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Volumn 17, Issue 21, 2013, Pages 2366-2373

Visible light photocatalysis. a green choice?

Author keywords

Atom economy; EATOS; Electron transfer; Green metrics; Photocatalysis; Process mass intensity; Ruthenium complexes; Visible light

Indexed keywords

RUTHENIUM COMPOUNDS;

EID: 84893206649     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/13852728113179990051     Document Type: Article
Times cited : (37)

References (57)
  • 1
    • 77953990194 scopus 로고    scopus 로고
    • Visible light photocatalysis as a greener approach to photochemical synthesis
    • Yoon, T. P.; Ischay, M. A.; Du, J. Visible light photocatalysis as a greener approach to photochemical synthesis. Nat. Chem., 2010, 2, 527-532.
    • (2010) Nat Chem , vol.2 , pp. 527-532
    • Yoon, T.P.1    Ischay, M.A.2    Du, J.3
  • 2
    • 78650383080 scopus 로고    scopus 로고
    • Visible light photoredox catalysis: Applications in organic synthesis
    • Narayanam, J. M. R.; Stephenson, C. R. J. Visible light photoredox catalysis: applications in organic synthesis. Chem. Soc. Rev., 2011, 40, 102-113.
    • (2011) Chem. Soc. Rev , vol.40 , pp. 102-113
    • Narayanam, J.M.R.1    Stephenson, C.R.J.2
  • 4
    • 84863643233 scopus 로고    scopus 로고
    • Visible-Light Photoredox Catalysis
    • Xuan, J.; Xiao, W.-J. Visible-Light Photoredox Catalysis. Angew. Chem. Int. Ed., 2012, 51, 6828-6838.
    • (2012) Angew Chem. Int. Ed , vol.51 , pp. 6828-6838
    • Xuan, J.1    Xiao, W.-J.2
  • 5
    • 84868372230 scopus 로고    scopus 로고
    • Photoredox functionalization of C-H bonds adjacent to a nitrogen atom
    • Shi, L.; Xia, W.-J. Photoredox functionalization of C-H bonds adjacent to a nitrogen atom. Chem. Soc. Rev., 2012, 41, 7687-7697.
    • (2012) Chem. Soc. Rev , vol.41 , pp. 7687-7697
    • Shi, L.1    Xia, W.-J.2
  • 7
    • 70449370334 scopus 로고    scopus 로고
    • The sunny side of chemistry: Green synthesis by solar light
    • Protti, S.; Fagnoni, M. The sunny side of chemistry: green synthesis by solar light. Photochem. Photobiol. Sci., 2009, 8, 1499-1516.
    • (2009) Photochem. Photobiol. Sci , vol.8 , pp. 1499-1516
    • Protti, S.1    Fagnoni, M.2
  • 8
    • 67650283342 scopus 로고    scopus 로고
    • Efficient Visible Light Photocatalysis of [2+2] Enone Cycloadditions
    • Ischay, M. A.; Anzovino, M. E.; Du, J.; Yoon, T. P. Efficient Visible Light Photocatalysis of [2+2] Enone Cycloadditions. J. Am. Chem. Soc., 2008, 130, 12886-12887.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 12886-12887
    • Ischay, M.A.1    Anzovino, M.E.2    Du, J.3    Yoon, T.P.4
  • 9
    • 79957532004 scopus 로고    scopus 로고
    • Visible light photocatalysis of radical anion hetero-Diels-Alder cycloadditions
    • Hurtley, A. E.; Cismesia, M. A.; Ischay, M. A.; Yoon, T. P. Visible light photocatalysis of radical anion hetero-Diels-Alder cycloadditions. Tetrahedron, 2011, 67, 4442-4448.
    • (2011) Tetrahedron , vol.67 , pp. 4442-4448
    • Hurtley, A.E.1    Cismesia, M.A.2    Ischay, M.A.3    Yoon, T.P.4
  • 10
    • 37049081303 scopus 로고
    • A New and Efficient Strategy for non-stabilized azomethineylide via photoinduced electron transfer (PET) initiated sequential double desilylation
    • Pandey, G.; Lakshmaiah, G.; Kumaraswamy, G. A New and Efficient Strategy for non-stabilized azomethineylide via photoinduced electron transfer (PET) initiated sequential double desilylation. J. Chem. Soc., Chem. Commun., 1992, 1313-1314.
    • (1992) J. Chem. Soc., Chem. Commun , pp. 1313-1314
    • Pandey, G.1    Lakshmaiah, G.2    Kumaraswamy, G.3
  • 11
    • 79551693079 scopus 로고    scopus 로고
    • 3+2 Cycloadditions of Aryl Cyclopropyl Ketones By Visible Light Photocatalysis
    • Lu, Z.; Shen, M.; Yoon, T. P. [3+2] Cycloadditions of Aryl Cyclopropyl Ketones by Visible Light Photocatalysis. J. Am. Chem. Soc., 2011, 133, 1162-1164.
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 1162-1164
    • Lu, Z.1    Shen, M.2    Yoon, T.P.3
  • 12
    • 84864453769 scopus 로고    scopus 로고
    • Crossed intermolecular [2+2] cycloaddition of styrenes by visible light photocatalysis
    • Ischay, M. A.; Ament, M. S.; Yoon, T. P. Crossed intermolecular [2+2] cycloaddition of styrenes by visible light photocatalysis. Chem. Sci., 2012, 3, 2807-2811.
    • (2012) Chem. Sci , vol.3 , pp. 2807-2811
    • Ischay, M.A.1    Ament, M.S.2    Yoon, T.P.3
  • 13
    • 84858635280 scopus 로고    scopus 로고
    • Endoperoxide Synthesis by Photocatalytic Aerobic [2+2+2] Cycloadditions
    • Parrish, J. D.; Ischay, M. A.; Lu, Z.; Guo, S.; Peters, N. R.; Yoon, T. P. Endoperoxide Synthesis by Photocatalytic Aerobic [2+2+2] Cycloadditions. Org. Lett., 2012, 14, 1640-1643.
    • (2012) Org Lett , vol.14 , pp. 1640-1643
    • Parrish, J.D.1    Ischay, M.A.2    Lu, Z.3    Guo, S.4    Peters, N.R.5    Yoon, T.P.6
  • 14
    • 53349122064 scopus 로고    scopus 로고
    • Merging Photoredox Catalysis with Organocatalysis: The Direct Asymmetric Alkylation of Aldehydes
    • Nicewicz, D. A.; MacMillan, D. W. C. Merging Photoredox Catalysis with Organocatalysis: The Direct Asymmetric Alkylation of Aldehydes. Science, 2008, 322, 77-80.
    • (2008) Science , vol.322 , pp. 77-80
    • Nicewicz, D.A.1    Macmillan, D.W.C.2
  • 15
    • 78751510344 scopus 로고    scopus 로고
    • Metal-Free, Cooperative Asymmetric Organophotoredox Catalysis with Visible Light
    • Neumann, M.; Fueldner, S.; Koenig, B.; Zeitler, K. Metal-Free, Cooperative Asymmetric Organophotoredox Catalysis with Visible Light. Angew. Chem. Int. Ed., 2011, 50, 951-954.
    • (2011) Angew. Chem. Int. Ed , vol.50 , pp. 951-954
    • Neumann, M.1    Fueldner, S.2    Koenig, B.3    Zeitler, K.4
  • 16
    • 84860449806 scopus 로고    scopus 로고
    • Visible light photoredox organocatalysis: A fully transition metalfree direct asymmetric -alkylation of aldehydes
    • Fidaly, K.; Ceballos, C.; Falguières, A.; Sylla-Iyarreta Veitia, M.; Guy, A.; Ferroud, C. Visible light photoredox organocatalysis: a fully transition metalfree direct asymmetric -alkylation of aldehydes. Green Chem., 2012, 14, 1293-1297.
    • (2012) Green Chem , vol.14 , pp. 1293-1297
    • Fidaly, K.1    Ceballos, C.2    Falguières, A.3    Sylla-Iyarreta, V.M.4    Guy, A.5    Ferroud, C.6
  • 17
    • 77957304088 scopus 로고    scopus 로고
    • Enantioselective -benzylation of Aldehydes via Photoredox Organocatalysis
    • Shih, H.-W.; Vander Wal, M. N.; Grange, R. L.; MacMillan, D. W. C., Enantioselective -benzylation of Aldehydes via Photoredox Organocatalysis. J. Am. Chem. Soc., 2010, 132, 13600-13603.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 13600-13603
    • Shih, H.-W.1    Vander, W.M.N.2    Grange, R.L.3    Macmillan, D.W.C.4
  • 18
    • 84869189955 scopus 로고    scopus 로고
    • Visible-Light-Mediated -Arylation of Enol Acetates Using Aryl Diazonium Salts
    • Hering, T.; Hari, D. P.; Koenig, B. Visible-Light-Mediated -Arylation of Enol Acetates Using Aryl Diazonium Salts. J. Org. Chem., 2012, 77, 10347-10352.
    • (2012) J. Org. Chem , vol.77 , pp. 10347-10352
    • Hering, T.1    Hari, D.P.2    Koenig, B.3
  • 19
    • 68249144236 scopus 로고    scopus 로고
    • Enantioselective -trifluoromethylation of Aldehydes via Photoredox Organocatalysis
    • Nagib, D. A.; Scott, M. E.; MacMillan, D. W. C. Enantioselective -trifluoromethylation of Aldehydes via Photoredox Organocatalysis. J. Am. Chem. Soc., 2009, 131, 10875-10877.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 10875-10877
    • Nagib, D.A.1    Scott, M.E.2    Macmillan, D.W.C.3
  • 21
    • 0001414633 scopus 로고
    • Photochemical and Chemical Enzyme Catalyzed Debromination of meso-1,2-Dibromostilbene in Multiphase Systems
    • Maidan, R.; Willner, I. Photochemical and Chemical Enzyme Catalyzed Debromination of meso-1,2-Dibromostilbene in Multiphase Systems. J. Am. Chem. Soc., 1986, 108, 1080-1082.
    • (1986) J. Am. Chem. Soc , vol.108 , pp. 1080-1082
    • Maidan, R.1    Willner, I.2
  • 22
    • 67649625293 scopus 로고    scopus 로고
    • Electron-Transfer Photoredox Catalysis: Development of a Tin-Free Reductive Dehalogenation Reaction
    • Narayanam, J. M. R.; Tucker, J. W.; Stephenson, C. R. J. Electron-Transfer Photoredox Catalysis: Development of a Tin-Free Reductive Dehalogenation Reaction. J. Am. Chem. Soc., 2009, 131, 8756-8757.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 8756-8757
    • Narayanam, J.M.R.1    Tucker, J.W.2    Stephenson, C.R.J.3
  • 23
    • 84856823966 scopus 로고    scopus 로고
    • Metal-Free, Visible-Light-Mediated Direct C-H Arylation of Heteroarenes with Aryl Diazonium Salts
    • Hari, D. P.; Schroll, P.; Koenig, B. Metal-Free, Visible-Light-Mediated Direct C-H Arylation of Heteroarenes with Aryl Diazonium Salts. J. Am. Chem. Soc., 2012, 134, 2958-2961.
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 2958-2961
    • Hari, D.P.1    Schroll, P.2    Koenig, B.3
  • 24
    • 84867719861 scopus 로고    scopus 로고
    • Photocatalytic Arylation of Alkenes, Alkynes and Enones with Diazonium Salts
    • Schroll, P.; Hari, D. P.; Koenig, B. Photocatalytic Arylation of Alkenes, Alkynes and Enones with Diazonium Salts. ChemistryOpen, 2012, 1, 130-133.
    • (2012) ChemistryOpen , vol.1
    • Schroll, P.1    Hari, D.P.2    Koenig, B.3
  • 25
    • 84874616023 scopus 로고    scopus 로고
    • Transition Metal Photoredox Catalysis of Radical Thiol-Ene Reactions
    • Tyson, E. L.; Ament, M. S.; Yoon, T. P. Transition Metal Photoredox Catalysis of Radical Thiol-Ene Reactions. J. Org. Chem., 2013, 78, 2046-2050.
    • (2013) J. Org. Chem , vol.78 , pp. 2046-2050
    • Tyson, E.L.1    Ament, M.S.2    Yoon, T.P.3
  • 26
    • 37049113623 scopus 로고
    • Photocatalysis of the Pschorr reaction by tris (2,2 bipyridyl)ruthenium(II) in the phenanthrene series
    • Cano-Yelo, H.; Deronzier, A. Photocatalysis of the Pschorr reaction by tris (2,2 bipyridyl)ruthenium(II) in the phenanthrene series. J. Chem. Soc., Perkin Trans. 2, 1984, 1093-1098.
    • (1984) J. Chem. Soc., Perkin Trans , vol.2 , pp. 1093-1098
    • Cano-Yelo, H.1    Deronzier, A.2
  • 27
    • 84862174339 scopus 로고    scopus 로고
    • Synthesis of symmetric anhydrides using visible light-mediated photoredox catalysis
    • Konieczynska, M. D.; Dai, C.; Stephenson, C. R. J. Synthesis of symmetric anhydrides using visible light-mediated photoredox catalysis. Org. Biomol. Chem., 2012, 10, 4509-4511.
    • (2012) Org. Biomol. Chem , vol.10 , pp. 4509-4511
    • Konieczynska, M.D.1    Dai, C.2    Stephenson, C.R.J.3
  • 28
  • 29
    • 79959576121 scopus 로고    scopus 로고
    • Visible-LightInduced Metal-Free Allylic Oxidation Utilizing a Coupled Photocatalytic System of g-C3N4 and N-Hydroxy Compounds
    • Zhang, P.; Wang, Y.; Yao, J.; Wang, C.; Yan, C.; Antonietti, M.; Li, H.; Visible-LightInduced Metal-Free Allylic Oxidation Utilizing a Coupled Photocatalytic System of g-C3N4 and N-Hydroxy Compounds. Adv. Synth. Catal., 2011, 353, 1447-1451.
    • (2011) Adv. Synth. Catal , vol.353 , pp. 1447-1451
    • Zhang, P.1    Wang, Y.2    Yao, J.3    Wang, C.4    Yan, C.5    Antonietti, M.6    Li, H.7
  • 31
    • 84871659735 scopus 로고    scopus 로고
    • Organic Dye-Photocatalyzed Acylnitroso Ene Reaction
    • Teo, Y. C.; Pan, Y.; Tan, C. H. Organic Dye-Photocatalyzed Acylnitroso Ene Reaction. Chem. Cat. Chem., 2013, 5, 235-240.
    • (2013) Chem. Cat. Chem , vol.5 , pp. 235-240
    • Teo, Y.C.1    Pan, Y.2    Tan, C.H.3
  • 32
    • 79251610017 scopus 로고    scopus 로고
    • Visible-light-mediated conversion of alcohols to halides
    • Dai, C.; Narayanam, J. M. R.; Stephenson, C. R. J. Visible-light-mediated conversion of alcohols to halides. Nat. Chem., 2011, 3, 140-145.
    • (2011) Nat. Chem , vol.3 , pp. 140-145
    • Dai, C.1    Narayanam, J.M.R.2    Stephenson, C.R.J.3
  • 33
    • 79953067379 scopus 로고    scopus 로고
    • Intermolecular Atom Transfer Radical Addition to Olefins Mediated by Oxidative Quenching of Photoredox Catalysts
    • Nguyen, J. D.; Tucker, J. W.; Konieczynska, M. D.; Stephenson, C. R. J. Intermolecular Atom Transfer Radical Addition to Olefins Mediated by Oxidative Quenching of Photoredox Catalysts. J. Am. Chem. Soc., 2011, 133, 4160-4163.
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 4160-4163
    • Nguyen, J.D.1    Tucker, J.W.2    Konieczynska, M.D.3    Stephenson, C.R.J.4
  • 34
    • 84861837106 scopus 로고    scopus 로고
    • Cu(dap)2Cl As an Efficient Visible-Light-Driven Photoredox Catalyst in Carbon-Carbon Bond- Forming Reactions
    • Pirtsch, M.; Paria, S.; Matsuno, T.; Isobe, H.; Reiser, O. [Cu(dap)2Cl] As an Efficient Visible-Light-Driven Photoredox Catalyst in Carbon-Carbon Bond- Forming Reactions. Chem. Eur. J., 2012, 18, 7336-7340.
    • (2012) Chem. Eur. J , vol.18 , pp. 7336-7340
    • Pirtsch, M.1    Paria, S.2    Matsuno, T.3    Isobe, H.4    Reiser, O.5
  • 35
    • 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
  • 36
    • 84856707069 scopus 로고    scopus 로고
    • Visible Light Photoredox Catalysis: Generation and Addition of N-Aryltetrahydroisoquinoline-Derived amino Radicals to Michael Acceptors
    • Kohls, P.; Jadhav, D.; Pandey, G.; Reiser, O. Visible Light Photoredox Catalysis: Generation and Addition of N-Aryltetrahydroisoquinoline-Derived amino Radicals to Michael Acceptors. Org. Lett., 2012, 14, 672-675.
    • (2012) Org. Lett , vol.14 , pp. 672-675
    • Kohls, P.1    Jadhav, D.2    Pandey, G.3    Reiser, O.4
  • 37
    • 79960492760 scopus 로고    scopus 로고
    • Using the Right Green Yardstick: Why Process Mass Intensity Is Used in the Pharmaceutical Industry To Drive More Sustainable Processes
    • Jimenez-Gonzalez, C.; Ponder, C. S.; Broxterman, Q. B.; Manley, J. B. Using the Right Green Yardstick: Why Process Mass Intensity Is Used in the Pharmaceutical Industry To Drive More Sustainable Processes. Org. Process Res. Dev., 2011, 15, 912-917.
    • (2011) Org. Process Res. Dev , vol.15 , pp. 912-917
    • Jimenez-Gonzalez, C.1    Ponder, C.S.2    Broxterman, Q.B.3    Manley, J.B.4
  • 38
    • 36348937198 scopus 로고    scopus 로고
    • The E Factor: Fifteen years on
    • Sheldon, R. A. The E Factor: fifteen years on. Green Chem., 2007, 9, 1273-1283.
    • (2007) Green Chem , vol.9 , pp. 1273-1283
    • Sheldon, R.A.1
  • 39
    • 0037119280 scopus 로고    scopus 로고
    • Environmental Performance Metrics for Daily Use in Synthetic Chemistry
    • Eissen, M.; Metzger, J. O. Environmental Performance Metrics for Daily Use in Synthetic Chemistry. Chem. Eur. J., 2002, 8, 3580-3585.
    • (2002) Chem. Eur. J , vol.8 , pp. 3580-3585
    • Eissen, M.1    Metzger, J.O.2
  • 40
    • 36048964631 scopus 로고    scopus 로고
    • Photochemistry in synthesis: Where, when, and why
    • Protti, S.; Dondi, D.; Fagnoni, M.; Albini, A. Photochemistry in synthesis: Where, when, and why. Pure Appl. Chem., 2007, 79, 1929-1938.
    • (2007) Pure Appl. Chem , vol.79 , pp. 1929-1938
    • Protti, S.1    Dondi, D.2    Fagnoni, M.3    Albini, A.4
  • 41
    • 67649439162 scopus 로고    scopus 로고
    • Assessing photochemistry as a green synthetic method. Carbon-carbon bond forming reactions
    • Protti, S.; Dondi, D.; Fagnoni, M.; Albini, A. Assessing photochemistry as a green synthetic method. Carbon-carbon bond forming reactions. Green Chem., 2009, 11, 239-249.
    • (2009) Green Chem , vol.11 , pp. 239-249
    • Protti, S.1    Dondi, D.2    Fagnoni, M.3    Albini, A.4
  • 42
    • 0035082593 scopus 로고    scopus 로고
    • A Convenient Method for Synthesis of Symmetrical Acid Anhydrides from Carboxylic Acids with Trichloroacetonitrile and Triphenylphosphine
    • Kim, J.; Jang, D. O. A Convenient Method for Synthesis of Symmetrical Acid Anhydrides from Carboxylic Acids with Trichloroacetonitrile and Triphenylphosphine. Synthetic Commun., 2001, 31, 395-399.
    • (2001) Synthetic Commun , vol.31 , pp. 395-399
    • Kim, J.1    Jang, D.O.2
  • 43
    • 77950854848 scopus 로고    scopus 로고
    • The Productive Merger of Iodonium Salts and Organocatalysis: A Non-photolytic Approach to the Enantioselective trifluoromethylation of Aldehydes
    • Allen, A. E.; MacMillan, D. W. C. The Productive Merger of Iodonium Salts and Organocatalysis: A Non-photolytic Approach to the Enantioselective trifluoromethylation of Aldehydes. J. Am. Chem. Soc., 2010, 132, 4986-4987.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 4986-4987
    • Allen, A.E.1    Macmillan, D.W.C.2
  • 45
    • 66449105546 scopus 로고    scopus 로고
    • Oxidative coupling of amines and ketones by combined vanadium and organocatalysis
    • Sud, A.; Sureshkumarz, D.; Klussmann, M. Oxidative coupling of amines and ketones by combined vanadium and organocatalysis. Chem. Commun., 2009, 3169-3171.
    • (2009) Chem. Commun , pp. 3169-3171
    • Sud, A.1    Sureshkumarz, D.2    Klussmann, M.3
  • 46
    • 77952733318 scopus 로고    scopus 로고
    • Heterogeneously Catalyzed Oxidative Cyanation of Tertiary Amines with Sodium Cyanide/Hydrogen Peroxide using Polymer-Supported Iron(II) Phthalocyanines as Catalyst
    • Singhal, S.; Jain, S. L.; Saina, B. Heterogeneously Catalyzed Oxidative Cyanation of Tertiary Amines with Sodium Cyanide/Hydrogen Peroxide using Polymer-Supported Iron(II) Phthalocyanines as Catalyst. Adv. Synth. Catal., 2010, 352, 1338-1344.
    • (2010) Adv. Synth. Catal , vol.352 , pp. 1338-1344
    • Singhal, S.1    Jain, S.L.2    Saina, B.3
  • 47
    • 80055094770 scopus 로고    scopus 로고
    • Solvent-Free Cross-Dehydrogenative Coupling Reactions under High Speed Ball-Milling Conditions Applied to the Synthesis of Functionalized Tetrahydroisoquinolines
    • Su, W.; Yu, J.; Li, Z.; Jiang, Z. Solvent-Free Cross-Dehydrogenative Coupling Reactions under High Speed Ball-Milling Conditions Applied to the Synthesis of Functionalized Tetrahydroisoquinolines. J. Org. Chem., 2011, 76, 9144-9150.
    • (2011) J. Org. Chem , vol.76 , pp. 9144-9150
    • Su, W.1    Yu, J.2    Li, Z.3    Jiang, Z.4
  • 48
    • 77954725849 scopus 로고    scopus 로고
    • Aerobic and Electrochemical Oxidative CrossDehydrogenative-Coupling
    • Olivier Basl, O.; Borduas, N.; Dubois, P.; Chapuzet, J. M.; Chan, T.-H.; Lessard, J.; Li, C.-J. Aerobic and Electrochemical Oxidative CrossDehydrogenative-Coupling (CDC) Reaction in an Imidazolium-Based Ionic Liquid. Chem. Eur. J., 2010, 16, 8162-8166.
    • (2010) Chem. Eur. J , vol.16 , pp. 8162-8166
    • Olivier, B.O.1    Borduas, N.2    Dubois, P.3    Chapuzet, J.M.4    Chan, T.-H.5    Lessard, J.6    Li, C.-J.7
  • 50
    • 79751515504 scopus 로고    scopus 로고
    • Dual catalysis: Combining photoredox and Lewis base catalysis for direct Mannich reactions
    • Rueping, M. Vila, C. M.; Koenigs, R. M., Poscharny, K.; Fabry, D. C. Dual catalysis: combining photoredox and Lewis base catalysis for direct Mannich reactions. Chem. Commun., 2011, 47, 2360-2362.
    • (2011) Chem. Commun , vol.47 , pp. 2360-2362
    • Rueping, M.1    Vila, C.M.2    Koenigs, R.M.3    Poscharny, K.4    Fabry, D.C.5
  • 51
    • 84859029745 scopus 로고    scopus 로고
    • Light-Mediated Heterogeneous Cross Dehydrogenative Coupling Reactions: Metal Oxides as Efficient, Recyclable, Photoredox Catalysts in C-C Bond-Forming Reactions
    • Rueping, M.; Zoller, J.; Fabry, D. C.; Poscharny, K.; Koenigs, R. M.; Weirich, T. E.; Mayer, J. Light-Mediated Heterogeneous Cross Dehydrogenative Coupling Reactions: Metal Oxides as Efficient, Recyclable, Photoredox Catalysts in C-C Bond-Forming Reactions. Chem. Eur. J., 2012, 18, 3478-3481.
    • (2012) Chem. Eur. J , vol.18
    • Rueping, M.1    Zoller, J.2    Fabry, D.C.3    Poscharny, K.4    Koenigs, R.M.5    Weirich, T.E.6    Mayer, J.7
  • 52
    • 80053531171 scopus 로고    scopus 로고
    • Dehydrogenative coupling reactions catalysed by Rose Bengal using visible light irradiation
    • Pan, Y.; Kee, C. W.; Chen, L.; Tan, C.-H. Dehydrogenative coupling reactions catalysed by Rose Bengal using visible light irradiation. Green Chem., 2011, 13, 2682-2685.
    • (2011) Green Chem , vol.13 , pp. 2682-2685
    • Pan, Y.1    Kee, C.W.2    Chen, L.3    Tan, C.-H.4
  • 53
    • 79960275849 scopus 로고    scopus 로고
    • Photochemical technologies assessed: The case of rose oxide
    • Ravelli, D.; Protti, S.; Neri, P.; Fagnoni, M.; Albini, A. Photochemical technologies assessed: the case of rose oxide. Green Chem., 2011, 13, 1876-1884.
    • (2011) Green Chem , vol.13 , pp. 1876-1884
    • Ravelli, D.1    Protti, S.2    Neri, P.3    Fagnoni, M.4    Albini, A.5
  • 54
    • 85195238602 scopus 로고    scopus 로고
    • For details on the, topic, see
    • For details on the Energy-induced Methane Equivalents topic, see: http://www.oc-praktikum.de/en/articles/pdf/EnergyIndices_en.pdf.
    • Energy-induced Methane Equivalents
  • 55
    • 72649100132 scopus 로고    scopus 로고
    • Solar Light-driven Photocatalyzed Alkylations. Chemistry on the Window Ledge
    • Protti, S.; Ravelli, D.; Fagnoni, M.; Albini, A. Solar Light-driven Photocatalyzed Alkylations. Chemistry on the Window Ledge. Chem. Commun., 2009, 7351-7353.
    • (2009) Chem. Commun , pp. 7351-7353
    • Protti, S.1    Ravelli, D.2    Fagnoni, M.3    Albini, A.4
  • 56
    • 84861827411 scopus 로고    scopus 로고
    • Application of Microflow Conditions to Visible Light Photoredox Catalysis
    • Neumann, M.; Zeitler, K. Application of Microflow Conditions to Visible Light Photoredox Catalysis. Org. Lett., 2012, 14, 2658-2661.
    • (2012) Org Lett , vol.14 , pp. 2658-2661
    • Neumann, M.1    Zeitler, K.2
  • 57
    • 84859949266 scopus 로고    scopus 로고
    • A Photoflow Reactor for the Continuous Photoredox-Mediated Synthesis of C-Glycoamino Acids and CGlycolipids
    • Andrews, R. S.; Becker, J. J.; Gagné, M. R. A Photoflow Reactor for the Continuous Photoredox-Mediated Synthesis of C-Glycoamino Acids and CGlycolipids, Angew. Chem. Int. Ed., 2012, 51, 4140-4143.
    • (2012) Angew. Chem. Int. Ed , vol.51 , pp. 4140-4143
    • Andrews, R.S.1    Becker, J.J.2    Gagné, M.R.3


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