메뉴 건너뛰기




Volumn 55, Issue 24, 2016, Pages 12500-12503

Chiral Cu(salen)-Based Metal-Organic Framework for Heterogeneously Catalyzed Aziridination and Amination of Olefins

Author keywords

[No Author keywords available]

Indexed keywords


EID: 85006757550     PISSN: 00201669     EISSN: 1520510X     Source Type: Journal    
DOI: 10.1021/acs.inorgchem.6b02151     Document Type: Article
Times cited : (42)

References (56)
  • 1
    • 1642381914 scopus 로고    scopus 로고
    • Heterogeneous enantioselective catalysts: Strategies for the immobilisation of homogeneous catalysts
    • McMorn, P.; Hutchings, G. J. Heterogeneous enantioselective catalysts: strategies for the immobilisation of homogeneous catalysts Chem. Soc. Rev. 2004, 33, 108-122 10.1039/b200387m
    • (2004) Chem. Soc. Rev. , vol.33 , pp. 108-122
    • McMorn, P.1    Hutchings, G.J.2
  • 2
    • 51649113927 scopus 로고    scopus 로고
    • Reactivity of surface alkoxy species on acidic zeolite catalysts
    • Wang, W.; Hunger, M. Reactivity of surface alkoxy species on acidic zeolite catalysts Acc. Chem. Res. 2008, 41, 895-904 10.1021/ar700210f
    • (2008) Acc. Chem. Res. , vol.41 , pp. 895-904
    • Wang, W.1    Hunger, M.2
  • 3
    • 65349139123 scopus 로고    scopus 로고
    • Organic polymer supports for synthesis and for reagent and catalyst immobilization
    • Lu, J.; Toy, P. H. Organic polymer supports for synthesis and for reagent and catalyst immobilization Chem. Rev. 2009, 109, 815-838 10.1021/cr8004444
    • (2009) Chem. Rev. , vol.109 , pp. 815-838
    • Lu, J.1    Toy, P.H.2
  • 4
    • 64549151421 scopus 로고    scopus 로고
    • Recyclable stereoselective catalysts
    • Trindade, A. F.; Gois, P. M. P.; Afonso, C. A. M. Recyclable stereoselective catalysts Chem. Rev. 2009, 109, 418-514 10.1021/cr800200t
    • (2009) Chem. Rev. , vol.109 , pp. 418-514
    • Trindade, A.F.1    Gois, P.M.P.2    Afonso, C.A.M.3
  • 5
    • 84940064424 scopus 로고    scopus 로고
    • Metal-organic frameworks: Versatile heterogeneous catalysts for efficient catalytic organic transformations
    • Chughtai, A. H.; Ahmad, N.; Younus, H. A.; Laypkov, A.; Verpoort, F. Metal-organic frameworks: versatile heterogeneous catalysts for efficient catalytic organic transformations Chem. Soc. Rev. 2015, 44, 6804-6849 10.1039/C4CS00395K
    • (2015) Chem. Soc. Rev. , vol.44 , pp. 6804-6849
    • Chughtai, A.H.1    Ahmad, N.2    Younus, H.A.3    Laypkov, A.4    Verpoort, F.5
  • 6
    • 77954063984 scopus 로고    scopus 로고
    • Engineering metal organic frameworks for heterogeneous catalysis
    • Corma, A.; García, H.; Llabrés i Xamena, F. X. Engineering metal organic frameworks for heterogeneous catalysis Chem. Rev. 2010, 110, 4606-4655 10.1021/cr9003924
    • (2010) Chem. Rev. , vol.110 , pp. 4606-4655
    • Corma, A.1    García, H.2    Llabrés Xamenai, F.X.3
  • 7
    • 65349140088 scopus 로고    scopus 로고
    • Enantioselective catalysis with homochiral metal-organic frameworks
    • Ma, L.; Abney, C.; Lin, W. Enantioselective catalysis with homochiral metal-organic frameworks Chem. Soc. Rev. 2009, 38, 1248-1256 10.1039/b807083k
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 1248-1256
    • Ma, L.1    Abney, C.2    Lin, W.3
  • 8
    • 84863012695 scopus 로고    scopus 로고
    • Homochiral metal-organic frameworks for asymmetric heterogeneous catalysis
    • Yoon, M.; Srirambalaji, R.; Kim, K. Homochiral metal-organic frameworks for asymmetric heterogeneous catalysis Chem. Rev. 2012, 112, 1196-1231 10.1021/cr2003147
    • (2012) Chem. Rev. , vol.112 , pp. 1196-1231
    • Yoon, M.1    Srirambalaji, R.2    Kim, K.3
  • 9
    • 77957563058 scopus 로고    scopus 로고
    • Engineering homochiral metal-organic frameworks for heterogeneous asymmetric catalysis and enantioselective separation
    • Liu, Y.; Xuan, W.; Cui, Y. Engineering homochiral metal-organic frameworks for heterogeneous asymmetric catalysis and enantioselective separation Adv. Mater. 2010, 22, 4112-4135 10.1002/adma.201000197
    • (2010) Adv. Mater. , vol.22 , pp. 4112-4135
    • Liu, Y.1    Xuan, W.2    Cui, Y.3
  • 10
    • 84883066942 scopus 로고    scopus 로고
    • The chemistry and applications of metal-organic frameworks
    • Furukawa, H.; Cordova, K. E.; O'Keeffe, M.; Yaghi, O. M. The chemistry and applications of metal-organic frameworks Science 2013, 341, 1230444 10.1126/science.1230444
    • (2013) Science , vol.341 , pp. 1230444
    • Furukawa, H.1    Cordova, K.E.2    O'Keeffe, M.3    Yaghi, O.M.4
  • 11
    • 0035384248 scopus 로고    scopus 로고
    • From molecules to crystal engineering: Supramolecular isomerism and polymorphism in network solids
    • Moulton, B.; Zaworotko, M. J. From molecules to crystal engineering: supramolecular isomerism and polymorphism in network solids Chem. Rev. 2001, 101, 1629-1658 10.1021/cr9900432
    • (2001) Chem. Rev. , vol.101 , pp. 1629-1658
    • Moulton, B.1    Zaworotko, M.J.2
  • 12
    • 65149084322 scopus 로고    scopus 로고
    • Hydrogen storage in metal-organic frameworks
    • Murray, L. J.; Dincǎ, M.; Long, J. R. Hydrogen storage in metal-organic frameworks Chem. Soc. Rev. 2009, 38, 1294-1314 10.1039/b802256a
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 1294-1314
    • Murray, L.J.1    Dincǎ, M.2    Long, J.R.3
  • 13
    • 84863011015 scopus 로고    scopus 로고
    • Metal-organic frameworks for separations
    • Li, J.-R.; Sculley, J.; Zhou, H.-C. Metal-organic frameworks for separations Chem. Rev. 2012, 112, 869-932 10.1021/cr200190s
    • (2012) Chem. Rev. , vol.112 , pp. 869-932
    • Li, J.-R.1    Sculley, J.2    Zhou, H.-C.3
  • 15
    • 20344394407 scopus 로고    scopus 로고
    • Design, chirality, and flexibility in nanoporous molecule-based materials
    • Bradshaw, D.; Claridge, J. B.; Cussen, E. J.; Prior, T. J.; Rosseinsky, M. J. Design, chirality, and flexibility in nanoporous molecule-based materials Acc. Chem. Res. 2005, 38, 273-282 10.1021/ar0401606
    • (2005) Acc. Chem. Res. , vol.38 , pp. 273-282
    • Bradshaw, D.1    Claridge, J.B.2    Cussen, E.J.3    Prior, T.J.4    Rosseinsky, M.J.5
  • 16
    • 0042517640 scopus 로고
    • Preparation, clathration ability, and catalysis of a two-dimensional square network material composed of cadmium (II) and 4, 4′-bipyridine
    • Fujita, M.; Kwon, Y. J.; Washizu, S.; Ogura, K. Preparation, clathration ability, and catalysis of a two-dimensional square network material composed of cadmium (II) and 4, 4′-bipyridine J. Am. Chem. Soc. 1994, 116, 1151-1152 10.1021/ja00082a055
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 1151-1152
    • Fujita, M.1    Kwon, Y.J.2    Washizu, S.3    Ogura, K.4
  • 17
    • 0001412882 scopus 로고    scopus 로고
    • A homochiral metal-organic porous material for enantioselective separation and catalysis
    • Kim, K.; Seo, J. S.; Whang, D.; Lee, H.; Jun, S. I.; Oh, J.; Jeon, Y. J. A homochiral metal-organic porous material for enantioselective separation and catalysis Nature 2000, 404, 982-986 10.1038/35010088
    • (2000) Nature , vol.404 , pp. 982-986
    • Kim, K.1    Seo, J.S.2    Whang, D.3    Lee, H.4    Jun, S.I.5    Oh, J.6    Jeon, Y.J.7
  • 19
    • 33847667489 scopus 로고    scopus 로고
    • Three-dimensional porous coordination polymer functionalized with amide groups based on tridentate ligand: Selective sorption and catalysis
    • Hasegawa, S.; Horike, S.; Matsuda, R.; Furukawa, S.; Mochizuki, K.; Kinoshita, Y.; Kitagawa, S. Three-dimensional porous coordination polymer functionalized with amide groups based on tridentate ligand: selective sorption and catalysis J. Am. Chem. Soc. 2007, 129, 2607-2614 10.1021/ja067374y
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 2607-2614
    • Hasegawa, S.1    Horike, S.2    Matsuda, R.3    Furukawa, S.4    Mochizuki, K.5    Kinoshita, Y.6    Kitagawa, S.7
  • 20
    • 32044466464 scopus 로고    scopus 로고
    • A homochiral metal-organic material with permanent porosity, enantioselective sorption properties, and catalytic activity
    • Dybtsev, D. N.; Nuzhdin, A. L.; Chun, H.; Bryliakov, K. P.; Talsi, E. P.; Fedin, V. P.; Kim, K. A homochiral metal-organic material with permanent porosity, enantioselective sorption properties, and catalytic activity Angew. Chem., Int. Ed. 2006, 45, 916-920 10.1002/anie.200503023
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 916-920
    • Dybtsev, D.N.1    Nuzhdin, A.L.2    Chun, H.3    Bryliakov, K.P.4    Talsi, E.P.5    Fedin, V.P.6    Kim, K.7
  • 21
    • 77957287036 scopus 로고    scopus 로고
    • A series of isoreticular chiral metal-organic frameworks as a tunable platform for asymmetric catalysis
    • Ma, L.; Falkowski, J. M.; Abney, C.; Lin, W. A series of isoreticular chiral metal-organic frameworks as a tunable platform for asymmetric catalysis Nat. Chem. 2010, 2, 838 10.1038/nchem.738
    • (2010) Nat. Chem. , vol.2 , pp. 838
    • Ma, L.1    Falkowski, J.M.2    Abney, C.3    Lin, W.4
  • 22
    • 84893727627 scopus 로고    scopus 로고
    • A homochiral metal-organic framework as an effective asymmetric catalyst for cyanohydrin synthesis
    • Mo, K.; Yang, Y.; Cui, Y. A homochiral metal-organic framework as an effective asymmetric catalyst for cyanohydrin synthesis J. Am. Chem. Soc. 2014, 136, 1746-1749 10.1021/ja411887c
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 1746-1749
    • Mo, K.1    Yang, Y.2    Cui, Y.3
  • 23
    • 67650523201 scopus 로고    scopus 로고
    • Postsynthetic modification switches an achiral framework to catalytically active homochiral metal-organic porous materials
    • Banerjee, M.; Das, S.; Yoon, M.; Choi, H. J.; Hyun, M. H.; Park, S. M.; Seo, G.; Kim, K. Postsynthetic modification switches an achiral framework to catalytically active homochiral metal-organic porous materials J. Am. Chem. Soc. 2009, 131, 7524-7525 10.1021/ja901440g
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 7524-7525
    • Banerjee, M.1    Das, S.2    Yoon, M.3    Choi, H.J.4    Hyun, M.H.5    Park, S.M.6    Seo, G.7    Kim, K.8
  • 24
    • 70349917518 scopus 로고    scopus 로고
    • Engineering a metal-organic framework catalyst by using postsynthetic modification
    • Tanabe, K. K.; Cohen, S. M. Engineering a metal-organic framework catalyst by using postsynthetic modification Angew. Chem., Int. Ed. 2009, 48, 7424-7427 10.1002/anie.200903433
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 7424-7427
    • Tanabe, K.K.1    Cohen, S.M.2
  • 25
    • 33745193730 scopus 로고    scopus 로고
    • A metal-organic framework material that functions as an enantioselective catalyst for olefin epoxidation
    • Cho, S. H.; Ma, B. Q.; Nguyen, S. T.; Hupp, J. T.; Albrecht-Schmitt, T. E. A metal-organic framework material that functions as an enantioselective catalyst for olefin epoxidation Chem. Commun. 2006, 2563-2565 10.1039/B600408C
    • (2006) Chem. Commun. , pp. 2563-2565
    • Cho, S.H.1    Ma, B.Q.2    Nguyen, S.T.3    Hupp, J.T.4    Albrecht-Schmitt, T.E.5
  • 26
    • 78049367779 scopus 로고    scopus 로고
    • Isoreticular chiral metal-organic frameworks for asymmetric alkene epoxidation: Tuning catalytic activity by controlling framework catenation and varying open channel sizes
    • Song, F.; Wang, C.; Falkowski, J. M.; Ma, L.; Lin, W. Isoreticular chiral metal-organic frameworks for asymmetric alkene epoxidation: tuning catalytic activity by controlling framework catenation and varying open channel sizes J. Am. Chem. Soc. 2010, 132, 15390-15398 10.1021/ja1069773
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15390-15398
    • Song, F.1    Wang, C.2    Falkowski, J.M.3    Ma, L.4    Lin, W.5
  • 27
    • 79960711687 scopus 로고    scopus 로고
    • Actuation of asymmetric cyclopropanation catalysts: Reversible single-crystal to single-crystal reduction of metal-organic frameworks
    • Falkowski, J. M.; Wang, C.; Liu, S.; Lin, W. Actuation of asymmetric cyclopropanation catalysts: reversible single-crystal to single-crystal reduction of metal-organic frameworks Angew. Chem., Int. Ed. 2011, 50, 8674-8678 10.1002/anie.201104086
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 8674-8678
    • Falkowski, J.M.1    Wang, C.2    Liu, S.3    Lin, W.4
  • 28
    • 84862101923 scopus 로고    scopus 로고
    • Chiral nanoporous metal-metallosalen frameworks for hydrolytic kinetic resolution of epoxides
    • Zhu, C.; Yuan, G.; Chen, X.; Yang, Z.; Cui, Y. Chiral nanoporous metal-metallosalen frameworks for hydrolytic kinetic resolution of epoxides J. Am. Chem. Soc. 2012, 134, 8058-8061 10.1021/ja302340b
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 8058-8061
    • Zhu, C.1    Yuan, G.2    Chen, X.3    Yang, Z.4    Cui, Y.5
  • 29
    • 84904190421 scopus 로고    scopus 로고
    • Engineering chiral Fe(salen)-based metal-organic frameworks for asymmetric sulfide oxidation
    • Yang, Z.; Zhu, C.; Li, Z.; Liu, Y.; Liu, G.; Cui, Y. Engineering chiral Fe(salen)-based metal-organic frameworks for asymmetric sulfide oxidation Chem. Commun. 2014, 50, 8775-8778 10.1039/C4CC03308F
    • (2014) Chem. Commun. , vol.50 , pp. 8775-8778
    • Yang, Z.1    Zhu, C.2    Li, Z.3    Liu, Y.4    Liu, G.5    Cui, Y.6
  • 30
    • 84940438356 scopus 로고    scopus 로고
    • Direct and post-synthesis incorporation of chiral metallosalen catalysts into metal-organic frameworks for asymmetric organic transformations
    • Xi, W.; Liu, Y.; Xia, Q.; Li, Z.; Cui, Y. Direct and post-synthesis incorporation of chiral metallosalen catalysts into metal-organic frameworks for asymmetric organic transformations Chem.-Eur. J. 2015, 21, 12581-12585 10.1002/chem.201501486
    • (2015) Chem. - Eur. J. , vol.21 , pp. 12581-12585
    • Xi, W.1    Liu, Y.2    Xia, Q.3    Li, Z.4    Cui, Y.5
  • 31
    • 79960396493 scopus 로고    scopus 로고
    • A chiral metal-organic framework for sequential asymmetric catalysis
    • Song, F.; Wang, C.; Lin, W. A chiral metal-organic framework for sequential asymmetric catalysis Chem. Commun. 2011, 47, 8256-8258 10.1039/c1cc12701b
    • (2011) Chem. Commun. , vol.47 , pp. 8256-8258
    • Song, F.1    Wang, C.2    Lin, W.3
  • 32
    • 84862166416 scopus 로고    scopus 로고
    • Chiral metal-organic frameworks with tunable open channels as single-site asymmetric cyclopropanation catalysts
    • Falkowski, J. M.; Liu, S.; Wang, C.; Lin, W. Chiral metal-organic frameworks with tunable open channels as single-site asymmetric cyclopropanation catalysts Chem. Commun. 2012, 48, 6508-6510 10.1039/c2cc32232c
    • (2012) Chem. Commun. , vol.48 , pp. 6508-6510
    • Falkowski, J.M.1    Liu, S.2    Wang, C.3    Lin, W.4
  • 33
    • 84864663925 scopus 로고    scopus 로고
    • Blocking bimolecular activation pathways leads to different regioselectivity in metal-organic framework catalysis
    • Zhang, T.; Song, F.; Lin, W. Blocking bimolecular activation pathways leads to different regioselectivity in metal-organic framework catalysis Chem. Commun. 2012, 48, 8766-8768 10.1039/c2cc34033j
    • (2012) Chem. Commun. , vol.48 , pp. 8766-8768
    • Zhang, T.1    Song, F.2    Lin, W.3
  • 34
    • 79955377394 scopus 로고    scopus 로고
    • Selective surface and near-surface modification of a noncatenated, catalytically active metal-organic framework material based on Mn(salen) struts
    • Shultz, A. M.; Farha, O. K.; Adhikari, D.; Sarjeant, A. A.; Hupp, J. T.; Nguyen, S. T. Selective surface and near-surface modification of a noncatenated, catalytically active metal-organic framework material based on Mn(salen) struts Inorg. Chem. 2011, 50, 3174-3176 10.1021/ic101952y
    • (2011) Inorg. Chem. , vol.50 , pp. 3174-3176
    • Shultz, A.M.1    Farha, O.K.2    Adhikari, D.3    Sarjeant, A.A.4    Hupp, J.T.5    Nguyen, S.T.6
  • 35
    • 80052092430 scopus 로고    scopus 로고
    • Post-synthesis modification of a metal-organic framework to form metallosalen-containing MOF materials
    • Shultz, A. M.; Sarjeant, A. A.; Farha, O. K.; Hupp, J. T.; Nguyen, S. T. Post-synthesis modification of a metal-organic framework to form metallosalen-containing MOF materials J. Am. Chem. Soc. 2011, 133, 13252-13255 10.1021/ja204820d
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 13252-13255
    • Shultz, A.M.1    Sarjeant, A.A.2    Farha, O.K.3    Hupp, J.T.4    Nguyen, S.T.5
  • 36
    • 33749855460 scopus 로고    scopus 로고
    • Chiral salen complexes: An overview to recoverable and reusable homogeneous and heterogeneous catalysts
    • Baleizao, C.; Garcia, H. Chiral salen complexes: an overview to recoverable and reusable homogeneous and heterogeneous catalysts Chem. Rev. 2006, 106, 3987-4043 10.1021/cr050973n
    • (2006) Chem. Rev. , vol.106 , pp. 3987-4043
    • Baleizao, C.1    Garcia, H.2
  • 37
    • 0035128046 scopus 로고    scopus 로고
    • Group 13 compounds incorporating salen ligands
    • Atwood, D. A.; Harvey, M. Group 13 compounds incorporating salen ligands Chem. Rev. 2001, 101, 37-52 10.1021/cr990008v
    • (2001) Chem. Rev. , vol.101 , pp. 37-52
    • Atwood, D.A.1    Harvey, M.2
  • 38
    • 27844485724 scopus 로고    scopus 로고
    • A Highly DNA-Duplex-Stabilizing Metal-Salen Base Pair
    • Clever, G. H.; Polborn, K.; Carell, T. A Highly DNA-Duplex-Stabilizing Metal-Salen Base Pair Angew. Chem., Int. Ed. 2005, 44, 7204-7208 10.1002/anie.200501589
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 7204-7208
    • Clever, G.H.1    Polborn, K.2    Carell, T.3
  • 39
    • 0007448978 scopus 로고
    • Asymmetric Alkene Aziridination with Readily Available Chiral Diimine-Based Catalysts
    • Li, Z.; Conser, K. R.; Jacobsen, E. N. Asymmetric Alkene Aziridination with Readily Available Chiral Diimine-Based Catalysts J. Am. Chem. Soc. 1993, 115, 5326-5327 10.1021/ja00065a067
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 5326-5327
    • Li, Z.1    Conser, K.R.2    Jacobsen, E.N.3
  • 40
    • 0028231555 scopus 로고
    • Nonstereospecific Mechanisms in Asymmetric Addition to Alkenes Result in Enantiodifferentiation after the First Irreversible Step
    • Zhang, W.; Lee, N. H.; Jacobsen, E. N. Nonstereospecific Mechanisms in Asymmetric Addition to Alkenes Result in Enantiodifferentiation after the First Irreversible Step J. Am. Chem. Soc. 1994, 116, 425-426 10.1021/ja00080a070
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 425-426
    • Zhang, W.1    Lee, N.H.2    Jacobsen, E.N.3
  • 41
    • 53249126067 scopus 로고    scopus 로고
    • Material applications for salen frameworks
    • Wezenberg, S. J.; Kleij, A. W. Material applications for salen frameworks Angew. Chem., Int. Ed. 2008, 47, 2354-2364 10.1002/anie.200702468
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 2354-2364
    • Wezenberg, S.J.1    Kleij, A.W.2
  • 43
    • 0001792356 scopus 로고    scopus 로고
    • Single-crystal structure validation with the program PLATON
    • Spek, A. L. Single-crystal structure validation with the program PLATON J. Appl. Crystallogr. 2003, 36, 7-13 10.1107/S0021889802022112
    • (2003) J. Appl. Crystallogr. , vol.36 , pp. 7-13
    • Spek, A.L.1
  • 44
    • 51049114031 scopus 로고    scopus 로고
    • Coinage metal-assisted synthesis of heterocycles
    • Patil, N. T.; Yamamoto, Y. Coinage metal-assisted synthesis of heterocycles Chem. Rev. 2008, 108, 3395-3442 10.1021/cr050041j
    • (2008) Chem. Rev. , vol.108 , pp. 3395-3442
    • Patil, N.T.1    Yamamoto, Y.2
  • 45
    • 51049091002 scopus 로고    scopus 로고
    • Coinage Metal Catalyzed C-H Bond Functionalization of Hydrocarbons
    • Díaz-Requejo, M. M.; Pérez, P. J. Coinage Metal Catalyzed C-H Bond Functionalization of Hydrocarbons Chem. Rev. 2008, 108, 3379-3394 10.1021/cr078364y
    • (2008) Chem. Rev. , vol.108 , pp. 3379-3394
    • Díaz-Requejo, M.M.1    Pérez, P.J.2
  • 46
    • 33748605775 scopus 로고
    • Chiral aziridines - Their synthesis and use in stereoselective transformations
    • Tanner, D. Chiral aziridines-their synthesis and use in stereoselective transformations Angew. Chem., Int. Ed. Engl. 1994, 33, 599-619 10.1002/anie.199405991
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 599-619
    • Tanner, D.1
  • 48
    • 33751191335 scopus 로고    scopus 로고
    • Methyeneaziridines: Unusual vehicles for organic synthesis
    • Shipman, M. Methyeneaziridines: unusual vehicles for organic synthesis Synlett 2006, 2006, 3205 10.1055/s-2006-951566
    • (2006) Synlett , vol.2006 , pp. 3205
    • Shipman, M.1
  • 49
    • 0040518632 scopus 로고    scopus 로고
    • Mechanistic studies of copper-catalyzed alkene aziridination
    • Brandt, P.; Södergren, M. J.; Andersson, P. G.; Norrby, P.-O. Mechanistic studies of copper-catalyzed alkene aziridination J. Am. Chem. Soc. 2000, 122, 8013-8020 10.1021/ja993246g
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 8013-8020
    • Brandt, P.1    Södergren, M.J.2    Andersson, P.G.3    Norrby, P.-O.4
  • 50
    • 11644312278 scopus 로고
    • Development of the copper-catalyzed olefin aziridination reaction
    • Evans, D. A.; Faul, M. M.; Bilodeau, M. T. Development of the copper-catalyzed olefin aziridination reaction J. Am. Chem. Soc. 1994, 116, 2742-2753 10.1021/ja00086a007
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 2742-2753
    • Evans, D.A.1    Faul, M.M.2    Bilodeau, M.T.3
  • 51
    • 0000072415 scopus 로고
    • Mechanism of the (Diimine)copper-Catalyzed Asymmetric Aziridination of Alkenes. Nitrene Transfer via Ligand-Accelerated Catalysis
    • Li, Z.; Quan, R. W.; Jacobsen, E. N. Mechanism of the (Diimine)copper-Catalyzed Asymmetric Aziridination of Alkenes. Nitrene Transfer via Ligand-Accelerated Catalysis J. Am. Chem. Soc. 1995, 117, 5889-5890 10.1021/ja00126a044
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5889-5890
    • Li, Z.1    Quan, R.W.2    Jacobsen, E.N.3
  • 52
    • 79960782886 scopus 로고
    • Unusually strong interactions mediated by both.pi.-.Pi. Stacking and CH-.Pi. Interactions present in the dimer of nickel(II) complex coordinated with n-butyl-substituted salen
    • Miyamura, K.; Mihara, A.; Fujii, T.; Gohshi, Y.; Ishii, Y. Unusually strong interactions mediated by both.pi.-.pi. stacking and CH-.pi. interactions present in the dimer of nickel(II) complex coordinated with n-butyl-substituted salen J. Am. Chem. Soc. 1995, 117, 2377-2378 10.1021/ja00113a038
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 2377-2378
    • Miyamura, K.1    Mihara, A.2    Fujii, T.3    Gohshi, Y.4    Ishii, Y.5
  • 53
    • 0344012946 scopus 로고    scopus 로고
    • Ion-induced tubular assembly of conjugated schiff-base macrocycles
    • Gallant, A. J.; MacLachlan, M. J. Ion-induced tubular assembly of conjugated schiff-base macrocycles Angew. Chem., Int. Ed. 2003, 42, 5307-5310 10.1002/anie.200352395
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5307-5310
    • Gallant, A.J.1    MacLachlan, M.J.2
  • 54
    • 47249163245 scopus 로고    scopus 로고
    • Exploiting nanospace for asymmetric catalysis: Confinement of immobilized, single-site chiral catalysts enhances enantioselectivity
    • Thomas, J. M.; Raja, R. Exploiting nanospace for asymmetric catalysis: confinement of immobilized, single-site chiral catalysts enhances enantioselectivity Acc. Chem. Res. 2008, 41, 708-720 10.1021/ar700217y
    • (2008) Acc. Chem. Res. , vol.41 , pp. 708-720
    • Thomas, J.M.1    Raja, R.2
  • 55
    • 9744268958 scopus 로고    scopus 로고
    • Chiral synthesis on catalysts immobilized in microporous and mesoporous materials
    • Li, C. Chiral synthesis on catalysts immobilized in microporous and mesoporous materials Catal. Rev.: Sci. Eng. 2004, 46, 419-492 10.1081/CR-200036734
    • (2004) Catal. Rev.: Sci. Eng. , vol.46 , pp. 419-492
    • Li, C.1
  • 56
    • 0033521191 scopus 로고    scopus 로고
    • Silica-supported tantalum catalysts for asymmetric epoxidations of allyl alcohols
    • Meunier, D.; Piechaczyk, A.; de Mallmann, A.; Basset, J.-M. Silica-supported tantalum catalysts for asymmetric epoxidations of allyl alcohols Angew. Chem., Int. Ed. 1999, 38, 3540-3542 10.1002/(SICI)1521-3773(19991203)38:23<3540::AID-ANIE3540>3.0.CO;2-U
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 3540-3542
    • Meunier, D.1    Piechaczyk, A.2    De Mallmann, A.3    Basset, J.-M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.