메뉴 건너뛰기




Volumn 48, Issue 7, 2015, Pages 1832-1844

Asymmetric Catalytic Cascade Reactions for Constructing Diverse Scaffolds and Complex Molecules

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL PRODUCT; CYCLOBUTANE DERIVATIVE; INDOLE DERIVATIVE; PIPERIDINE; PIPERIDINE DERIVATIVE;

EID: 84937431669     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/acs.accounts.5b00217     Document Type: Article
Times cited : (293)

References (53)
  • 2
    • 0026418434 scopus 로고
    • The Atom Economy - A Search for Synthetic Efficiency
    • Trost, B. M. The Atom Economy-A Search for Synthetic Efficiency Science 1991, 254, 1471-1477
    • (1991) Science , vol.254 , pp. 1471-1477
    • Trost, B.M.1
  • 3
    • 38949138457 scopus 로고    scopus 로고
    • Function Oriented Synthesis, Step Economy, and Drug Design
    • Wender, P. A.; Verma, V. A.; Paxton, T. J.; Pillow, T. H. Function Oriented Synthesis, Step Economy, and Drug Design Acc. Chem. Res. 2008, 41, 40-49
    • (2008) Acc. Chem. Res. , vol.41 , pp. 40-49
    • Wender, P.A.1    Verma, V.A.2    Paxton, T.J.3    Pillow, T.H.4
  • 5
    • 34347335758 scopus 로고    scopus 로고
    • Strategies To Bypass the Taxol Problem. Enantioselective Cascade Catalysis, a New Approach for the Efficient Construction of Molecular Complexity
    • Walji, A. M.; MacMillan, D. W. C. Strategies To Bypass the Taxol Problem. Enantioselective Cascade Catalysis, a New Approach for the Efficient Construction of Molecular Complexity Synlett 2007, 1477-1489
    • (2007) Synlett , pp. 1477-1489
    • Walji, A.M.1    MacMillan, D.W.C.2
  • 6
    • 67650984682 scopus 로고    scopus 로고
    • Protecting-Group-Free Synthesis as an Opportunity for Invention
    • Young, I. S.; Baran, P. S. Protecting-Group-Free Synthesis as an Opportunity for Invention Nat. Chem. 2009, 1, 193-205
    • (2009) Nat. Chem. , vol.1 , pp. 193-205
    • Young, I.S.1    Baran, P.S.2
  • 8
    • 34247109045 scopus 로고    scopus 로고
    • Natural Products as Sources of New Drugs over the Last 25 Years
    • Newman, D. J.; Cragg, G. M. Natural Products as Sources of New Drugs over the Last 25 Years J. Nat. Prod. 2007, 70, 461-477
    • (2007) J. Nat. Prod. , vol.70 , pp. 461-477
    • Newman, D.J.1    Cragg, G.M.2
  • 9
    • 0000908715 scopus 로고
    • Enantioselective Methods for Chiral Cyclohexane Ring Synthesis
    • Schultz, A. G. Enantioselective Methods for Chiral Cyclohexane Ring Synthesis Acc. Chem. Res. 1990, 23, 207-213
    • (1990) Acc. Chem. Res. , vol.23 , pp. 207-213
    • Schultz, A.G.1
  • 10
    • 70349095283 scopus 로고    scopus 로고
    • Synthetic Approaches to the Neuraminidase Inhibitors Zanamivir (Relenza) and Oseltamivir Phosphate (Tamiflu) for the Treatment of Influenza
    • Magano, J. Synthetic Approaches to the Neuraminidase Inhibitors Zanamivir (Relenza) and Oseltamivir Phosphate (Tamiflu) for the Treatment of Influenza Chem. Rev. 2009, 109, 4398-4438
    • (2009) Chem. Rev. , vol.109 , pp. 4398-4438
    • Magano, J.1
  • 13
    • 72449151738 scopus 로고    scopus 로고
    • Asymmetric Organocatalytic Relay Cascades: Catalyst-Controlled Stereoisomer Selection in the Synthesis of Functionalized Cyclohexanes
    • Wang, Y.; Han, R.-G.; Zhao, Y.-L.; Yang, S.; Xu, P.-F.; Dixon, D. J. Asymmetric Organocatalytic Relay Cascades: Catalyst-Controlled Stereoisomer Selection in the Synthesis of Functionalized Cyclohexanes Angew. Chem., Int. Ed. 2009, 48, 9834-9838
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 9834-9838
    • Wang, Y.1    Han, R.-G.2    Zhao, Y.-L.3    Yang, S.4    Xu, P.-F.5    Dixon, D.J.6
  • 15
    • 14844285469 scopus 로고    scopus 로고
    • Amaryllidaceae and Sceletium Alkaloids
    • Jin, Z. Amaryllidaceae and Sceletium Alkaloids Nat. Prod. Rep. 2005, 22, 111-126
    • (2005) Nat. Prod. Rep. , vol.22 , pp. 111-126
    • Jin, Z.1
  • 16
    • 34547216418 scopus 로고    scopus 로고
    • Amaryllidaceae and Sceletium Alkaloids
    • Jin, Z. Amaryllidaceae and Sceletium Alkaloids Nat. Prod. Rep. 2007, 24, 886-905
    • (2007) Nat. Prod. Rep. , vol.24 , pp. 886-905
    • Jin, Z.1
  • 17
    • 84867250820 scopus 로고    scopus 로고
    • Concise Construction of the Tetracyclic Core of Lycorine-Type Alkaloids and the Formal Synthesis of α-Lycorane Based on Asymmetric Bifunctional Thiourea-Catalyzed Cascade Reaction
    • Wang, Y.; Luo, Y. C.; Zhang, H. B.; Xu, P. F. Concise Construction of the Tetracyclic Core of Lycorine-Type Alkaloids and the Formal Synthesis of α-Lycorane Based on Asymmetric Bifunctional Thiourea-Catalyzed Cascade Reaction Org. Biomol. Chem. 2012, 10, 8211-8215
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 8211-8215
    • Wang, Y.1    Luo, Y.C.2    Zhang, H.B.3    Xu, P.F.4
  • 18
    • 36749025633 scopus 로고    scopus 로고
    • Pyrrolidinylspirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents
    • Galliford, C. V.; Scheidt, K. A. Pyrrolidinylspirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents Angew. Chem., Int. Ed. 2007, 46, 8748-8758
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 8748-8758
    • Galliford, C.V.1    Scheidt, K.A.2
  • 19
    • 84898873012 scopus 로고    scopus 로고
    • Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis
    • Narayan, R.; Potowski, M.; Jia, Z.-J.; Antonchick, A. P.; Waldmann, H. Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis Acc. Chem. Res. 2014, 47, 1296-1310
    • (2014) Acc. Chem. Res. , vol.47 , pp. 1296-1310
    • Narayan, R.1    Potowski, M.2    Jia, Z.-J.3    Antonchick, A.P.4    Waldmann, H.5
  • 20
    • 84880648097 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Multicomponent Cascade Reaction via 1,3-Proton Shift and [3 + 2] Cycloaddition: An Efficient Strategy for the Synthesis of Oxindole Derivatives
    • Tian, L.; Hu, X.-Q.; Li, Y.-H.; Xu, P.-F. Organocatalytic Asymmetric Multicomponent Cascade Reaction via 1,3-Proton Shift and [3 + 2] Cycloaddition: An Efficient Strategy for the Synthesis of Oxindole Derivatives Chem. Commun. 2013, 49, 7213-7215
    • (2013) Chem. Commun. , vol.49 , pp. 7213-7215
    • Tian, L.1    Hu, X.-Q.2    Li, Y.-H.3    Xu, P.-F.4
  • 22
    • 84896786583 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies
    • Cheng, D.; Ishihara, Y.; Tan, B.; Barbas, C. F., III. Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies ACS Catal. 2014, 4, 743-762
    • (2014) ACS Catal. , vol.4 , pp. 743-762
    • Cheng, D.1    Ishihara, Y.2    Tan, B.3    Barbas, C.F.4
  • 23
    • 84896916606 scopus 로고    scopus 로고
    • Hydrogen-Bond-Directed Formal [5 + 1] Annulations of Oxindoles with Ester-Linked Bisenones: Facile Access to Chiral Spirooxindole δ-Lactones
    • Zhao, S.; Lin, J.-B.; Zhao, Y.-Y.; Liang, Y.-M.; Xu, P.-F. Hydrogen-Bond-Directed Formal [5 + 1] Annulations of Oxindoles with Ester-Linked Bisenones: Facile Access to Chiral Spirooxindole δ-Lactones Org. Lett. 2014, 16, 1802-1805
    • (2014) Org. Lett. , vol.16 , pp. 1802-1805
    • Zhao, S.1    Lin, J.-B.2    Zhao, Y.-Y.3    Liang, Y.-M.4    Xu, P.-F.5
  • 24
    • 84881242218 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Synthesis of Tetracyclic Pyridocarbazole Derivatives by Using a Diels-Alder/Aza-Michael/Aldol Condensation Domino Reaction
    • Enders, D.; Joie, C.; Deckers, H. Organocatalytic Asymmetric Synthesis of Tetracyclic Pyridocarbazole Derivatives by Using a Diels-Alder/Aza-Michael/Aldol Condensation Domino Reaction Chem.-Eur. J. 2013, 19, 10818-10821
    • (2013) Chem. - Eur. J. , vol.19 , pp. 10818-10821
    • Enders, D.1    Joie, C.2    Deckers, H.3
  • 25
    • 78149438715 scopus 로고    scopus 로고
    • Enantioselective Intramolecular Aza-Michael Additions of Indoles Catalyzed by Chiral Phosphoric Acids
    • Cai, Q.; Zheng, C.; You, S.-L. Enantioselective Intramolecular Aza-Michael Additions of Indoles Catalyzed by Chiral Phosphoric Acids Angew. Chem., Int. Ed. 2010, 49, 8666-8669
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 8666-8669
    • Cai, Q.1    Zheng, C.2    You, S.-L.3
  • 26
    • 84867324818 scopus 로고    scopus 로고
    • Recent Advances in Organocatalytic Methods for the Synthesis of Disubstituted 2- and 3-Indolinones
    • Dalpozzo, R.; Bartoli, G.; Bencivenni, G. Recent Advances in Organocatalytic Methods for the Synthesis of Disubstituted 2- and 3-Indolinones Chem. Soc. Rev. 2012, 41, 7247-7290
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 7247-7290
    • Dalpozzo, R.1    Bartoli, G.2    Bencivenni, G.3
  • 27
    • 84899788924 scopus 로고    scopus 로고
    • Organocatalytic Asymmetric Michael-Michael Cascade for the Construction of Highly Functionalized N-Fused Piperidinoindoline Derivatives
    • Zhao, Y.-L.; Wang, Y.; Cao, J.; Liang, Y.-M.; Xu, P.-F. Organocatalytic Asymmetric Michael-Michael Cascade for the Construction of Highly Functionalized N-Fused Piperidinoindoline Derivatives Org. Lett. 2014, 16, 2438-2441
    • (2014) Org. Lett. , vol.16 , pp. 2438-2441
    • Zhao, Y.-L.1    Wang, Y.2    Cao, J.3    Liang, Y.-M.4    Xu, P.-F.5
  • 29
    • 84876323185 scopus 로고    scopus 로고
    • Progress in Asymmetric Organocatalyzed Michael Addition/Hemi-aminoacetalization/Acylimminium-Cyclization Cascade Reactions
    • Chen, J.; Liu, Q.; Dai, X.; Nie, L.; Fang, H.; Wu, X. Progress in Asymmetric Organocatalyzed Michael Addition/Hemi-aminoacetalization/Acylimminium-Cyclization Cascade Reactions Chin. J. Org. Chem. 2013, 33, 1-17
    • (2013) Chin. J. Org. Chem. , vol.33 , pp. 1-17
    • Chen, J.1    Liu, Q.2    Dai, X.3    Nie, L.4    Fang, H.5    Wu, X.6
  • 30
    • 84866104518 scopus 로고    scopus 로고
    • α-Oxo-γ-butyrolactam, N-Containing Pronucleophile in Organocatalytic One-Pot Assembly of Butyrolactam-Fused Indoloquinolizidines
    • Zhu, H.-L.; Ling, J.-B.; Xu, P.-F. α-Oxo-γ-butyrolactam, N-Containing Pronucleophile in Organocatalytic One-Pot Assembly of Butyrolactam-Fused Indoloquinolizidines J. Org. Chem. 2012, 77, 7737-7743
    • (2012) J. Org. Chem. , vol.77 , pp. 7737-7743
    • Zhu, H.-L.1    Ling, J.-B.2    Xu, P.-F.3
  • 31
    • 84906946049 scopus 로고    scopus 로고
    • One-Pot Asymmetric Synthesis of Quaternary Pyrroloindolones through a Multicatalytic N-Allylation/Hydroacylation Sequence
    • Lu, H.; Lin, J.-B.; Liu, J.-Y.; Xu, P.-F. One-Pot Asymmetric Synthesis of Quaternary Pyrroloindolones through a Multicatalytic N-Allylation/Hydroacylation Sequence Chem.-Eur. J. 2014, 20, 11659-11663
    • (2014) Chem. - Eur. J. , vol.20 , pp. 11659-11663
    • Lu, H.1    Lin, J.-B.2    Liu, J.-Y.3    Xu, P.-F.4
  • 32
    • 33646071885 scopus 로고    scopus 로고
    • Hydroacylation of Activated Ketones Catalyzed by N-Heterocyclic Carbenes
    • Chan, A.; Scheidt, K. A. Hydroacylation of Activated Ketones Catalyzed by N-Heterocyclic Carbenes J. Am. Chem. Soc. 2006, 128, 4558-4559
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4558-4559
    • Chan, A.1    Scheidt, K.A.2
  • 33
    • 84859747983 scopus 로고    scopus 로고
    • Organocatalytic Umpolung: N-Heterocyclic Carbenes and Beyond
    • Bugaut, X.; Glorius, F. Organocatalytic Umpolung: N-Heterocyclic Carbenes and Beyond Chem. Soc. Rev. 2012, 41, 3511-3522
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 3511-3522
    • Bugaut, X.1    Glorius, F.2
  • 34
    • 84875799416 scopus 로고    scopus 로고
    • Acyl Anion Free N-Heterocyclic Carbene Organocatalysis
    • Ryan, S. J.; Candish, L.; Lupton, D. W. Acyl Anion Free N-Heterocyclic Carbene Organocatalysis Chem. Soc. Rev. 2013, 42, 4906-4917
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 4906-4917
    • Ryan, S.J.1    Candish, L.2    Lupton, D.W.3
  • 35
    • 84894254223 scopus 로고    scopus 로고
    • On the Mechanism of N-Heterocyclic Carbene-Catalyzed Reactions Involving Acyl Azoliums
    • Mahatthananchai, J.; Bode, J. W. On the Mechanism of N-Heterocyclic Carbene-Catalyzed Reactions Involving Acyl Azoliums Acc. Chem. Res. 2014, 47, 696-707
    • (2014) Acc. Chem. Res. , vol.47 , pp. 696-707
    • Mahatthananchai, J.1    Bode, J.W.2
  • 39
    • 53849146010 scopus 로고    scopus 로고
    • Proline-Mediated Enantioselective Construction of Tetrahydropyridines via a Cascade Mannich-Type/Intramolecular Cyclization Reaction
    • Han, R.-G.; Wang, Y.; Li, Y.-Y.; Xu, P.-F. Proline-Mediated Enantioselective Construction of Tetrahydropyridines via a Cascade Mannich-Type/Intramolecular Cyclization Reaction Adv. Synth. Catal. 2008, 350, 1474-1478
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1474-1478
    • Han, R.-G.1    Wang, Y.2    Li, Y.-Y.3    Xu, P.-F.4
  • 40
    • 77950257271 scopus 로고    scopus 로고
    • Multiple-Organocatalyst-Promoted Cascade Reaction: A Fast and Efficient Entry into Fully Substituted Piperidines
    • Wang, Y.; Yu, D.-F.; Liu, Y.-Z.; Wei, H.; Luo, Y.-C.; Dixon, D. J.; Xu, P.-F. Multiple-Organocatalyst-Promoted Cascade Reaction: A Fast and Efficient Entry into Fully Substituted Piperidines Chem.-Eur. J. 2010, 16, 3922-3925
    • (2010) Chem. - Eur. J. , vol.16 , pp. 3922-3925
    • Wang, Y.1    Yu, D.-F.2    Liu, Y.-Z.3    Wei, H.4    Luo, Y.-C.5    Dixon, D.J.6    Xu, P.-F.7
  • 41
    • 77957824693 scopus 로고    scopus 로고
    • Enantio- and Diastereoselective Synthesis of Piperidines by Coupling of Four Components in a "One-Pot" Sequence Involving Diphenylprolinol Silyl Ether Mediated Michael Reaction
    • Urushima, T.; Sakamoto, D.; Ishikawa, H.; Hayashi, Y. Enantio- and Diastereoselective Synthesis of Piperidines by Coupling of Four Components in a "One-Pot" Sequence Involving Diphenylprolinol Silyl Ether Mediated Michael Reaction Org. Lett. 2010, 12, 4588-4591
    • (2010) Org. Lett. , vol.12 , pp. 4588-4591
    • Urushima, T.1    Sakamoto, D.2    Ishikawa, H.3    Hayashi, Y.4
  • 42
    • 78449308247 scopus 로고    scopus 로고
    • One-Pot Enantioselective Syntheses of Iminosugar Derivatives Using Organocatalytic Anti-Michael-Anti-Aza-Henry Reactions
    • Imashiro, R.; Uehara, H.; Barbas, C. F., III. One-Pot Enantioselective Syntheses of Iminosugar Derivatives Using Organocatalytic Anti-Michael-Anti-Aza-Henry Reactions Org. Lett. 2010, 12, 5250-5253
    • (2010) Org. Lett. , vol.12 , pp. 5250-5253
    • Imashiro, R.1    Uehara, H.2    Barbas, C.F.3
  • 43
    • 79954416883 scopus 로고    scopus 로고
    • Organocatalytic Enantioselective Multicomponent Cascade Reaction: Facile Access to Tetrahydropyridines with C3 All-Carbon Quaternary Stereocenters
    • Yu, D.-F.; Wang, Y.; Xu, P.-F. Organocatalytic Enantioselective Multicomponent Cascade Reaction: Facile Access to Tetrahydropyridines with C3 All-Carbon Quaternary Stereocenters Tetrahedron 2011, 67, 3273-3277
    • (2011) Tetrahedron , vol.67 , pp. 3273-3277
    • Yu, D.-F.1    Wang, Y.2    Xu, P.-F.3
  • 44
    • 0003593745 scopus 로고
    • Ed. The Chemistry of Heterocyclic Compounds, Vol. Wiley: New York
    • Chromenes, Chromanones, and Chromones; Ellis, G. P., Ed.; The Chemistry of Heterocyclic Compounds, Vol. 31; Wiley: New York, 1977.
    • (1977) Chromenes, Chromanones, and Chromones , vol.31
    • Ellis, G.P.1
  • 45
    • 84880009151 scopus 로고    scopus 로고
    • Organocatalyzed Michael-Michael Cascade Reaction: Asymmetric Synthesis of Polysubstituted Chromans
    • Jia, Z.-X; Luo, Y.-C; Cheng, X.-N.; Xu, P.-F.; Gu, Y.-C. Organocatalyzed Michael-Michael Cascade Reaction: Asymmetric Synthesis of Polysubstituted Chromans J. Org. Chem. 2013, 78, 6488-6494
    • (2013) J. Org. Chem. , vol.78 , pp. 6488-6494
    • Jia, Z.-X.1    Luo, Y.-C.2    Cheng, X.-N.3    Xu, P.-F.4    Gu, Y.-C.5
  • 46
    • 81555226814 scopus 로고    scopus 로고
    • Diastereo- and Enantioselective Synthesis of a Novel Tetracyclic Ring System via an Organocatalytic One-Pot Reaction
    • Yu, D. F.; Wang, Y.; Xu, P. F. Diastereo- and Enantioselective Synthesis of a Novel Tetracyclic Ring System via an Organocatalytic One-Pot Reaction Adv. Synth. Catal. 2011, 353, 2960-2965
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 2960-2965
    • Yu, D.F.1    Wang, Y.2    Xu, P.F.3
  • 47
    • 84893836958 scopus 로고    scopus 로고
    • An Efficient Strategy for the Synthesis of Polysubstituted Chromeno[4,3- b ]pyrrolidine Derivatives
    • Tian, L.; Xu, G.-Q.; Li, Y.-H.; Liang, Y.-M.; Xu, P.-F. An Efficient Strategy for the Synthesis of Polysubstituted Chromeno[4,3- b ]pyrrolidine Derivatives Chem. Commun. 2014, 50, 2428-2430
    • (2014) Chem. Commun. , vol.50 , pp. 2428-2430
    • Tian, L.1    Xu, G.-Q.2    Li, Y.-H.3    Liang, Y.-M.4    Xu, P.-F.5
  • 48
    • 80755126169 scopus 로고    scopus 로고
    • Advances in the Chemistry of Tetrahydroquinolines
    • Sridharan, V.; Suryavanshi, P. A.; Menéndez, J. C. Advances in the Chemistry of Tetrahydroquinolines Chem. Rev. 2011, 111, 7157-7259
    • (2011) Chem. Rev. , vol.111 , pp. 7157-7259
    • Sridharan, V.1    Suryavanshi, P.A.2    Menéndez, J.C.3
  • 49
    • 79952147389 scopus 로고    scopus 로고
    • Highly Enantioselective Synthesis of Polysubstituted Tetrahydroquinolines via Organocatalytic Michael/Aza-Henry Tandem Reactions
    • Jia, Z.-X.; Luo, Y.-C.; Xu, P.-F. Highly Enantioselective Synthesis of Polysubstituted Tetrahydroquinolines via Organocatalytic Michael/Aza-Henry Tandem Reactions Org. Lett. 2011, 13, 832-835
    • (2011) Org. Lett. , vol.13 , pp. 832-835
    • Jia, Z.-X.1    Luo, Y.-C.2    Xu, P.-F.3
  • 50
    • 84867049980 scopus 로고    scopus 로고
    • Organocatalytic Aza-Michael-Michael Cascade Reactions: A Flexible Approach to 2,3,4-Trisubstituted Tetrahydroquinolines
    • Jia, Z.-X.; Luo, Y.-C.; Wang, Y.; Chen, L.; Xu, P.-F.; Wang, B.-H. Organocatalytic Aza-Michael-Michael Cascade Reactions: A Flexible Approach to 2,3,4-Trisubstituted Tetrahydroquinolines Chem.-Eur. J. 2012, 18, 12958-12961
    • (2012) Chem. - Eur. J. , vol.18 , pp. 12958-12961
    • Jia, Z.-X.1    Luo, Y.-C.2    Wang, Y.3    Chen, L.4    Xu, P.-F.5    Wang, B.-H.6
  • 51
    • 84876914569 scopus 로고    scopus 로고
    • Organocatalytic Formal [2 + 2] Cycloaddition Initiated by Vinylogous Friedel-Crafts Alkylation: Enantioselective Synthesis of Substituted Cyclobutane Derivatives
    • Duan, G.-J.; Ling, J.-B.; Wang, W.-P.; Luo, Y.-C.; Xu, P.-F. Organocatalytic Formal [2 + 2] Cycloaddition Initiated by Vinylogous Friedel-Crafts Alkylation: Enantioselective Synthesis of Substituted Cyclobutane Derivatives Chem. Commun. 2013, 49, 4625-4627
    • (2013) Chem. Commun. , vol.49 , pp. 4625-4627
    • Duan, G.-J.1    Ling, J.-B.2    Wang, W.-P.3    Luo, Y.-C.4    Xu, P.-F.5
  • 52
    • 84863115170 scopus 로고    scopus 로고
    • Hydrogen-Bond-Mediated Cascade Reaction Involving Chalcones: Facile Synthesis of Enantioenriched Trisubstituted Tetrahydrothiophenes
    • Ling, J.-B.; Su, Y.; Zhu, H.-L.; Wang, G.-Y.; Xu, P.-F. Hydrogen-Bond-Mediated Cascade Reaction Involving Chalcones: Facile Synthesis of Enantioenriched Trisubstituted Tetrahydrothiophenes Org. Lett. 2012, 14, 1090-1093
    • (2012) Org. Lett. , vol.14 , pp. 1090-1093
    • Ling, J.-B.1    Su, Y.2    Zhu, H.-L.3    Wang, G.-Y.4    Xu, P.-F.5
  • 53
    • 84887083597 scopus 로고    scopus 로고
    • Organocatalytic Cascade Sulfa-Michael/Aldol Reaction of β,β-Disubstituted Enones: Enantioselective Synthesis of Tetrahydrothiophenes with a Trifluoromethylated Quaternary Center
    • Su, Y.; Ling, J.-B.; Zhang, S.; Xu, P.-F. Organocatalytic Cascade Sulfa-Michael/Aldol Reaction of β,β-Disubstituted Enones: Enantioselective Synthesis of Tetrahydrothiophenes with a Trifluoromethylated Quaternary Center J. Org. Chem. 2013, 78, 11053-11058
    • (2013) J. Org. Chem. , vol.78 , pp. 11053-11058
    • Su, Y.1    Ling, J.-B.2    Zhang, S.3    Xu, P.-F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.