-Crafts Alkylations. Wiley-VCH, 2009.
  • 游书力,李毅,“新型反应介质”,p270,《10000个科学难题》,北京:科学出版社, 2009
  • 游书力,郑晓建,康强,第11章“组合酸催化剂在不对称催化中的应用”,丁奎岭,范青华主编,《不对称催化新概念与新方法》,化学工业出版社, 2008

Before 2006

Posted in Before on 六月 7th, 2010 by Delta – 评论关闭
  • You, S.-L.; Kelly, J. W. Total synthesis of didmolamides A&B. Tetrahedron Lett. 2005, 46, 2567-2570.
  • You, S.-L.; Kelly, J. W. The total synthesis of Bistratamides F-I. Tetrahedron 2005, 61, 241-249.
  • Songpon, D.; Powers, E. T.; You, S.-L.; Kelly, J. W. Controlling the morphology of cross β–sheet assemblies by rational design. J. Am. Chem. Soc. 2005, 127, 8562-8570.
  • Hou, X.-L.; You, S.-L.; Tao, T.; Deng, W.-P.; Wu, X.-W.; Li, M.; Yuan, K.; Dai, L.-X. Enantioselective transition-metal catalyzed carbon-carbon bond formation reactions using novel chiral ferrocenes and cyclophanes. Top. in Catalysis 2005, 35, 87-103.
  • You, S.-L.; Kelly, J. W. Total synthesis of dendroamide A: oxazole and thiazole construction using an oxodiphosphonium salt. J. Org. Chem. 2003, 68, 9506-9609.
  • You, S.-L.; Kelly, J. W. Highly efficient biomimetic total synthesis and structural verification of bistratamides E and J from lissoclinum bistratum. Chem. Eur. J. 2004, 10, 71-75.
  • You, S.-L.; Songpon, D.; Kelly, J. W. Solid-phase synthesis and stereochemical assignments of tenuecyclamides A-D employing heterocyclic amino acids derived from commercially available Fmoc α-amino acids. Org. Lett. 2004, 6, 2627-2630.
  • You, S.-L.; Kelly, J. W. Highly efficient enantiospecific synthesis of imidazoline-containing amino acids using bis(triphenyl)oxodiphosphonium trifluoromethanesulfonate. Org. Lett. 2004, 6, 1681-1683.
  • Songpon, D.; You, S.-L.; Kelly, J. W. Synthesis of all nineteen appropriately protected chiral α-hydroxy acid equivalents of the α-amino acids for Boc solid-phase depsi-peptide synthesis. Org. Lett. 2004, 6, 497-500.
  • You, S.-L.; Hou, X.-L.; Dai, L.-X. Application of chiral ferrocene ligands in asymmetric palladium catalyzed allylic substitution reactions J. Graduate School of the Chinese Academy of Sciences 2004, 21, 413.
  • You, S.-L.; Razavi, H.; Kelly, J. W. A biomimetic synthesis of thiazolines using hexaphenyl- oxodiphosphonium trifluoromethanesulfonate. Angew. Chem. Int. Ed. 2003, 42, 83-85.
  • Dai, L.-X.; Tu, T.; You, S.-L.; Deng, W.-P.; Hou, X.-L. Asymmetric catalysis with chiral ferrocene ligands. Acc. Chem. Res. 2003, 36, 659-667.
  • You, S.-L.; Hou, X.-L.; Dai, L.-X.; Yu, Y.-H.; Xia, W.  Role of planar chirality of S, N- and P, N-ferrocene ligands in palladium-catalyzed allylic substitutions. J. Org. Chem. 2002, 67, 4684-4695.
  • You, S.-L.; Hou, X.-L.; Dai, L.-X.; Zhu, X.-Z. Highly efficient ligands for palladium-catalyzed asymmetric alkylation of ketone enolates. Org. Lett. 2001, 3, 149-151.
  • You, S.-L.; Zhu, X.-Z.; Luo, Y.-M.; Hou, X.-L.; Dai, L.-X. Highly regio- and enantioselective Pd-catalyzed allylic alkylation and amination of monosubstituted allylic acetates with novel ferrocene P,N-ligands. J. Am. Chem. Soc. 2001, 123, 7471-7472.
  • Deng, W.-P.; You, S.-L.; Hou, X.-L.; Dai, L.-X.; Yu, Y.-H.; Xia, W.; Sun, J. Importance of planar chirality in chiral catalysts with three chiral elements: the role of planar chirality in 2′-substituted-1,1′-P,N-ferrocene ligands on the enantioselectivity in Pd-catalyzed allylic substitution. J. Am. Chem. Soc. 2001, 123, 6508-6519.
  • You, S.-L.; Zhu, X.-Z.; Hou, X.-L.; Dai, L.-X. Synthesis of new diphosphine ligands and their applications in palladium-catalyzed allylic alkylation to construct chiral quaternary carbon center. Huaxue Xuebao 2001, 59, 1667-1674.
  • You, S.-L.; Luo, Y.-M.; Deng, W.-P.; Hou, X.-L.; Dai, L.-X. Palladium-catalyzed asymmetric allylic alkylations of cycloalkenyl acetates with planar chiral phosphino-ferrocene carboxylic acids. J. Organometallic Chem. 2001, 637-639, 845-849.
  • You, S.-L.; Hou, X.-L.; Dai, L.-X. Novel ferrocene modified P,N-ligands for enantioselective palladium-catalyzed allylic substitution reactions. J. Organometallic Chem. 2001, 637-639, 762-766.
  • You, S.-L.; Hou, X.-L.; Dai, L.-X. Synthesis of planar chiral selenide derivatives of ferrocenyl-oxazoline and their application in enantioselective palladium catalyzed allylic substitution reaction. Tetrahedron: Asymmetry 2000, 11, 1495-1500.
  • You, S.-L.; Hou, X.-L.; Dai, L.-X.; Cao, B.-X.; Sun, J. Novel bis-N-[2-(diphenylphosphino)- ferrocenylcarbonyl]diaminocyclohexane ligands: application in asymmetric allylic alkylation of imino esters with simple allyl carbonate. Chem. Commun. 2000, 1933-1934.
  • Dai, L.-X.; Hou, X.-L.; Deng, W.-P.; You, S.-L.; Zhou, Y.-G. The application of ligands with planar chirality in asymmetric synthesis. Pure Appl. Chem. 1999, 71, 1401-1405.
  • You, S.-L.; Zhou, Y.-G.; Hou, X.-L.; Dai, L.-X. Enantioselective palladium catalyzed allylic substitution with chiral thioether derivatives of ferrocenyl-oxazoline and the role of planar chirality in this reaction. Chem. Commun. 1998, 2765-2766.

Year 2006

Posted in 2006 on 六月 7th, 2010 by Delta – 评论关闭
  • You, S.-L.*; Dai, L.-X. Enantioselective Palladium-Catalyzed Decarboxylative Allylic Alkylations. Angew. Chem. Int. Ed. 2006, 45, 5246-5248.