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Volumn 47, Issue 8, 2014, Pages 2260-2272

Side arm strategy for catalyst design: Modifying bisoxazolines for remote control of enantioselection and related

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EID: 84906283659     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/ar800104y     Document Type: Article
Times cited : (213)

References (63)
  • 2
    • 0032536002 scopus 로고    scopus 로고
    • 2-symmetric chiral bis(oxazoline)-metal complexes in catalytic asymmetric synthesis
    • 2-symmetric chiral bis(oxazoline)-metal complexes in catalytic asymmetric synthesis Tetrahedron: Asymmetry 1998, 9, 1-45
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 1-45
    • Ghosh, A.K.1    Mathivanan, P.2    Cappiello, J.3
  • 3
    • 0032772355 scopus 로고    scopus 로고
    • Catalytic asymmetric addition reactions of carbonyls. A common catalytic approach
    • Jørgensen, K. A.; Johannsen, M.; Yao, S.; Audrain, H.; Thorhauge, J. Catalytic asymmetric addition reactions of carbonyls. A common catalytic approach Acc. Chem. Res. 1999, 32, 605-613
    • (1999) Acc. Chem. Res. , vol.32 , pp. 605-613
    • Jørgensen, K.A.1    Johannsen, M.2    Yao, S.3    Audrain, H.4    Thorhauge, J.5
  • 4
    • 0033936085 scopus 로고    scopus 로고
    • Chiral bis(oxazoline) copper(II) complexes: Versatile catalysts for enantioselective cycloaddition, aldol, Michael and carbonyl ene reactions
    • Johnson, J. S.; Evans, D. A. Chiral bis(oxazoline) copper(II) complexes: Versatile catalysts for enantioselective cycloaddition, aldol, Michael and carbonyl ene reactions Acc. Chem. Res. 2000, 33, 325-335
    • (2000) Acc. Chem. Res. , vol.33 , pp. 325-335
    • Johnson, J.S.1    Evans, D.A.2
  • 5
    • 84978981855 scopus 로고
    • Enantioselective allylic oxidation using biomimetic tris(oxazolines)- copper(II) complex
    • Kawasaki, K.; Tsumura, S.; Katsuki, T. Enantioselective allylic oxidation using biomimetic tris(oxazolines)-copper(II) complex Synlett 1995, 1245-1246
    • (1995) Synlett , pp. 1245-1246
    • Kawasaki, K.1    Tsumura, S.2    Katsuki, T.3
  • 6
    • 0034116893 scopus 로고    scopus 로고
    • 3-symmetric tris(oxazoline)s derived from Kemps triacid
    • 3-symmetric tris(oxazoline)s derived from Kemps triacid Synth. Commun. 2000, 30, 1627-1641
    • (2000) Synth. Commun. , vol.30 , pp. 1627-1641
    • Chuang, T.H.1    Fang, J.M.2    Bolm, C.3
  • 9
    • 4544385387 scopus 로고    scopus 로고
    • 3-symmetrical chiral trisoxazoline zinc complex as a functional model for zinc hydrolases: Kinetic resolution of racemic chiral esters by transesterification
    • 3-symmetrical chiral trisoxazoline zinc complex as a functional model for zinc hydrolases: Kinetic resolution of racemic chiral esters by transesterification Angew. Chem., Int. Ed. 2004, 43, 4479-4482
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 4479-4482
    • Dro, C.1    Bellemin-Laponnaz, S.2    Welter, R.3    Gade, L.H.4
  • 10
    • 17044371606 scopus 로고    scopus 로고
    • 3 chirality in polymerization catalysis: A highly active dicationic scandium(III) catalyst for the isoselective polymerization of 1-hexene
    • 3 chirality in polymerization catalysis: A highly active dicationic scandium(III) catalyst for the isoselective polymerization of 1-hexene Angew. Chem., Int. Ed. 2005, 44, 1668-1671
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 1668-1671
    • Ward, B.D.1    Bellemin-Laponnaz, S.2    Gade, L.H.3
  • 11
    • 33645526871 scopus 로고    scopus 로고
    • Bisoxazolines with one and two sidearms: Stereodirecting ligands for copper-catalysed asymmetric allylic oxidations of alkenes
    • Seitz, M.; Capacchione, C.; Bellemin-Laponnaz, S.; Wadepohl, H.; Ward, B. D.; Gade, L. H. Bisoxazolines with one and two sidearms: stereodirecting ligands for copper-catalysed asymmetric allylic oxidations of alkenes Dalton Trans. 2006, 193-202
    • (2006) Dalton Trans. , pp. 193-202
    • Seitz, M.1    Capacchione, C.2    Bellemin-Laponnaz, S.3    Wadepohl, H.4    Ward, B.D.5    Gade, L.H.6
  • 12
    • 34547218099 scopus 로고    scopus 로고
    • Using a tripod as a chiral chelating ligand: Chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris (oxazolinyl) ethane ("Trisox")
    • Foltz, C.; Enders, M.; Bellemin-Laponnaz, S.; Wadepohl, H.; Gade, L. H. Using a tripod as a chiral chelating ligand: Chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris (oxazolinyl) ethane ("Trisox") Chem.-Eur. J. 2007, 13, 5994-6008
    • (2007) Chem.-Eur. J. , vol.13 , pp. 5994-6008
    • Foltz, C.1    Enders, M.2    Bellemin-Laponnaz, S.3    Wadepohl, H.4    Gade, L.H.5
  • 13
    • 53549091270 scopus 로고    scopus 로고
    • Exploiting threefold symmetry in asymmetric catalysis: The case of tris(oxazolinyl)ethanes ("trisox")
    • Gade, L. H.; Bellemin-Laponnaz, S. Exploiting threefold symmetry in asymmetric catalysis: The case of tris(oxazolinyl)ethanes ("trisox") Chem.-Eur. J. 2008, 14, 4142-4152
    • (2008) Chem.-Eur. J. , vol.14 , pp. 4142-4152
    • Gade, L.H.1    Bellemin-Laponnaz, S.2
  • 15
    • 0037036814 scopus 로고    scopus 로고
    • Sidearm effect: Improvement of the enantiomeric excess in the asymmetric Michael addition of indoles to alkylidene malonates
    • Zhou, J.; Tang, Y. Sidearm effect: Improvement of the enantiomeric excess in the asymmetric Michael addition of indoles to alkylidene malonates J. Am. Chem. Soc. 2002, 124, 9030-9031
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 9030-9031
    • Zhou, J.1    Tang, Y.2
  • 16
    • 23644450181 scopus 로고    scopus 로고
    • The development and application of chiral trisoxazolines in asymmetric catalysis and molecular recognition
    • Zhou, J.; Tang, Y. The development and application of chiral trisoxazolines in asymmetric catalysis and molecular recognition Chem. Soc. Rev. 2005, 34, 664-676
    • (2005) Chem. Soc. Rev. , vol.34 , pp. 664-676
    • Zhou, J.1    Tang, Y.2
  • 17
    • 0035825178 scopus 로고    scopus 로고
    • Catalytic asymmetric Friedel-Crafts alkylation of beta,gamma-unsaturated alpha-ketoesters: Enantioselective addition of aromatic C-H bonds to alkenes
    • Jensen, K. B.; Thorhauge, J.; Hazell, R. G.; Jorgensen, K. A. Catalytic asymmetric Friedel-Crafts alkylation of beta,gamma-unsaturated alpha-ketoesters: Enantioselective addition of aromatic C-H bonds to alkenes Angew. Chem., Int. Ed. 2001, 40, 160-163
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 160-163
    • Jensen, K.B.1    Thorhauge, J.2    Hazell, R.G.3    Jorgensen, K.A.4
  • 18
    • 0035925220 scopus 로고    scopus 로고
    • Catalytic enantioselective alkylation of heteroaromatic compounds using alkylidene malonates
    • Zhuang, W.; Hansen, T.; Jorgensen, K. A. Catalytic enantioselective alkylation of heteroaromatic compounds using alkylidene malonates Chem. Commun. 2001, 347-348
    • (2001) Chem. Commun. , pp. 347-348
    • Zhuang, W.1    Hansen, T.2    Jorgensen, K.A.3
  • 19
    • 22244469405 scopus 로고    scopus 로고
    • Modular synthesis of chiral homo- and hetero-trisoxazolines. Improving the enantioselectivity in the asymmetric Michael addition of indole to benzylidene malonate
    • Ye, M.-C.; Li, B.; Zhou, J.; Sun, X.-L.; Tang, Y. Modular synthesis of chiral homo- and hetero-trisoxazolines. Improving the enantioselectivity in the asymmetric Michael addition of indole to benzylidene malonate J. Org. Chem. 2005, 70, 6108-6110
    • (2005) J. Org. Chem. , vol.70 , pp. 6108-6110
    • Ye, M.-C.1    Li, B.2    Zhou, J.3    Sun, X.-L.4    Tang, Y.5
  • 20
    • 2542632030 scopus 로고    scopus 로고
    • Sidearm approach: A promising strategy for construction of bisoxazoline-based ligand library
    • Zhou, J.; Ye, M.-C.; Tang, Y. Sidearm approach: A promising strategy for construction of bisoxazoline-based ligand library J. Comb. Chem. 2004, 6, 301-304
    • (2004) J. Comb. Chem. , vol.6 , pp. 301-304
    • Zhou, J.1    Ye, M.-C.2    Tang, Y.3
  • 22
    • 67650538314 scopus 로고    scopus 로고
    • Trisoxazoline/Cu(II)-catalyzed asymmetric intramolecular Friedel-Crafts alkylation reaction of indoles
    • Zhou, J.-L.; Ye, M.-C.; Sun, X.-L.; Tang, Y. Trisoxazoline/Cu(II)- catalyzed asymmetric intramolecular Friedel-Crafts alkylation reaction of indoles Tetrahedron 2009, 65, 6877-6881
    • (2009) Tetrahedron , vol.65 , pp. 6877-6881
    • Zhou, J.-L.1    Ye, M.-C.2    Sun, X.-L.3    Tang, Y.4
  • 23
    • 53149134988 scopus 로고    scopus 로고
    • 2/trisoxazoline catalyzed asymmetric Friedel-Crafts reaction of pyrroles with alkylidene malonates
    • 2/ trisoxazoline catalyzed asymmetric Friedel-Crafts reaction of pyrroles with alkylidene malonates Tetrahedron 2008, 64, 10676-10680
    • (2008) Tetrahedron , vol.64 , pp. 10676-10680
    • Cao, C.-L.1    Zhou, Y.-Y.2    Sun, X.-L.3    Tang, Y.4
  • 24
    • 2542592576 scopus 로고    scopus 로고
    • Diastereo- selectivity-switchable and highly enantioselective 1,3-dipolar cycloaddition of nitrones to alkylidene malonates
    • Huang, Z.-Z.; Kang, Y.-B.; Zhou, J.; Ye, M.-C.; Tang, Y. Diastereo- selectivity-switchable and highly enantioselective 1,3-dipolar cycloaddition of nitrones to alkylidene malonates Org. Lett. 2004, 6, 1677-1679
    • (2004) Org. Lett. , vol.6 , pp. 1677-1679
    • Huang, Z.-Z.1    Kang, Y.-B.2    Zhou, J.3    Ye, M.-C.4    Tang, Y.5
  • 26
    • 0142094051 scopus 로고    scopus 로고
    • Chiral tris(oxazoline)/Cu(II) catalyzed coupling of terminal alkynes and nitrones
    • Ye, M.-C.; Zhou, J.; Huang, Z.-Z.; Tang, Y. Chiral tris(oxazoline)/Cu(II) catalyzed coupling of terminal alkynes and nitrones Chem. Commun. 2003, 2554-2555
    • (2003) Chem. Commun. , pp. 2554-2555
    • Ye, M.-C.1    Zhou, J.2    Huang, Z.-Z.3    Tang, Y.4
  • 27
    • 33646245219 scopus 로고    scopus 로고
    • Trisoxazoline/Cu(II)-promoted Kinugasa reaction. Enantioselective synthesis of beta-lactams
    • Ye, M.-C.; Zhou, J.; Tang, Y. Trisoxazoline/Cu(II)-promoted Kinugasa reaction. Enantioselective synthesis of beta-lactams J. Org. Chem. 2006, 71, 3576-3582
    • (2006) J. Org. Chem. , vol.71 , pp. 3576-3582
    • Ye, M.-C.1    Zhou, J.2    Tang, Y.3
  • 28
    • 84861532056 scopus 로고    scopus 로고
    • Tris(oxazoline)/copper-catalyzed coupling of alkynes with nitrones: A highly enantioselective access to beta-lactams
    • Chen, J.-H.; Liao, S.-H.; Sun, X.-L.; Shen, Q.; Tang, Y. Tris(oxazoline)/copper-catalyzed coupling of alkynes with nitrones: a highly enantioselective access to beta-lactams Tetrahedron 2012, 68, 5042-5045
    • (2012) Tetrahedron , vol.68 , pp. 5042-5045
    • Chen, J.-H.1    Liao, S.-H.2    Sun, X.-L.3    Shen, Q.4    Tang, Y.5
  • 29
    • 60849091059 scopus 로고    scopus 로고
    • Ligand-Accelerated asymmetric [1,2]-Stevens rearrangment of sulfur ylides via decomposition of diazomalonates catalyzed by chiral bisoxazoline/copper complex
    • Qu, J.-P.; Xu, Z.-H.; Zhou, J.; Cao, C.-L.; Sun, X.-L.; Dai, L.-X.; Tang, Y. Ligand-Accelerated asymmetric [1,2]-Stevens rearrangment of sulfur ylides via decomposition of diazomalonates catalyzed by chiral bisoxazoline/copper complex Adv. Synth. Catal. 2009, 351, 308-312
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 308-312
    • Qu, J.-P.1    Xu, Z.-H.2    Zhou, J.3    Cao, C.-L.4    Sun, X.-L.5    Dai, L.-X.6    Tang, Y.7
  • 30
    • 84887765888 scopus 로고    scopus 로고
    • A highly efficient and enantioselective intramolecular Cannizzaro reaction under TOX/Cu(II) catalysis
    • Wang, P.; Tao, W.-J.; Liao, S.; Tang, Y. A highly efficient and enantioselective intramolecular Cannizzaro reaction under TOX/Cu(II) catalysis J. Am. Chem. Soc. 2013, 135, 16849-16852
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 16849-16852
    • Wang, P.1    Tao, W.-J.2    Liao, S.3    Tang, Y.4
  • 31
    • 34250847704 scopus 로고    scopus 로고
    • Sidearm effects in the enantioselective cyclopropanation of alkenes with aryldiazoacetates catalyzed by trisoxazoline/Cu(I)
    • Xu, Z.-H.; Zhu, S.-N.; Sun, X.-L.; Tang, Y.; Dai, L.-X. Sidearm effects in the enantioselective cyclopropanation of alkenes with aryldiazoacetates catalyzed by trisoxazoline/Cu(I) Chem. Commun. 2007, 1960-1962
    • (2007) Chem. Commun. , pp. 1960-1962
    • Xu, Z.-H.1    Zhu, S.-N.2    Sun, X.-L.3    Tang, Y.4    Dai, L.-X.5
  • 33
    • 84868581747 scopus 로고    scopus 로고
    • A chiral cagelike copper(I) catalyst for the highly enantioselective synthesis of 1,1-cyclopropane diesters
    • Deng, C.; Wang, L.-J.; Zhu, J.; Tang, Y. A chiral cagelike copper(I) catalyst for the highly enantioselective synthesis of 1,1-cyclopropane diesters Angew. Chem., Int. Ed. 2012, 51, 11620-11623
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 11620-11623
    • Deng, C.1    Wang, L.-J.2    Zhu, J.3    Tang, Y.4
  • 34
    • 34250782234 scopus 로고    scopus 로고
    • Highly enantioselective and diastereoselective cycloaddition of cyclopropanes with nitrones and its application in the kinetic resolution of 2-substituted cyclopropane-1,1-dicarboxylates
    • Kang, Y.-B.; Sun, X.-L.; Tang, Y. Highly enantioselective and diastereoselective cycloaddition of cyclopropanes with nitrones and its application in the kinetic resolution of 2-substituted cyclopropane-1,1- dicarboxylates Angew. Chem., Int. Ed. 2007, 46, 3918-3921
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 3918-3921
    • Kang, Y.-B.1    Sun, X.-L.2    Tang, Y.3
  • 35
    • 84861864713 scopus 로고    scopus 로고
    • Side-Arm-promoted highly enantioselective ring-opening reactions and kinetic resolution of donor-Acceptor cyclopropanes with amines
    • Zhou, Y.-Y.; Wang, L.-J.; Li, J.; Sun, X.-L.; Tang, Y. Side-Arm-promoted highly enantioselective ring-opening reactions and kinetic resolution of donor-Acceptor cyclopropanes with amines J. Am. Chem. Soc. 2012, 134, 9066-9069
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 9066-9069
    • Zhou, Y.-Y.1    Wang, L.-J.2    Li, J.3    Sun, X.-L.4    Tang, Y.5
  • 36
    • 84872837213 scopus 로고    scopus 로고
    • Highly enantioselective [3 + 3] cycloaddition of aromatic azomethine imines with cyclopropanes directed by pi-pi stacking interactions
    • Zhou, Y.-Y.; Li, J.; Ling, L.; Liao, S.-H.; Sun, X.-L.; Li, Y.-X.; Wang, L.-J.; Tang, Y. Highly enantioselective [3 + 3] cycloaddition of aromatic azomethine imines with cyclopropanes directed by pi-pi stacking interactions Angew. Chem., Int. Ed. 2013, 52, 1452-1456
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 1452-1456
    • Zhou, Y.-Y.1    Li, J.2    Ling, L.3    Liao, S.-H.4    Sun, X.-L.5    Li, Y.-X.6    Wang, L.-J.7    Tang, Y.8
  • 37
    • 84875759358 scopus 로고    scopus 로고
    • Highly enantioselective [3 + 2] annulation of cyclic enol silyl ethers with donoracceptor cyclopropanes: Accessing 3a-hydroxy [n.3.0]carbobicycles
    • Xu, H.; Qu, J.-P.; Liao, S.-H.; Xiong, H.; Tang, Y. Highly enantioselective [3 + 2] annulation of cyclic enol silyl ethers with donoracceptor cyclopropanes: Accessing 3a-hydroxy [n.3.0]carbobicycles Angew. Chem., Int. Ed. 2013, 52, 4004-4007
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 4004-4007
    • Xu, H.1    Qu, J.-P.2    Liao, S.-H.3    Xiong, H.4    Tang, Y.5
  • 38
    • 84878416756 scopus 로고    scopus 로고
    • Copper-catalyzed highly enantioselective cyclopentannulation of indoles with donor-Acceptor cyclopropanes
    • Xiong, H.; Xu, H.; Liao, S.-H.; Xie, Z.; Tang, Y. Copper-catalyzed highly enantioselective cyclopentannulation of indoles with donor-Acceptor cyclopropanes J. Am. Chem. Soc. 2013, 135, 7851-7854
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 7851-7854
    • Xiong, H.1    Xu, H.2    Liao, S.-H.3    Xie, Z.4    Tang, Y.5
  • 39
    • 67650538314 scopus 로고    scopus 로고
    • Trisoxazoline/Cu(II)-catalyzed asymmetric intramolecular Friedel-Crafts alkylation reaction of indoles
    • Zhou, J.-L.; Ye, M.-C.; Sun, X.-L.; Tang, Y. Trisoxazoline/Cu(II)- catalyzed asymmetric intramolecular Friedel-Crafts alkylation reaction of indoles Tetrahedron 2009, 65, 6877-6881
    • (2009) Tetrahedron , vol.65 , pp. 6877-6881
    • Zhou, J.-L.1    Ye, M.-C.2    Sun, X.-L.3    Tang, Y.4
  • 40
    • 79954622936 scopus 로고    scopus 로고
    • Modification of pseudo-C-3-symmetric trisoxazoline and its application to the Friedel-Crafts alkylation of indoles and pyrrole with alkylidene malonates
    • Zhou, Y.-Y.; Sun, X.-L.; Zhu, B.-H.; Zheng, J.-C.; Zhou, J.-L.; Tang, Y. Modification of pseudo-C-3-symmetric trisoxazoline and its application to the Friedel-Crafts alkylation of indoles and pyrrole with alkylidene malonates Synlett 2011, 935-938
    • (2011) Synlett , pp. 935-938
    • Zhou, Y.-Y.1    Sun, X.-L.2    Zhu, B.-H.3    Zheng, J.-C.4    Zhou, J.-L.5    Tang, Y.6
  • 41
    • 0346656521 scopus 로고    scopus 로고
    • Catalytic asymmetric Nazarov reactions promoted by chiral Lewis acid complexes
    • Aggarwal, V. K.; Belfield, A. J. Catalytic asymmetric Nazarov reactions promoted by chiral Lewis acid complexes Org. Lett. 2003, 5, 5075-5078
    • (2003) Org. Lett. , vol.5 , pp. 5075-5078
    • Aggarwal, V.K.1    Belfield, A.J.2
  • 42
    • 3543126652 scopus 로고    scopus 로고
    • Enantioselective Nazarov reactions through catalytic asymmetric proton transfer
    • Liang, G. X.; Trauner, D. Enantioselective Nazarov reactions through catalytic asymmetric proton transfer J. Am. Chem. Soc. 2004, 126, 9544-9545
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 9544-9545
    • Liang, G.X.1    Trauner, D.2
  • 43
    • 0041806585 scopus 로고    scopus 로고
    • A homo [3 + 2] dipolar cycloaddition: The reaction of nitrones with cyclopropanes
    • Young, I. S.; Kerr, M. A. A homo [3 + 2] dipolar cycloaddition: The reaction of nitrones with cyclopropanes Angew. Chem., Int. Ed. 2003, 42, 3023-3026
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 3023-3026
    • Young, I.S.1    Kerr, M.A.2
  • 44
    • 17744393466 scopus 로고    scopus 로고
    • Enantioselective addition of nitrones to activated cyclopropanes
    • Sibi, M. P.; Ma, Z. H.; Jasperse, C. P. Enantioselective addition of nitrones to activated cyclopropanes J. Am. Chem. Soc. 2005, 127, 5764-5765
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 5764-5765
    • Sibi, M.P.1    Ma, Z.H.2    Jasperse, C.P.3
  • 45
    • 51549111915 scopus 로고    scopus 로고
    • A mild procedure for the Lewis acid-catalyzed ring-opening of activated cyclopropanes with amine nucleophiles
    • Lifchits, O.; Charette, A. B. A mild procedure for the Lewis acid-catalyzed ring-opening of activated cyclopropanes with amine nucleophiles Org. Lett. 2008, 10, 2809-2812
    • (2008) Org. Lett. , vol.10 , pp. 2809-2812
    • Lifchits, O.1    Charette, A.B.2
  • 46
    • 84863157939 scopus 로고    scopus 로고
    • Highly diastereoselective construction of fused carbocycles from cyclopropane-1,1-dicarboxylates and cyclic enol silyl ethers: Scope, mechanism, and origin of diastereoselectivity
    • Qu, J.-P.; Liang, Y.; Xu, H.; Sun, X.-L.; Yu, Z.-X.; Tang, Y. Highly diastereoselective construction of fused carbocycles from cyclopropane-1,1- dicarboxylates and cyclic enol silyl ethers: Scope, mechanism, and origin of diastereoselectivity Chem.-Eur. J. 2012, 18, 2196-2201
    • (2012) Chem.-Eur. J. , vol.18 , pp. 2196-2201
    • Qu, J.-P.1    Liang, Y.2    Xu, H.3    Sun, X.-L.4    Yu, Z.-X.5    Tang, Y.6
  • 47
    • 67749106330 scopus 로고    scopus 로고
    • Catalytic enantioselective synthesis of tetrahydrofurans: A dynamic kinetic asymmetric [3 + 2] cycloaddition of racemic cyclopropanes and aldehydes
    • Parsons, A. T.; Johnson, J. S. Catalytic enantioselective synthesis of tetrahydrofurans: A dynamic kinetic asymmetric [3 + 2] cycloaddition of racemic cyclopropanes and aldehydes J. Am. Chem. Soc. 2009, 131, 3122-3123
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3122-3123
    • Parsons, A.T.1    Johnson, J.S.2
  • 48
    • 49949143547 scopus 로고
    • Asymmetric induction in carbenoid reaction by means of a dissymmetric copper chelate
    • Nozaki, H.; Moriuti, S.; Takaya, H.; Noyori, R. Asymmetric induction in carbenoid reaction by means of a dissymmetric copper chelate Tetrahedron Lett. 1966, 5239-5244
    • (1966) Tetrahedron Lett. , pp. 5239-5244
    • Nozaki, H.1    Moriuti, S.2    Takaya, H.3    Noyori, R.4
  • 49
    • 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, 911-935
    • (1998) Chem. Rev. , vol.98 , pp. 911-935
    • Doyle, M.P.1    Forbes, D.C.2
  • 51
    • 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
  • 52
    • 10844247257 scopus 로고    scopus 로고
    • One-pot synthesis and chiral analysis of cyclopropane derivatives
    • Ghanem, A.; Aboul-Enein, H. Y.; Muller, P. One-pot synthesis and chiral analysis of cyclopropane derivatives Chirality 2005, 17, 44-50
    • (2005) Chirality , vol.17 , pp. 44-50
    • Ghanem, A.1    Aboul-Enein, H.Y.2    Muller, P.3
  • 53
    • 0029089453 scopus 로고
    • Copper-catalyzed reaction of terminal alkynes with nitrones - Selective synthesis of 1-Aza-1-buten-3-yne and 2-Azetidinone derivatives
    • Miura, M.; Enna, M.; Okuro, K.; Nomura, M. Copper-catalyzed reaction of terminal alkynes with nitrones-selective synthesis of 1-Aza-1-buten-3-yne and 2-Azetidinone derivatives J. Org. Chem. 1995, 60, 4999-5004
    • (1995) J. Org. Chem. , vol.60 , pp. 4999-5004
    • Miura, M.1    Enna, M.2    Okuro, K.3    Nomura, M.4
  • 56
    • 84875918173 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of multifunctionalized dihydrofurans by copper-catalyzed asymmetric [4 + 1] cycloadditions of α-benzylidene- β-ketoester with diazo compound
    • Zhou, J.-L.; Wang, L.-J.; Xu, H.; Sun, X.-L.; Tang, Y. Highly enantioselective synthesis of multifunctionalized dihydrofurans by copper-catalyzed asymmetric [4 + 1] cycloadditions of α-benzylidene- β-ketoester with diazo compound ACS Catal. 2013, 3, 685-688
    • (2013) ACS Catal. , vol.3 , pp. 685-688
    • Zhou, J.-L.1    Wang, L.-J.2    Xu, H.3    Sun, X.-L.4    Tang, Y.5
  • 57
    • 33846817249 scopus 로고    scopus 로고
    • Copper-catalyzed asymmetric [4 + 1] cycloadditions of enones with diazo compounds to form dihydrofurans
    • Son, S.; Fu, G. C. Copper-catalyzed asymmetric [4 + 1] cycloadditions of enones with diazo compounds to form dihydrofurans J. Am. Chem. Soc. 2007, 129, 1046-1047
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1046-1047
    • Son, S.1    Fu, G.C.2
  • 58
    • 52149096264 scopus 로고    scopus 로고
    • Asymmetric intramolecular Cannizzaro reaction of anhydrous phenylglyoxal
    • Ishihara, K.; Yano, T.; Fushimi, M. Asymmetric intramolecular Cannizzaro reaction of anhydrous phenylglyoxal J. Fluorine Chem. 2008, 129, 994-997
    • (2008) J. Fluorine Chem. , vol.129 , pp. 994-997
    • Ishihara, K.1    Yano, T.2    Fushimi, M.3
  • 59
    • 0034548896 scopus 로고    scopus 로고
    • Efficient Lewis acid catalyzed intramolecular Cannizzaro reaction
    • Russell, A. E.; Miller, S. P.; Morken, J. P. Efficient Lewis acid catalyzed intramolecular Cannizzaro reaction J. Org. Chem. 2000, 65, 8381-8383
    • (2000) J. Org. Chem. , vol.65 , pp. 8381-8383
    • Russell, A.E.1    Miller, S.P.2    Morken, J.P.3
  • 61
    • 0037012915 scopus 로고    scopus 로고
    • Wittig-type olefination catalyzed by PEG-telluride
    • Huang, Z.-Z.; Ye, S.; Xia, W.; Yu, Y.-H.; Tang, Y. Wittig-type olefination catalyzed by PEG-telluride J. Org. Chem. 2002, 67, 3096-3103
    • (2002) J. Org. Chem. , vol.67 , pp. 3096-3103
    • Huang, Z.-Z.1    Ye, S.2    Xia, W.3    Yu, Y.-H.4    Tang, Y.5
  • 62
    • 68949163231 scopus 로고    scopus 로고
    • Combining fluorous and triazole moieties for the tagging of chiral azabis(oxazoline) ligands
    • Rasappan, R.; Olbrich, T.; Reiser, O. Combining fluorous and triazole moieties for the tagging of chiral azabis(oxazoline) ligands Adv. Synth. Catal. 2009, 351, 1961-1967
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 1961-1967
    • Rasappan, R.1    Olbrich, T.2    Reiser, O.3
  • 63
    • 79955413969 scopus 로고    scopus 로고
    • An enantioselective synthesis of 2-Aryl cycloalkanones by Sc-catalyzed carbon insertion
    • Rendina, V. L.; Moebius, D. C.; Kingsbury, J. S. An enantioselective synthesis of 2-Aryl cycloalkanones by Sc-catalyzed carbon insertion Org. Lett. 2011, 13, 2004-2007
    • (2011) Org. Lett. , vol.13 , pp. 2004-2007
    • Rendina, V.L.1    Moebius, D.C.2    Kingsbury, J.S.3


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