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Volumn 6, Issue , 2010, Pages 1106-1119

Light-induced olefin metathesis

Author keywords

Catalysis; Light activation; Olefin metathesis; Photoactivation; Photoinitiation; Photoisomerisation; RCM; ROMP; Ruthenium; Tungsten

Indexed keywords


EID: 78751503006     PISSN: 18605397     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.6.127     Document Type: Review
Times cited : (66)

References (83)
  • 1
    • 36049015757 scopus 로고    scopus 로고
    • The remarkable metal-catalysed olefin metathesis reaction
    • DOI 10.1038/nature06351, PII NATURE06351
    • Hoveyda, A. H.; Zhugralin, A. R. Nature 2007, 450, 243-250. doi:10.1038/nature06351 (Pubitemid 350100555)
    • (2007) Nature , vol.450 , Issue.7167 , pp. 243-251
    • Hoveyda, A.H.1    Zhugralin, A.R.2
  • 3
    • 0344006321 scopus 로고    scopus 로고
    • doi:10.1002/1521-3773(20000901)39:17<3012::AID-ANIE3012>3.0.CO ;2-G
    • Fürstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012-3043. doi:10.1002/1521-3773(20000901)39:17<3012::AID-ANIE3012>3.0.CO ;2-G
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3012-3043
    • Fürstner, A.1
  • 6
    • 38949085170 scopus 로고    scopus 로고
    • In an attempt to provide a user's guide to the galaxy of benzylidene, alkoxybenzylidene, and indenylidene ruthenium olefin metathesis catalysts
    • DOI 10.1002/chem.200701340
    • Bieniek, M.; Michrowska, A.; Usanov, D. L.; Grela, K. Chem.-Eur. J. 2008, 14, 806-818. doi:10.1002/chem.200701340 (Pubitemid 351210563)
    • (2008) Chemistry - A European Journal , vol.14 , Issue.3 , pp. 806-818
    • Bieniek, M.1    Michrowska, A.2    Usanov, D.L.3    Grela, K.4
  • 7
    • 0034746687 scopus 로고    scopus 로고
    • 2RU=CHR olefin metathesis catalysts: An organometallic success story
    • DOI 10.1021/ar000114f
    • Trnka, T. M.; Grubbs, R. H. Acc. Chem. Res. 2001, 34, 18-29. doi:10.1021/ar000114f (Pubitemid 32093931)
    • (2001) Accounts of Chemical Research , vol.34 , Issue.1 , pp. 18-29
    • Trnka, T.M.1    Grubbs, R.H.2
  • 9
    • 77954817829 scopus 로고    scopus 로고
    • doi:10.1016/j.polymer.2010.05.002
    • Leitgeb, A.; Wappel, J.; Slugovc, C. Polymer 2010, 51, 2927-2946. doi:10.1016/j.polymer.2010.05.002
    • (2010) Polymer , vol.51 , pp. 2927-2946
    • Leitgeb, A.1    Wappel, J.2    Slugovc, C.3
  • 10
    • 33846709112 scopus 로고    scopus 로고
    • Living ring-opening metathesis polymerization
    • DOI 10.1016/j.progpolymsci.2006.08.006, PII S0079670006000736, 50 Years of Living Polymerization
    • Bielawski, C. W.; Grubbs, R. H. Prog. Polym. Sci. 2007, 32, 1-29. doi:10.1016/j.progpolymsci.2006.08.006 (Pubitemid 46198886)
    • (2007) Progress in Polymer Science (Oxford) , vol.32 , Issue.1 , pp. 1-29
    • Bielawski, C.W.1    Grubbs, R.H.2
  • 11
    • 1442360753 scopus 로고    scopus 로고
    • Wiley-VCH: Weinheim, Germany
    • Grubbs, R. H., Ed. Handbook of Metathesis; Wiley-VCH: Weinheim, Germany, 2003; Vol. 3.
    • (2003) Handbook of Metathesis , vol.3
    • Grubbs, R.H.1
  • 12
    • 1542316833 scopus 로고    scopus 로고
    • doi:10.1016/j.molcata.2003.10.049
    • Mol, J. C. J. Mol. Catal. A 2004, 213, 39-45. doi:10.1016/j.molcata.2003. 10.049
    • (2004) J. Mol. Catal. A , vol.213 , pp. 39-45
    • Mol, J.C.1
  • 16
    • 33846665005 scopus 로고    scopus 로고
    • doi:10.1002/adsc.200600484
    • Mori, M. Adv. Synth. Catal. 2007, 349, 121-135. doi:10.1002/adsc. 200600484
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 121-135
    • Mori, M.1
  • 19
    • 67649593583 scopus 로고    scopus 로고
    • Recent applications of alkene metathesis for fine chemical and supramolecular system synthesis
    • Imamoglu, Y.; Dragutan, V., Eds.; NATO Science Series II: Mathematics, Physics and Chemistry; Springer: Dordrecht, The Netherlands
    • Pozgan, F.; Dixneuf, P. H. Recent applications of alkene metathesis for fine chemical and supramolecular system synthesis.. In Metathesis Chemistry: From Nanostructure Design to Synthesis of Advanced Materials; Imamoglu, Y.; Dragutan, V., Eds.; NATO Science Series II: Mathematics, Physics and Chemistry, Vol. 243; Springer: Dordrecht, The Netherlands, 2007; pp 195-222.
    • (2007) Metathesis Chemistry: From Nanostructure Design to Synthesis of Advanced Materials , vol.243 , pp. 195-222
    • Pozgan, F.1    Dixneuf, P.H.2
  • 22
    • 0037157771 scopus 로고    scopus 로고
    • A solid-supported phosphine-free ruthenium alkylidene for olefin metathesis in methanol and water
    • DOI 10.1016/S0960-894X(02)00260-3, PII S0960894X02002603
    • Connon, S. J.; Blechert, S. Bioorg. Med. Chem. Lett. 2002, 12, 1873-1876. doi:10.1016/S0960-894X(02)00260-3 (Pubitemid 34680960)
    • (2002) Bioorganic and Medicinal Chemistry Letters , vol.12 , Issue.14 , pp. 1873-1876
    • Connon, S.J.1    Blechert, S.2
  • 23
    • 33746793185 scopus 로고    scopus 로고
    • New tunable catalysts for olefin metathesis: Controlling the initiation through electronic factors
    • DOI 10.1016/j.molcata.2005.12.049, PII S1381116906006522
    • Gulajski, L.; Michrowska, A.; Bujok, R.; Grela, K. J. Mol. Catal. A 2006, 254, 118-123. doi:10.1016/j.molcata.2005.12.049 (Pubitemid 44173024)
    • (2006) Journal of Molecular Catalysis A: Chemical , vol.254 , Issue.1-2 , pp. 118-123
    • Gulajski, L.1    Michrowska, A.2    Bujok, R.3    Grela, K.4
  • 24
    • 34447302076 scopus 로고    scopus 로고
    • Small-molecule N-heterocyclic-carbene-containing olefin-metathesis catalysts for use in water
    • DOI 10.1002/anie.200701258
    • Jordan, J. P.; Grubbs, R. H. Angew. Chem., Int. Ed. 2007, 46, 5152-5155. doi:10.1002/anie.200701258 (Pubitemid 47051277)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.27 , pp. 5152-5155
    • Jordan, J.P.1    Grubbs, R.H.2
  • 25
    • 33746823357 scopus 로고    scopus 로고
    • A green catalyst for green chemistry: Synthesis and application of an olefin metathesis catalyst bearing a quaternary ammonium group
    • DOI 10.1039/b605138c
    • Michrowska, A.; Gulajski, L.; Kaczmarska, Z.; Mennecke, K.; Kirschning, A.; Grela, K. Green Chem. 2006, 8, 685-688. doi:10.1039/b605138c (Pubitemid 44172611)
    • (2006) Green Chemistry , vol.8 , Issue.8 , pp. 685-688
    • Michrowska, A.1    Gulajski, L.2    Kaczmarska, Z.3    Mennecke, K.4    Kirschning, A.5    Grela, K.6
  • 27
    • 34247151186 scopus 로고    scopus 로고
    • Directed catalytic asymmetric olefin metathesis. Selectivity control by enoate and ynoate groups in Ru-catalyzed asymmetric ring-opening/cross- metathesis
    • DOI 10.1021/ja070187v
    • Giudici, R. E.; Hoveyda, A. H. J. Am. Chem. Soc. 2007, 129, 3824-3825. doi:10.1021/ja070187v (Pubitemid 46595494)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.13 , pp. 3824-3825
    • Giudici, R.E.1    Hoveyda, A.H.2
  • 30
    • 72249123161 scopus 로고    scopus 로고
    • doi:10.1021/jo9018649
    • Schmidt, B.; Staude, L. J. Org. Chem. 2009, 74, 9237-9240. doi:10.1021/jo9018649
    • (2009) J. Org. Chem. , vol.74 , pp. 9237-9240
    • Schmidt, B.1    Staude, L.2
  • 31
    • 61649124105 scopus 로고    scopus 로고
    • doi:10.2174/138527208786786264
    • Szadkowska, A.; Grela, K. Curr. Org. Chem. 2008, 12, 1631-1647. doi:10.2174/138527208786786264
    • (2008) Curr. Org. Chem. , vol.12 , pp. 1631-1647
    • Szadkowska, A.1    Grela, K.2
  • 49
    • 0024088303 scopus 로고
    • doi:10.1016/0304-5102(88)85127-7
    • Szymańska-Buzar, T. J. Mol. Catal. 1988, 48, 43-57. doi:10.1016/0304-5102(88)85127-7
    • (1988) J. Mol. Catal. , vol.48 , pp. 43-57
    • Szymańska-Buzar, T.1
  • 52
    • 0027376356 scopus 로고
    • doi:10.1016/S0040-4039(00)61746-X
    • Gita, B.; Sundararajan, G. Tetrahedron Lett. 1993, 34, 6123-6126. doi:10.1016/S0040-4039(00)61746-X
    • (1993) Tetrahedron Lett. , vol.34 , pp. 6123-6126
    • Gita, B.1    Sundararajan, G.2
  • 53
    • 0031017816 scopus 로고    scopus 로고
    • 4/hv - A new system for metathesis polymerisation
    • DOI 10.1016/S1381-1169(96)00085-4, PII S1381116996000854
    • Gita, B.; Sundararajan, G. J. Mol. Catal. A 1997, 79, 79-84. doi:10.1016/S1381-1169(96)00085-4 (Pubitemid 27054197)
    • (1997) Journal of Molecular Catalysis A: Chemical , vol.115 , Issue.1 , pp. 79-84
    • Gita, B.1    Sundararajan, G.2
  • 57
    • 33847086170 scopus 로고
    • doi:10.1021/ja00521a094
    • Katz, T. J.; Lee, S. J. J. Am. Chem. Soc. 1980, 102, 422-424.doi:10.1021/ ja00521a094
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 422-424
    • Katz, T.J.1    Lee, S.J.2
  • 60
    • 78751545166 scopus 로고    scopus 로고
    • The term 'latency' may lead to some controversy. We define a catalyst as latent when no appreciable reaction is observed for a given time period (i.e., 24 h) without an external stimulus (i.e., UV light) and noticeable product formation may be measured after the external stimulus is applied. See also reference [78]
    • The term 'latency' may lead to some controversy. We define a catalyst as latent when no appreciable reaction is observed for a given time period (i.e., 24 h) without an external stimulus (i.e., UV light) and noticeable product formation may be measured after the external stimulus is applied. See also reference [78].
  • 69
    • 0037973154 scopus 로고    scopus 로고
    • doi:10.1002/1615-4169(200208)344:6/7<749::AID-ADSC749>3.0.CO;2 -T
    • Delaude, L.; Szypa, M.; Demonceau, A.; Noels, A. F. Adv. Synth. Catal. 2002, 344, 749-756. doi:10.1002/1615-4169(200208)344:6/7<749::AID- ADSC749>3.0.CO;2 -T
    • (2002) Adv. Synth. Catal. , vol.344 , pp. 749-756
    • Delaude, L.1    Szypa, M.2    Demonceau, A.3    Noels, A.F.4
  • 81
    • 0021698945 scopus 로고
    • Applications of photoinitiators to the design of resists for semiconductor manufacturing
    • Davidson, T., Ed.; ACS Symposium Series; ACS Publications: Washington, U. S. A. doi:10.1021/bk-1984-0242.ch002
    • Ito, H.; Willson, C. G. Applications of Photoinitiators to the Design of Resists for Semiconductor Manufacturing. In Polymers in Electronics; Davidson, T., Ed.; ACS Symposium Series, Vol. 242; ACS Publications: Washington, U. S. A., 1984; pp 11-23. doi:10.1021/bk-1984-0242.ch002
    • (1984) Polymers in Electronics , vol.242 , pp. 11-23
    • Ito, H.1    Willson, C.G.2


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