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Volumn 41, Issue 8, 2008, Pages 937-948

Ylide-initiated michael addition-cyclization reactions beyond cyclopropanes

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Indexed keywords


EID: 51649105642     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar800108z     Document Type: Article
Times cited : (374)

References (58)
  • 1
    • 4143093678 scopus 로고    scopus 로고
    • Catalytic Asymmetric Sulfur Ylide-Mediated Epoxidation of Carbonyl Compounds: Scope, Selectivity, and Applications in Synthesis
    • For a review on catalytic ylide cyclizatio via a metal carbene route, see:a
    • For a review on catalytic ylide cyclizatio via a metal carbene route, see:(a) Aggarwal, V. K.; Winn, C. L. Catalytic Asymmetric Sulfur Ylide-Mediated Epoxidation of Carbonyl Compounds: Scope, Selectivity, and Applications in Synthesis. Acc. Chem. Res. 2004, 37, 611-620.
    • (2004) Acc. Chem. Res , vol.37 , pp. 611-620
    • Aggarwal, V.K.1    Winn, C.L.2
  • 2
    • 0034619269 scopus 로고    scopus 로고
    • Selected examples: (b) Aggarwal, V. K.; Smith, H. W.; Hynd, G.; Jones, R. V. H.; Fieldhouse, R.; Spey, S. E. Catalytic Cyclopropanation of Electron Deficient Alkenes Mediated by Chiral and Achiral Sulfides: Scope and Limitations in Reactions Involving Phenyldiazomethane and Ethyl Diazoacetate. J. Chem. Soc., Perkin Trans. 1 2000, 3267-3276.
    • Selected examples: (b) Aggarwal, V. K.; Smith, H. W.; Hynd, G.; Jones, R. V. H.; Fieldhouse, R.; Spey, S. E. Catalytic Cyclopropanation of Electron Deficient Alkenes Mediated by Chiral and Achiral Sulfides: Scope and Limitations in Reactions Involving Phenyldiazomethane and Ethyl Diazoacetate. J. Chem. Soc., Perkin Trans. 1 2000, 3267-3276.
  • 3
    • 0035901642 scopus 로고    scopus 로고
    • Application of Chiral Sulfides to Catalytic Asymmetric Aziridination and Cyclopropanation with in Situ Generation of the Diazo Compound
    • (c) Aggarwal, V. K.; Alonso, E.; Fang, G.; Ferrara, M.; Hynd, G.; Porcelloni, M. Application of Chiral Sulfides to Catalytic Asymmetric Aziridination and Cyclopropanation with in Situ Generation of the Diazo Compound. Angew Chem., Int. Ed. 2001, 40, 1433-1436.
    • (2001) Angew Chem., Int. Ed , vol.40 , pp. 1433-1436
    • Aggarwal, V.K.1    Alonso, E.2    Fang, G.3    Ferrara, M.4    Hynd, G.5    Porcelloni, M.6
  • 4
    • 29544442212 scopus 로고    scopus 로고
    • Asymmetric Sulfonium Ylide Mediated Cyclopropanation: Stereocontrolled Synthesis of (+)-LY354740
    • (d) Aggarwal, V. K.; Grange, E. Asymmetric Sulfonium Ylide Mediated Cyclopropanation: Stereocontrolled Synthesis of (+)-LY354740. Chem. - Eur. J. 2006, 12, 568-575.
    • (2006) Chem. - Eur. J , vol.12 , pp. 568-575
    • Aggarwal, V.K.1    Grange, E.2
  • 5
    • 20544465347 scopus 로고    scopus 로고
    • The First Example of Catalytic Aziridination Mediated by Arsonium Ylides: Preparation of trans-Pentafluorophenyl-Containing Aziridines
    • (e) Zhu, S.-F.; Liao, Y.; Zhu, S.-Z. The First Example of Catalytic Aziridination Mediated by Arsonium Ylides: Preparation of trans-Pentafluorophenyl-Containing Aziridines. Synlett 2005, 1429-1432.
    • (2005) Synlett , pp. 1429-1432
    • Zhu, S.-F.1    Liao, Y.2    Zhu, S.-Z.3
  • 6
    • 4544374715 scopus 로고    scopus 로고
    • An Intramolecular Organocatalytic Cyclopropanation Reaction
    • For selected recent examples on organocatalytic ylide cyclization, see:a
    • For selected recent examples on organocatalytic ylide cyclization, see:(a) Bremeyer, N.; Smith, S. C.; Ley, S. V.; Gaunt, M. J. An Intramolecular Organocatalytic Cyclopropanation Reaction. Angew. Chem., Int. Ed. 2004, 43, 2681-2684.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 2681-2684
    • Bremeyer, N.1    Smith, S.C.2    Ley, S.V.3    Gaunt, M.J.4
  • 7
    • 5344280509 scopus 로고    scopus 로고
    • Enantioselective Organocatalytic Cyclopropanation via Ammonium Ylides
    • (b) Papageorgiou, C. D.; de Dios, M. A. C.; Ley, S. V.; Gaunt, M. J. Enantioselective Organocatalytic Cyclopropanation via Ammonium Ylides. Angew. Chem., Int. Ed. 2004, 43, 4641-4644.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 4641-4644
    • Papageorgiou, C.D.1    de Dios, M.A.C.2    Ley, S.V.3    Gaunt, M.J.4
  • 8
    • 33748765777 scopus 로고    scopus 로고
    • Enantioselective Catalytic Intramolecular Cyclopropanation Using Modified Cinchona Alkaloid Organocatalysts
    • (c) Johansson, C. C. C.; Bremeyer, N.; Ley, S. V.; Owen, D. R.; Smith, S. C.; Gaunt, M. J. Enantioselective Catalytic Intramolecular Cyclopropanation Using Modified Cinchona Alkaloid Organocatalysts. Angew. Chem., Int. Ed. 2006, 45, 6024-6028.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 6024-6028
    • Johansson, C.C.C.1    Bremeyer, N.2    Ley, S.V.3    Owen, D.R.4    Smith, S.C.5    Gaunt, M.J.6
  • 9
    • 14944346768 scopus 로고    scopus 로고
    • Enantioselective Organocatalytic Cyclopropanations. The Identification of a New Class of Iminium Catalyst Based upon Directed Electrostatic Activation
    • (d) Kunz, R. K.; MacMillan, D. W. C. Enantioselective Organocatalytic Cyclopropanations. The Identification of a New Class of Iminium Catalyst Based upon Directed Electrostatic Activation. J. Am. Chem. Soc. 2005, 127, 3240-3241.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 3240-3241
    • Kunz, R.K.1    MacMillan, D.W.C.2
  • 10
    • 0000171402 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Three-membered ring Compounds via Ylide Routes
    • For reviews, see:a
    • For reviews, see:(a) Dai, L.-X.; Hou, X.-L.; Zhou, Y.-G. Stereoselective Synthesis of Three-membered ring Compounds via Ylide Routes. Pure Appl. Chem. 1999, 71, 369-376.
    • (1999) Pure Appl. Chem , vol.71 , pp. 369-376
    • Dai, L.-X.1    Hou, X.-L.2    Zhou, Y.-G.3
  • 11
    • 0001485086 scopus 로고    scopus 로고
    • Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement
    • (b) Li, A.-H.; Dai, L.-X.; Aggarwal, V. K. Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement. Chem. Rev. 1997, 97, 2341-2372.
    • (1997) Chem. Rev , vol.97 , pp. 2341-2372
    • Li, A.-H.1    Dai, L.-X.2    Aggarwal, V.K.3
  • 13
    • 38349102427 scopus 로고    scopus 로고
    • Recent Developments in the Use of Catalytic Asymmetric Ammonium Enolates in Chemical Synthesis
    • (d) Gaunt, M. J.; Johansson, C. C. C. Recent Developments in the Use of Catalytic Asymmetric Ammonium Enolates in Chemical Synthesis. Chem. Rev. 2007, 107, 5596-5605.
    • (2007) Chem. Rev , vol.107 , pp. 5596-5605
    • Gaunt, M.J.1    Johansson, C.C.C.2
  • 15
    • 84985559736 scopus 로고
    • Synthetic Applications of Sulphonium Salts and Sulphonium Ylides
    • Stirling, C. J. M, Patai, S, Eds, Wiley:New York
    • Block, E. Synthetic Applications of Sulphonium Salts and Sulphonium Ylides. In The Chemistry of the Sulphonium Group; Stirling, C. J. M., Patai, S., Eds.; Wiley:New York, 1981; pp 673-702.
    • (1981) The Chemistry of the Sulphonium Group , pp. 673-702
    • Block, E.1
  • 16
    • 0000786896 scopus 로고
    • A New Synthesis of α,β-Unsaturated Carboxylic Esters Using Dialkyltelluronium Carbethoxymethylide
    • Osuka, A.; Mori, Y.; Shimizu, H.; Suzuki, H. A New Synthesis of α,β-Unsaturated Carboxylic Esters Using Dialkyltelluronium Carbethoxymethylide. Tetrahedron Lett. 1983, 24, 2599-2602.
    • (1983) Tetrahedron Lett , vol.24 , pp. 2599-2602
    • Osuka, A.1    Mori, Y.2    Shimizu, H.3    Suzuki, H.4
  • 17
    • 0342960175 scopus 로고
    • Michael Addition of Silylated Telluronium Allylide to α,β-Unsaturated Esters: Facile and Stereoselective Synthesis of Trimethylsilylvinylcyclopropane Derivatives
    • Huang, Y.-Z.; Tang, Y.; Zhou, Z.-L.; Huang, J.-L. Michael Addition of Silylated Telluronium Allylide to α,β-Unsaturated Esters: Facile and Stereoselective Synthesis of Trimethylsilylvinylcyclopropane Derivatives. J. Chem. Soc., Chem. Commun. 1993, 7-9.
    • (1993) J. Chem. Soc., Chem. Commun , pp. 7-9
    • Huang, Y.-Z.1    Tang, Y.2    Zhou, Z.-L.3    Huang, J.-L.4
  • 18
    • 0001597125 scopus 로고    scopus 로고
    • Cyclopropanation Reactions of Allylic Ylides with α,β-Unsaturated Esters and Amides: Tuning of Stereoselectivity and the Dramatic Effect of Lithium Salts
    • Tang, Y.; Huang, Y. Z.; Dai, L.-X.; Sun, J.; Xia, W. Cyclopropanation Reactions of Allylic Ylides with α,β-Unsaturated Esters and Amides: Tuning of Stereoselectivity and the Dramatic Effect of Lithium Salts. J. Org. Chem. 1996, 61, 5762-5769.
    • (1996) J. Org. Chem , vol.61 , pp. 5762-5769
    • Tang, Y.1    Huang, Y.Z.2    Dai, L.-X.3    Sun, J.4    Xia, W.5
  • 19
    • 0034703419 scopus 로고    scopus 로고
    • Switching of Stereoselectivity: Dramatic Effects of HMPA on the Stereoselectiviy of Cyclopropanation Reaction of Silylated Tellronium Allylide with α,β-Unsaturated Esters and Amides
    • (a) Ye, S.; Tang, Y.; Dai, L. X. Switching of Stereoselectivity: Dramatic Effects of HMPA on the Stereoselectiviy of Cyclopropanation Reaction of Silylated Tellronium Allylide with α,β-Unsaturated Esters and Amides. J. Org. Chem. 2000, 65, 6257-6260.
    • (2000) J. Org. Chem , vol.65 , pp. 6257-6260
    • Ye, S.1    Tang, Y.2    Dai, L.X.3
  • 20
    • 27844449972 scopus 로고    scopus 로고
    • Tang, Y.; Ye, S.; Sun, X.-L. Telluronium and Sulfonium Ylides for Organic Transformation. Synlett 2005, 2720-2730.
    • (b) Tang, Y.; Ye, S.; Sun, X.-L. Telluronium and Sulfonium Ylides for Organic Transformation. Synlett 2005, 2720-2730.
  • 21
    • 0001004410 scopus 로고    scopus 로고
    • An Efficient Stereocontrolled Strategy in the Cyclopropanation Reactions of α,β-Unsaturated Ketones with Semistabilized Ylides; Highly Selective Synthesis of Two Geometrical Isomers of Vinyl-substituted Cyclopropane Derivatives
    • Tang, Y.; Huang, Y.-Z.; Dai, L.-X.; Sun, J.; Xia, W. An Efficient Stereocontrolled Strategy in the Cyclopropanation Reactions of α,β-Unsaturated Ketones with Semistabilized Ylides; Highly Selective Synthesis of Two Geometrical Isomers of Vinyl-substituted Cyclopropane Derivatives. J. Org. Chem. 1997, 62, 954-959.
    • (1997) J. Org. Chem , vol.62 , pp. 954-959
    • Tang, Y.1    Huang, Y.-Z.2    Dai, L.-X.3    Sun, J.4    Xia, W.5
  • 22
    • 0000100584 scopus 로고    scopus 로고
    • Recent Advances in Asymmetric Catalytic Metal Carbene Transformations
    • Doyle, M. P.; Forbes, D. C. Recent Advances in Asymmetric Catalytic Metal Carbene Transformations. Chem. Rev. 1998, 98, 911-936.
    • (1998) Chem. Rev , vol.98 , pp. 911-936
    • Doyle, M.P.1    Forbes, D.C.2
  • 23
    • 0033970914 scopus 로고    scopus 로고
    • Cheng, D.; Knox, K. R.; Cohen, T. Tandem Lithium-ene Cyclization and Thiophenoxide Expulsion to Produce Fused Vinylcyclopropanes: First Observation of Allylic Lithium Oxyanion-induced Reactivity and Stereoselectivity in Intramolecular Carbolithiation. J. Am. Chem. Soc. 2000, 122, 412-413.
    • (a) Cheng, D.; Knox, K. R.; Cohen, T. Tandem Lithium-ene Cyclization and Thiophenoxide Expulsion to Produce Fused Vinylcyclopropanes: First Observation of Allylic Lithium Oxyanion-induced Reactivity and Stereoselectivity in Intramolecular Carbolithiation. J. Am. Chem. Soc. 2000, 122, 412-413.
  • 24
    • 0000244357 scopus 로고    scopus 로고
    • Reverse of Regioselectivity in Intramolecular Nucleophilic Substitution of μ-Allyl Palladium Species. Highly Selective Formation of Vinylic Cyclopropanes via the Pd(0)-catalyzed Coupling-cyclization Reaction of Organic Iodides with 2-(2′,3′-Dienyl)malonates
    • (b) Ma, S.; Zhao, S. Reverse of Regioselectivity in Intramolecular Nucleophilic Substitution of μ-Allyl Palladium Species. Highly Selective Formation of Vinylic Cyclopropanes via the Pd(0)-catalyzed Coupling-cyclization Reaction of Organic Iodides with 2-(2′,3′-Dienyl)malonates. Org. Lett. 2000, 2, 2495-2497.
    • (2000) Org. Lett , vol.2 , pp. 2495-2497
    • Ma, S.1    Zhao, S.2
  • 25
    • 0142214626 scopus 로고    scopus 로고
    • Controllable Diastereoselective Cyclopropanation. Enantioselective Synthesis of Vinylcyclopropanes via Chiral Telluronium Ylides
    • Liao, W.-W.; Li, K.; Tang, Y. Controllable Diastereoselective Cyclopropanation. Enantioselective Synthesis of Vinylcyclopropanes via Chiral Telluronium Ylides. J. Am. Chem. Soc. 2003, 125, 13030-13031.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 13030-13031
    • Liao, W.-W.1    Li, K.2    Tang, Y.3
  • 26
    • 51649105789 scopus 로고    scopus 로고
    • Ph D thesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences
    • Liao, W.-W. Stereoselective Ylide Cyclopropanation and Aziridination, Ph D thesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 2004, pp 5-66.
    • (2004) Stereoselective Ylide Cyclopropanation and Aziridination , pp. 5-66
    • Liao, W.-W.1
  • 27
    • 0037139547 scopus 로고    scopus 로고
    • A Novel Chiral Sulfonium Yilde: Highly Enantioselective Synthesis of Vinylcyclopropanes
    • Ye, S.; Huang, Z.-Z.; Xia, C.-A.; Tang, Y.; Dai, L.-X. A Novel Chiral Sulfonium Yilde: Highly Enantioselective Synthesis of Vinylcyclopropanes. J. Am. Chem. Soc. 2002, 124, 2432-2433.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 2432-2433
    • Ye, S.1    Huang, Z.-Z.2    Xia, C.-A.3    Tang, Y.4    Dai, L.-X.5
  • 28
    • 0030024622 scopus 로고    scopus 로고
    • For the preparation of sulfide 12, see: Li, A.-H.; Dai, L.-X.; Hou, X.-L.; Huang, Y.-Z.; Li, F.-W. Preparation of Enantiomerically Enriched (2R,3R)- or (2S,3S)-trans-2,3-Diaryloxiranes via Camphor-Derived Sulfonium Ylides. J. Org. Chem. 1996, 61, 489-493.
    • For the preparation of sulfide 12, see: Li, A.-H.; Dai, L.-X.; Hou, X.-L.; Huang, Y.-Z.; Li, F.-W. Preparation of Enantiomerically Enriched (2R,3R)- or (2S,3S)-trans-2,3-Diaryloxiranes via Camphor-Derived Sulfonium Ylides. J. Org. Chem. 1996, 61, 489-493.
  • 29
    • 33746630913 scopus 로고    scopus 로고
    • Enantioselective Synthesis of Vinylcyclopropanes and Vinylepoxides Mediated by Camphor-Derived Sulfur Ylides: Rationale of Enantioselectivity, Scope, and Limitation
    • Deng, X.-M.; Cai, P.; Ye, S.; Sun, X.-L.; Liao, W.-W.; Li, K.; Tang, Y.; Wu, Y.-D.; Dai, L.-X. Enantioselective Synthesis of Vinylcyclopropanes and Vinylepoxides Mediated by Camphor-Derived Sulfur Ylides: Rationale of Enantioselectivity, Scope, and Limitation. J. Am. Chem. Soc. 2006, 128, 9730-9740.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 9730-9740
    • Deng, X.-M.1    Cai, P.2    Ye, S.3    Sun, X.-L.4    Liao, W.-W.5    Li, K.6    Tang, Y.7    Wu, Y.-D.8    Dai, L.-X.9
  • 30
    • 0037629473 scopus 로고
    • A Facile Synthesis of α,β-Unsaturated Epoxides via Diisobutylallyltelluronium Bromide
    • Zhou, Z.-L.; Sun, Y.-S.; Shi, L.-L.; Huang, Y.-Z. A Facile Synthesis of α,β-Unsaturated Epoxides via Diisobutylallyltelluronium Bromide. J. Chem. Soc., Chem. Commun. 1990, 1439-1440.
    • (1990) J. Chem. Soc., Chem. Commun , pp. 1439-1440
    • Zhou, Z.-L.1    Sun, Y.-S.2    Shi, L.-L.3    Huang, Y.-Z.4
  • 31
    • 24644463157 scopus 로고    scopus 로고
    • The Michael Addition-Elimination of Ylides to α,β-Unsaturated Imines. Highly Stereoselective Synthesis of Vinylcyclopropanecarbaldehydes and Vinylcyclopropylaziridines
    • Zheng, J.-C.; Liao, W.-W.; Tang, Y.; Sun, X.-L.; Dai, L.-X. The Michael Addition-Elimination of Ylides to α,β-Unsaturated Imines. Highly Stereoselective Synthesis of Vinylcyclopropanecarbaldehydes and Vinylcyclopropylaziridines. J. Am. Chem. Soc. 2005, 127, 12222-12223.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 12222-12223
    • Zheng, J.-C.1    Liao, W.-W.2    Tang, Y.3    Sun, X.-L.4    Dai, L.-X.5
  • 32
    • 0029905332 scopus 로고    scopus 로고
    • Highly Stereoselective Synthesis of Vinyl and Ethynylcyclopropane 1,1-Dicarboxylic Esters via Semi-stabilized Telluronium Ylides
    • Tang, Y.; Chi, Z.-F.; Huang, Y.-Z.; Dai, L.-X.; Yu, Y.-H. Highly Stereoselective Synthesis of Vinyl and Ethynylcyclopropane 1,1-Dicarboxylic Esters via Semi-stabilized Telluronium Ylides. Tetrahedron 1996, 8747-8757.
    • (1996) Tetrahedron , pp. 8747-8757
    • Tang, Y.1    Chi, Z.-F.2    Huang, Y.-Z.3    Dai, L.-X.4    Yu, Y.-H.5
  • 33
    • 0037884930 scopus 로고    scopus 로고
    • Donor-Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis
    • Reissig, H.-U.; Zimmer, R. Donor-Acceptor-Substituted Cyclopropane Derivatives and Their Application in Organic Synthesis. Chem. Rev. 2003, 103, 1151-1196.
    • (2003) Chem. Rev , vol.103 , pp. 1151-1196
    • Reissig, H.-U.1    Zimmer, R.2
  • 34
    • 28044450399 scopus 로고    scopus 로고
    • Highly Stereoselective Synthesis of Trisubstituted Vinylcyclopropane Derivatives via Arsonium Ylides
    • Jiang, H.; Deng, X.-M.; Sun, X.-L.; Tang, Y.; Dai, L.-X. Highly Stereoselective Synthesis of Trisubstituted Vinylcyclopropane Derivatives via Arsonium Ylides. J. Org. Chem. 2005, 70, 10202-10205.
    • (2005) J. Org. Chem , vol.70 , pp. 10202-10205
    • Jiang, H.1    Deng, X.-M.2    Sun, X.-L.3    Tang, Y.4    Dai, L.-X.5
  • 35
    • 42749083542 scopus 로고    scopus 로고
    • 3-catalyzed Ylide Cyclopropanation for the Synthesis of Trisubstituted Vinylcyclopropane Derivatives
    • 3-catalyzed Ylide Cyclopropanation for the Synthesis of Trisubstituted Vinylcyclopropane Derivatives. Tetrahedron 2008, 64, 5032-5035.
    • (2008) Tetrahedron , vol.64 , pp. 5032-5035
    • Jiang, H.1    Sun, X.-L.2    Zhu, C.-Y.3    Dai, L.-X.4    Tang, Y.5
  • 36
    • 33947337893 scopus 로고
    • Cyclopropanes from Reactions of Ethyl Dimethylsulfuranylideneacetate with α,β-Unsaturated Compounds
    • Payne, G. B. Cyclopropanes from Reactions of Ethyl Dimethylsulfuranylideneacetate with α,β-Unsaturated Compounds. J. Org. Chem. 1967, 32, 3351-3355.
    • (1967) J. Org. Chem , vol.32 , pp. 3351-3355
    • Payne, G.B.1
  • 37
    • 51549085809 scopus 로고    scopus 로고
    • Highly Diastereoselective and Enantioselective Formal [4 + 1] Ylide Annulation for the Synthesis of Optically Active Dihydrofurans
    • in press
    • Zheng, J.-C.; Zhu, C.-Y.; Sun, X.-L.; Tang, Y.; and Dai, L.-X. Highly Diastereoselective and Enantioselective Formal [4 + 1] Ylide Annulation for the Synthesis of Optically Active Dihydrofurans. J. Org. Chem.,in press.
    • J. Org. Chem
    • Zheng, J.-C.1    Zhu, C.-Y.2    Sun, X.-L.3    Tang, Y.4    Dai, L.-X.5
  • 40
    • 43049102341 scopus 로고    scopus 로고
    • Synthesis of Isoxazoline N-oxides and Its Application in the Formal Synthesis of Dehydroclausenamide
    • (a) Zhu, C.-Y.; Sun, X.-L.; Deng, X.-M.; Zheng, J.-C.; Tang, Y. Synthesis of Isoxazoline N-oxides and Its Application in the Formal Synthesis of Dehydroclausenamide. Tetrahedron 2008, 64, 5583-5589.
    • (2008) Tetrahedron , vol.64 , pp. 5583-5589
    • Zhu, C.-Y.1    Sun, X.-L.2    Deng, X.-M.3    Zheng, J.-C.4    Tang, Y.5
  • 41
    • 0344010056 scopus 로고    scopus 로고
    • Concise Total Synthesis of (-)-Dehydroclausenamide Utilizing the Novel Formation of cis-Epoxide as the Key Step
    • (b) Yan, Z.; Wang, J.; Tian, W. A. Concise Total Synthesis of (-)-Dehydroclausenamide Utilizing the Novel Formation of cis-Epoxide as the Key Step. Tetrahedron Lett. 2003, 44, 9383-9384.
    • (2003) Tetrahedron Lett , vol.44 , pp. 9383-9384
    • Yan, Z.1    Wang, J.2    Tian, W.A.3
  • 42
    • 33847652883 scopus 로고    scopus 로고
    • Tandem and Domino Catalytic Strategies for Enantioselective Synthesis
    • (a) Chapman, C. J.; Frost, C. G. Tandem and Domino Catalytic Strategies for Enantioselective Synthesis. Synthesis 2007, 1-21.
    • (2007) Synthesis , pp. 1-21
    • Chapman, C.J.1    Frost, C.G.2
  • 44
    • 30444443444 scopus 로고    scopus 로고
    • Catalytic Asymmetric Tandem Transformations Triggered by Conjugate Additions
    • (c) Guo, H.; Ma, J. Catalytic Asymmetric Tandem Transformations Triggered by Conjugate Additions. Angew. Chem., Int. Ed. 2006, 45, 354-366.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 354-366
    • Guo, H.1    Ma, J.2
  • 45
    • 34250701681 scopus 로고    scopus 로고
    • The Synthesis of Chromenes, Chromanes, Coumarins and Related Heterocycles via Tandem Reactions of Salicylic Aldehydes or Salicylic Imines with α,β-Unsaturated Compounds
    • and references cited therein. For recent review, see
    • For recent review, see:Shi, Y.-L.; Shi, M. The Synthesis of Chromenes, Chromanes, Coumarins and Related Heterocycles via Tandem Reactions of Salicylic Aldehydes or Salicylic Imines with α,β-Unsaturated Compounds. Org. Biomol. Chem. 2007, 5, 1499-1504, and references cited therein.
    • (2007) Org. Biomol. Chem , vol.5 , pp. 1499-1504
    • Shi, Y.-L.1    Shi, M.2
  • 46
    • 33748600681 scopus 로고    scopus 로고
    • An Unexpected Tandem Ylide Annulation Reaction for Controllable Synthesis of 2H-Chromenes and 4H-Chromenes
    • Ye, L.-W.; Sun, X.-L.; Zhu, C.-Y.; Tang, Y. An Unexpected Tandem Ylide Annulation Reaction for Controllable Synthesis of 2H-Chromenes and 4H-Chromenes. Org. Lett. 2006, 8, 3853-3856.
    • (2006) Org. Lett , vol.8 , pp. 3853-3856
    • Ye, L.-W.1    Sun, X.-L.2    Zhu, C.-Y.3    Tang, Y.4
  • 47
    • 33847002748 scopus 로고    scopus 로고
    • Tetrahydrothiophene-Catalyzed Synthesis of Benzo[n.1.0] Bicycloalkanes
    • Ye, L.-W.; Sun, X.-L.; Li, C.-Y.; Tang, Y. Tetrahydrothiophene-Catalyzed Synthesis of Benzo[n.1.0] Bicycloalkanes. J. Org. Chem. 2007, 72, 1335-1340.
    • (2007) J. Org. Chem , vol.72 , pp. 1335-1340
    • Ye, L.-W.1    Sun, X.-L.2    Li, C.-Y.3    Tang, Y.4
  • 48
    • 34547781801 scopus 로고    scopus 로고
    • Phosphine-Catalyzed Intramolecular Formal [3 + 2] Cycloaddition for Highly Diastereoselective Synthesis of Bicyclo[n.3.0] Compounds
    • Ye, L.-W.; Sun, X.-L.; Wang, Q.-G.; Tang, Y. Phosphine-Catalyzed Intramolecular Formal [3 + 2] Cycloaddition for Highly Diastereoselective Synthesis of Bicyclo[n.3.0] Compounds. Angew. Chem., Int. Ed. 2007, 46, 5951-5954.
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 5951-5954
    • Ye, L.-W.1    Sun, X.-L.2    Wang, Q.-G.3    Tang, Y.4
  • 49
    • 37649005243 scopus 로고    scopus 로고
    • 3-Catalyzed Ylide Cyclization for the Controllable Synthesis of Benzobicyclo[4.3.0] Compounds: Base Effects and Scope. Tetrahedron 2008, 64 (7), 1487-1493.
    • 3-Catalyzed Ylide Cyclization for the Controllable Synthesis of Benzobicyclo[4.3.0] Compounds: Base Effects and Scope. Tetrahedron 2008, 64 (7), 1487-1493.
  • 50
    • 51649119436 scopus 로고    scopus 로고
    • Unpublished results
    • Ye, L.-W.; Tang, Y. Unpublished results.
    • Ye, L.-W.1    Tang, Y.2
  • 51
    • 4344612772 scopus 로고    scopus 로고
    • Naturally Occurring Cyclohexane Epoxides: Sources, Biological Activities, and Synthesis
    • Marco-Contelles, J.; Molina, M. T.; Anjum, S. Naturally Occurring Cyclohexane Epoxides: Sources, Biological Activities, and Synthesis. Chem. Rev. 2004, 104, 2857.
    • (2004) Chem. Rev , vol.104 , pp. 2857
    • Marco-Contelles, J.1    Molina, M.T.2    Anjum, S.3
  • 52
    • 42949110730 scopus 로고    scopus 로고
    • Tandem Michael Addition/Ylide Epoxidation for the Synthesis of Highly Functionalized Cyclohexadiene Epoxide Derivatives
    • Wang, Q.-G.; Deng, X.-M.; Zhu, B.-H.; Ye, L.-W.; Sun, X.-L.; Li, C.-Y.; Zhu, C.-Y.; Shen, Q.; Tang, Y. Tandem Michael Addition/Ylide Epoxidation for the Synthesis of Highly Functionalized Cyclohexadiene Epoxide Derivatives. J. Am. Chem. Soc. 2008, 130, 5408-5409.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 5408-5409
    • Wang, Q.-G.1    Deng, X.-M.2    Zhu, B.-H.3    Ye, L.-W.4    Sun, X.-L.5    Li, C.-Y.6    Zhu, C.-Y.7    Shen, Q.8    Tang, Y.9
  • 53
    • 33748605775 scopus 로고
    • Chiral Aziridines - Their Synthesis and Use in Stereoselective Transformations
    • (a) Tanner, D. Chiral Aziridines - Their Synthesis and Use in Stereoselective Transformations. Angew. Chem., Int. Ed. 1994, 33, 599-619.
    • (1994) Angew. Chem., Int. Ed , vol.33 , pp. 599-619
    • Tanner, D.1
  • 54
    • 0030907093 scopus 로고    scopus 로고
    • The Asymmetric Synthesis of Aziridines
    • (b) Osborn, H. M. I.; Sweeney, J. B. The Asymmetric Synthesis of Aziridines. Tetrahedron: Asymmetry 1997, 8, 1693-1715.
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 1693-1715
    • Osborn, H.M.I.1    Sweeney, J.B.2
  • 55
    • 3242750572 scopus 로고    scopus 로고
    • A Facile Reaction of Imines with Telluronium Allylide. Highly Stereoselective Synthesis of Vinylaziridines
    • Liao, W.-W.; Deng, X.-M.; Tang, Y. A Facile Reaction of Imines with Telluronium Allylide. Highly Stereoselective Synthesis of Vinylaziridines. Chem. Commun. 2004, 13, 1516-1517.
    • (2004) Chem. Commun , vol.13 , pp. 1516-1517
    • Liao, W.-W.1    Deng, X.-M.2    Tang, Y.3
  • 56
    • 30144442328 scopus 로고    scopus 로고
    • Telluronium Salts Mediated Aziridination of Chiral N-tert-Butylsulfinylimines: Highly Stereoselective Synthesis of Optically Active Vinylaziridines
    • Zheng, J.-C.; Liao, W.-W.; Sun, X.-X.; Sun, X.-L.; Tang, Y.; Dai, L.-X.; Deng, J.-G. Telluronium Salts Mediated Aziridination of Chiral N-tert-Butylsulfinylimines: Highly Stereoselective Synthesis of Optically Active Vinylaziridines. Org. Lett. 2005, 7, 5789-5792.
    • (2005) Org. Lett , vol.7 , pp. 5789-5792
    • Zheng, J.-C.1    Liao, W.-W.2    Sun, X.-X.3    Sun, X.-L.4    Tang, Y.5    Dai, L.-X.6    Deng, J.-G.7
  • 57
    • 0037652213 scopus 로고    scopus 로고
    • An Efficient Catalytic Ylide Route to Vinyl Epoxides
    • Li, K.; Huang, Z.-Z.; Tang, Y. An Efficient Catalytic Ylide Route to Vinyl Epoxides. Tetrahedron Lett. 2003, 44, 4137-4140.
    • (2003) Tetrahedron Lett , vol.44 , pp. 4137-4140
    • Li, K.1    Huang, Z.-Z.2    Tang, Y.3
  • 58
    • 0042066450 scopus 로고    scopus 로고
    • A Facile Tetrahydrothiophene-catalyzed Ylide Route to Vinyloxiranes
    • Li, K.; Deng, X.-M.; Tang, Y. A Facile Tetrahydrothiophene-catalyzed Ylide Route to Vinyloxiranes. Chem. Commun. 2003, 2074-2075.
    • (2003) Chem. Commun , pp. 2074-2075
    • Li, K.1    Deng, X.-M.2    Tang, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.