메뉴 건너뛰기




Volumn 49, Issue 10, 2016, Pages 2232-2242

Decatungstate Anion for Photocatalyzed "window Ledge" Reactions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84991757107     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/acs.accounts.6b00339     Document Type: Article
Times cited : (273)

References (66)
  • 2
    • 84979164996 scopus 로고    scopus 로고
    • Early pioneers of organic photochemistry
    • König, B. Walter de Gruyter GmbH & Co. KG: Berlin
    • Schroll, P. P. Early pioneers of organic photochemistry. In Chemical Photocatalysis; König, B., Ed.; Walter de Gruyter GmbH & Co. KG: Berlin, 2013; pp 3-17.
    • (2013) Chemical Photocatalysis , pp. 3-17
    • Schroll, P.P.1
  • 4
    • 33947434924 scopus 로고
    • Reactions of Non-enolizable Ketones in Sunlight
    • Schönberg, A.; Mustafa, A. Reactions of Non-enolizable Ketones in Sunlight Chem. Rev. 1947, 40, 181-200 10.1021/cr60126a001
    • (1947) Chem. Rev. , vol.40 , pp. 181-200
    • Schönberg, A.1    Mustafa, A.2
  • 5
    • 77956384399 scopus 로고    scopus 로고
    • The greenest reagent in organic synthesis: Light
    • Tundo, P. Esposito, V. Eds; NATO Science for Peace and Security Series; Springer Science + Business Media B. V. Dordrecht, the Netherlands
    • Fagnoni, M.; Albini, A. The greenest reagent in organic synthesis: light. In Green Chemical Reactions, Tundo, P.; Esposito, V., Eds; NATO Science for Peace and Security Series; Springer Science + Business Media B. V.: Dordrecht, the Netherlands, 2008; pp 173-189.
    • (2008) Green Chemical Reactions , pp. 173-189
    • Fagnoni, M.1    Albini, A.2
  • 6
    • 84867642146 scopus 로고    scopus 로고
    • Photochemical reactions of aromatic compounds and the concept of the photon as a traceless reagent
    • Hoffmann, N. Photochemical reactions of aromatic compounds and the concept of the photon as a traceless reagent Photochem. Photobiol. Sci. 2012, 11, 1613-1643 10.1039/c2pp25074h
    • (2012) Photochem. Photobiol. Sci. , vol.11 , pp. 1613-1643
    • Hoffmann, N.1
  • 7
    • 1442326812 scopus 로고    scopus 로고
    • Green chemistry and photochemistry were born at the same time
    • Albini, A.; Fagnoni, M. Green chemistry and photochemistry were born at the same time Green Chem. 2004, 6, 1-6 10.1039/b309592d
    • (2004) Green Chem. , vol.6 , pp. 1-6
    • Albini, A.1    Fagnoni, M.2
  • 8
    • 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 10.1039/b909128a
    • (2009) Photochem. Photobiol. Sci. , vol.8 , pp. 1499-1516
    • Protti, S.1    Fagnoni, M.2
  • 9
    • 84922349899 scopus 로고    scopus 로고
    • Solar Photocatalysis: Materials, Reactors, some Commercial, and pre-Industrialized Applications. A Comprehensive Approach
    • Spasiano, D.; Marotta, R.; Malato, S.; Fernandez-Ibañez, P.; Di Somma, I. Solar Photocatalysis: Materials, Reactors, some Commercial, and pre-Industrialized Applications. A Comprehensive Approach Appl. Catal., B 2015, 170-171, 90-123 10.1016/j.apcatb.2014.12.050
    • (2015) Appl. Catal., B , vol.170-171 , pp. 90-123
    • Spasiano, D.1    Marotta, R.2    Malato, S.3    Fernandez-Ibañez, P.4    Di Somma, I.5
  • 10
    • 84987981750 scopus 로고    scopus 로고
    • Solar Photochemical Synthesis: From the Beginnings of Organic Photochemistry to the Solar Manufacturing of Commodity Chemicals
    • Oelgemöller, M. Solar Photochemical Synthesis: From the Beginnings of Organic Photochemistry to the Solar Manufacturing of Commodity Chemicals Chem. Rev. 2016, 116, 9664-9682
    • (2016) Chem. Rev. , vol.116 , pp. 9664-9682
    • Oelgemöller, M.1
  • 11
    • 70350061938 scopus 로고    scopus 로고
    • Synthesis of γ-lactols, γ-lactones and 1,4-monoprotected succinaldehydes under moderately concentrated sunlight
    • Dondi, D.; Protti, S.; Albini, A.; Carpio, S. M.; Fagnoni, M. Synthesis of γ-lactols, γ-lactones and 1,4-monoprotected succinaldehydes under moderately concentrated sunlight Green Chem. 2009, 11, 1653-1659 10.1039/b904427b
    • (2009) Green Chem. , vol.11 , pp. 1653-1659
    • Dondi, D.1    Protti, S.2    Albini, A.3    Carpio, S.M.4    Fagnoni, M.5
  • 12
    • 84896707663 scopus 로고    scopus 로고
    • Solar Synthesis: Prospects in Visible Light Photocatalysis
    • Schultz, D. M.; Yoon, T. P. Solar Synthesis: Prospects in Visible Light Photocatalysis Science 2014, 343, 1239176 10.1126/science.1239176
    • (2014) Science , vol.343 , pp. 1239176
    • Schultz, D.M.1    Yoon, T.P.2
  • 13
    • 34447108358 scopus 로고    scopus 로고
    • Photocatalysis for the formation of the C-C Bond
    • Fagnoni, M.; Dondi, D.; Ravelli, D.; Albini, A. Photocatalysis for the formation of the C-C Bond Chem. Rev. 2007, 107, 2725-2756 10.1021/cr068352x
    • (2007) Chem. Rev. , vol.107 , pp. 2725-2756
    • Fagnoni, M.1    Dondi, D.2    Ravelli, D.3    Albini, A.4
  • 14
    • 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 10.1039/B913880N
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 102-113
    • Narayanam, J.M.R.1    Stephenson, C.R.J.2
  • 15
    • 84880124916 scopus 로고    scopus 로고
    • Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
    • Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis Chem. Rev. 2013, 113, 5322-5363 10.1021/cr300503r
    • (2013) Chem. Rev. , vol.113 , pp. 5322-5363
    • Prier, C.K.1    Rankic, D.A.2    MacMillan, D.W.C.3
  • 16
    • 84904740263 scopus 로고    scopus 로고
    • Organic Synthetic Transformations Using Organic Dyes as Photoredox Catalysts
    • Fukuzumi, S.; Ohkubo, K. Organic Synthetic Transformations Using Organic Dyes as Photoredox Catalysts Org. Biomol. Chem. 2014, 12, 6059-6071 10.1039/C4OB00843J
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 6059-6071
    • Fukuzumi, S.1    Ohkubo, K.2
  • 17
    • 79955638859 scopus 로고    scopus 로고
    • Utilization of Natural Sunlight and Air in the Aerobic Oxidation of Benzyl Halides
    • Su, Y.; Zhang, L.; Jiao, N. Utilization of Natural Sunlight and Air in the Aerobic Oxidation of Benzyl Halides Org. Lett. 2011, 13, 2168-2171 10.1021/ol2002013
    • (2011) Org. Lett. , vol.13 , pp. 2168-2171
    • Su, Y.1    Zhang, L.2    Jiao, N.3
  • 18
    • 70350064068 scopus 로고    scopus 로고
    • Crossed Intermolecular [2 + 2] Cycloadditions of Acyclic Enones via Visible Light Photocatalysis
    • Du, J.; Yoon, T. P. Crossed Intermolecular [2 + 2] Cycloadditions of Acyclic Enones via Visible Light Photocatalysis J. Am. Chem. Soc. 2009, 131, 14604-14605 10.1021/ja903732v
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 14604-14605
    • Du, J.1    Yoon, T.P.2
  • 20
    • 84883189645 scopus 로고    scopus 로고
    • Photochemical activity of a key donor-acceptor complex can drive stereoselective catalytic α-alkylation of aldehydes
    • Arceo, E.; Jurberg, I. D.; álvarez-Fernández, A.; Melchiorre, P. Photochemical activity of a key donor-acceptor complex can drive stereoselective catalytic α-alkylation of aldehydes Nat. Chem. 2013, 5, 750-756 10.1038/nchem.1727
    • (2013) Nat. Chem. , vol.5 , pp. 750-756
    • Arceo, E.1    Jurberg, I.D.2    Álvarez-Fernández, A.3    Melchiorre, P.4
  • 21
    • 85027958369 scopus 로고    scopus 로고
    • Photocatalytic C-H Activation via Hydrogen Atom Transfer in Synthesis
    • Protti, S.; Fagnoni, M.; Ravelli, D. Photocatalytic C-H Activation via Hydrogen Atom Transfer in Synthesis ChemCatChem 2015, 7, 1516-1523 10.1002/cctc.201500125
    • (2015) ChemCatChem , vol.7 , pp. 1516-1523
    • Protti, S.1    Fagnoni, M.2    Ravelli, D.3
  • 23
    • 37049109818 scopus 로고
    • Solution photochemistry of tetrakis(tetrabutylammonium) decatungstate(VI) and catalytic hydrogen evolution from alcohols
    • Yamase, T.; Takabayashi, N.; Kaji, M. Solution photochemistry of tetrakis(tetrabutylammonium) decatungstate(VI) and catalytic hydrogen evolution from alcohols J. Chem. Soc., Dalton Trans. 1984, 793-799 10.1039/dt9840000793
    • (1984) J. Chem. Soc., Dalton Trans. , pp. 793-799
    • Yamase, T.1    Takabayashi, N.2    Kaji, M.3
  • 24
    • 85064715424 scopus 로고
    • Introduction of Functionality into Unactivated Carbon-Hydrogen Bonds. Catalytic Generation and Nonconventional Utilization of Organic Radicals
    • Hill, C. L. Introduction of Functionality into Unactivated Carbon-Hydrogen Bonds. Catalytic Generation and Nonconventional Utilization of Organic Radicals Synlett 1995, 1995, 127-132 10.1055/s-1995-4883
    • (1995) Synlett , vol.1995 , pp. 127-132
    • Hill, C.L.1
  • 25
    • 0000907858 scopus 로고
    • Excited states of polyoxometalates as oxidatively resistant initiators of hydrocarbon autoxidation. Selective production of hydroperoxides
    • Chambers, R. C.; Hill, C. L. Excited states of polyoxometalates as oxidatively resistant initiators of hydrocarbon autoxidation. Selective production of hydroperoxides Inorg. Chem. 1989, 28, 2509-2511 10.1021/ic00312a002
    • (1989) Inorg. Chem. , vol.28 , pp. 2509-2511
    • Chambers, R.C.1    Hill, C.L.2
  • 26
    • 0000336806 scopus 로고
    • Selective ethylation and vinylation of alkanes via polyoxotungstate photocatalyzed radical addition reactions
    • Jaynes, B. S.; Hill, C. L. Selective ethylation and vinylation of alkanes via polyoxotungstate photocatalyzed radical addition reactions J. Am. Chem. Soc. 1993, 115, 12212-12213 10.1021/ja00078a089
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 12212-12213
    • Jaynes, B.S.1    Hill, C.L.2
  • 27
    • 0001640858 scopus 로고
    • Radical Carbonylation of Alkanes via Polyoxotungstate Photocatalysis
    • Jaynes, B. S.; Hill, C. L. Radical Carbonylation of Alkanes via Polyoxotungstate Photocatalysis J. Am. Chem. Soc. 1995, 117, 4704-4705 10.1021/ja00121a028
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 4704-4705
    • Jaynes, B.S.1    Hill, C.L.2
  • 28
    • 0000068741 scopus 로고
    • Polyoxometalate systems for the catalytic selective production of nonthermodynamic alkenes from alkanes. Nature of excited-state deactivation processes and control of subsequent thermal processes in polyoxometalate photoredox chemistry
    • Renneke, R. F.; Pasquali, M.; Hill, C. L. Polyoxometalate systems for the catalytic selective production of nonthermodynamic alkenes from alkanes. Nature of excited-state deactivation processes and control of subsequent thermal processes in polyoxometalate photoredox chemistry J. Am. Chem. Soc. 1990, 112, 6585-6594 10.1021/ja00174a020
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6585-6594
    • Renneke, R.F.1    Pasquali, M.2    Hill, C.L.3
  • 29
    • 0000966189 scopus 로고
    • Roles of surface protonation on the photodynamic, catalytic, and other properties of polyoxometalates probed by the photochemical functionalization of alkanes. Implications for irradiated semiconductor metal oxides
    • Renneke, R. F.; Kadkhodayan, M.; Pasquali, M.; Hill, C. L. Roles of surface protonation on the photodynamic, catalytic, and other properties of polyoxometalates probed by the photochemical functionalization of alkanes. Implications for irradiated semiconductor metal oxides J. Am. Chem. Soc. 1991, 113, 8357-8367 10.1021/ja00022a024
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 8357-8367
    • Renneke, R.F.1    Kadkhodayan, M.2    Pasquali, M.3    Hill, C.L.4
  • 30
    • 0032275713 scopus 로고    scopus 로고
    • Decatungstate photocatalysis
    • Tanielian, C. Decatungstate photocatalysis Coord. Chem. Rev. 1998, 178-180, 1165-1181 10.1016/S0010-8545(98)00160-X
    • (1998) Coord. Chem. Rev. , vol.178-180 , pp. 1165-1181
    • Tanielian, C.1
  • 31
    • 33845471762 scopus 로고
    • Electrochemical and photochemical reduction of decatungstate: A reinvestigation
    • Chemseddine, A.; Sanchez, C.; Livage, J.; Launay, J. P.; Fournier, M. Electrochemical and photochemical reduction of decatungstate: a reinvestigation Inorg. Chem. 1984, 23, 2609-2613 10.1021/ic00185a014
    • (1984) Inorg. Chem. , vol.23 , pp. 2609-2613
    • Chemseddine, A.1    Sanchez, C.2    Livage, J.3    Launay, J.P.4    Fournier, M.5
  • 33
    • 5544315213 scopus 로고    scopus 로고
    • Kinetic and Mechanistic Aspects of Photocatalysis by Polyoxotungstates: A Laser Flash Photolysis, Pulse Radiolysis, and Continuous Photolysis Study
    • Tanielian, C.; Duffy, K.; Jones, A. Kinetic and Mechanistic Aspects of Photocatalysis by Polyoxotungstates: A Laser Flash Photolysis, Pulse Radiolysis, and Continuous Photolysis Study J. Phys. Chem. B 1997, 101, 4276-4282 10.1021/jp970475l
    • (1997) J. Phys. Chem. B , vol.101 , pp. 4276-4282
    • Tanielian, C.1    Duffy, K.2    Jones, A.3
  • 34
    • 37049087278 scopus 로고
    • 7- and electron-spin polarization of α-hydroxyalkyl radicals in the presence of alcohols
    • 7- and electron-spin polarization of α-hydroxyalkyl radicals in the presence of alcohols J. Chem. Soc., Dalton Trans. 1994, 2599-2608 10.1039/DT9940002599
    • (1994) J. Chem. Soc., Dalton Trans. , pp. 2599-2608
    • Yamase, T.1    Ohtaka, K.2
  • 35
    • 0001354430 scopus 로고    scopus 로고
    • On the nature of the charge-transfer transient in photocatalysis by the decatungstate anion
    • Duclusaud, H.; Borshch, S. A. On the nature of the charge-transfer transient in photocatalysis by the decatungstate anion Chem. Phys. Lett. 1998, 290, 526-534 10.1016/S0009-2614(98)00517-X
    • (1998) Chem. Phys. Lett. , vol.290 , pp. 526-534
    • Duclusaud, H.1    Borshch, S.A.2
  • 36
    • 0034653237 scopus 로고    scopus 로고
    • Reactivity of the charge transfer excited state of sodium decatungstate at the nanosecond time scale
    • Texier, I.; Delaire, J. A.; Giannotti, C. Reactivity of the charge transfer excited state of sodium decatungstate at the nanosecond time scale Phys. Chem. Chem. Phys. 2000, 2, 1205-1212 10.1039/a908588b
    • (2000) Phys. Chem. Chem. Phys. , vol.2 , pp. 1205-1212
    • Texier, I.1    Delaire, J.A.2    Giannotti, C.3
  • 37
    • 37049075803 scopus 로고
    • 4-, in acetonitrile and magnetic resonance studies of photoreduced species
    • 4-, in acetonitrile and magnetic resonance studies of photoreduced species J. Chem. Soc., Dalton Trans. 1988, 183-190 10.1039/DT9880000183
    • (1988) J. Chem. Soc., Dalton Trans. , pp. 183-190
    • Yamase, T.1    Usami, T.2
  • 38
    • 0000837043 scopus 로고
    • Photocatalytic Processes with Polyoxotungstates: Oxidation of Cyclohexylamine
    • Maldotti, A.; Amadelli, R.; Varani, G.; Tollari, S.; Porta, F. Photocatalytic Processes with Polyoxotungstates: Oxidation of Cyclohexylamine Inorg. Chem. 1994, 33, 2968-2973 10.1021/ic00091a041
    • (1994) Inorg. Chem. , vol.33 , pp. 2968-2973
    • Maldotti, A.1    Amadelli, R.2    Varani, G.3    Tollari, S.4    Porta, F.5
  • 40
    • 0000095344 scopus 로고    scopus 로고
    • Early Events in Decatungstate Photocatalyzed Oxidations: A Nanosecond Laser Transient Absorbance Reinvestigation
    • Duncan, D. C.; Fox, M. A. Early Events in Decatungstate Photocatalyzed Oxidations: A Nanosecond Laser Transient Absorbance Reinvestigation J. Phys. Chem. A 1998, 102, 4559-4567 10.1021/jp980723t
    • (1998) J. Phys. Chem. A , vol.102 , pp. 4559-4567
    • Duncan, D.C.1    Fox, M.A.2
  • 41
    • 0037468193 scopus 로고    scopus 로고
    • Decatungstate Photocatalyzed Electron-Transfer Reactions of Alkenes. Interception of the Geminate Radical Ion Pair by Oxygen
    • Tanielian, C.; Seghrouchni, R.; Schweitzer, C. Decatungstate Photocatalyzed Electron-Transfer Reactions of Alkenes. Interception of the Geminate Radical Ion Pair by Oxygen J. Phys. Chem. A 2003, 107, 1102-1111 10.1021/jp0217031
    • (2003) J. Phys. Chem. A , vol.107 , pp. 1102-1111
    • Tanielian, C.1    Seghrouchni, R.2    Schweitzer, C.3
  • 42
    • 80052029791 scopus 로고    scopus 로고
    • Predicting the UV spectrum of polyoxometalates by TD-DFT
    • Ravelli, D.; Dondi, D.; Fagnoni, M.; Albini, A.; Bagno, A. Predicting the UV spectrum of polyoxometalates by TD-DFT J. Comput. Chem. 2011, 32, 2983-2987 10.1002/jcc.21879
    • (2011) J. Comput. Chem. , vol.32 , pp. 2983-2987
    • Ravelli, D.1    Dondi, D.2    Fagnoni, M.3    Albini, A.4    Bagno, A.5
  • 44
    • 0000720940 scopus 로고    scopus 로고
    • Solar photodegradation of pesticides in water by sodium decatungstate
    • Texier, I.; Giannotti, C.; Malato, S.; Richter, C.; Delaire, J. Solar photodegradation of pesticides in water by sodium decatungstate Catal. Today 1999, 54, 297-307 10.1016/S0920-5861(99)00191-1
    • (1999) Catal. Today , vol.54 , pp. 297-307
    • Texier, I.1    Giannotti, C.2    Malato, S.3    Richter, C.4    Delaire, J.5
  • 45
    • 70349447447 scopus 로고    scopus 로고
    • Decatungstate as an Efficient Photocatalyst in Organic Chemistry
    • Tzirakis, M. D.; Lykakis, I. N.; Orfanopoulos, M. Decatungstate as an Efficient Photocatalyst in Organic Chemistry Chem. Soc. Rev. 2009, 38, 2609-2621 10.1039/b812100c
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2609-2621
    • Tzirakis, M.D.1    Lykakis, I.N.2    Orfanopoulos, M.3
  • 46
    • 84872573816 scopus 로고    scopus 로고
    • Photo-catalysis and Polyoxo-anion Decatungstate in Organic Chemistry: A Manifold Concept for Green Chemistry
    • Lykakis, I. N.; Evgenidou, E.; Orfanopoulos, M. Photo-catalysis and Polyoxo-anion Decatungstate in Organic Chemistry: A Manifold Concept for Green Chemistry Curr. Org. Chem. 2012, 16, 2400-2414 10.2174/138527212803520092
    • (2012) Curr. Org. Chem. , vol.16 , pp. 2400-2414
    • Lykakis, I.N.1    Evgenidou, E.2    Orfanopoulos, M.3
  • 47
    • 33745080899 scopus 로고    scopus 로고
    • Polyoxometallate photocatalysis for decontaminating the aquatic environment from organic and inorganic pollutants
    • Hiskia, A.; Troupis, A.; Antonaraki, S.; Gkika, E.; Papaconstantinou, P. K. E. Polyoxometallate photocatalysis for decontaminating the aquatic environment from organic and inorganic pollutants Int. J. Environ. Anal. Chem. 2006, 86, 233-242 10.1080/03067310500247520
    • (2006) Int. J. Environ. Anal. Chem. , vol.86 , pp. 233-242
    • Hiskia, A.1    Troupis, A.2    Antonaraki, S.3    Gkika, E.4    Papaconstantinou, P.K.E.5
  • 48
    • 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 10.1039/b917732a
    • (2009) Chem. Commun. , pp. 7351-7353
    • Protti, S.1    Ravelli, D.2    Fagnoni, M.3    Albini, A.4
  • 49
    • 84929190670 scopus 로고    scopus 로고
    • Photocatalyzed Site-selective C-H to C-C Conversion of Aliphatic Nitriles
    • Yamada, K.; Okada, M.; Fukuyama, T.; Ravelli, D.; Fagnoni, M.; Ryu, I. Photocatalyzed Site-selective C-H to C-C Conversion of Aliphatic Nitriles Org. Lett. 2015, 17, 1292-1295 10.1021/acs.orglett.5b00282
    • (2015) Org. Lett. , vol.17 , pp. 1292-1295
    • Yamada, K.1    Okada, M.2    Fukuyama, T.3    Ravelli, D.4    Fagnoni, M.5    Ryu, I.6
  • 50
    • 84901846293 scopus 로고    scopus 로고
    • Sunlight Photocatalyzed Regioselective β-Alkylation and Acylation of Cyclopentanones
    • Okada, M.; Fukuyama, T.; Yamada, K.; Ryu, I.; Ravelli, D.; Fagnoni, M. Sunlight Photocatalyzed Regioselective β-Alkylation and Acylation of Cyclopentanones Chem. Sci. 2014, 5, 2893-2898 10.1039/C4SC01072H
    • (2014) Chem. Sci. , vol.5 , pp. 2893-2898
    • Okada, M.1    Fukuyama, T.2    Yamada, K.3    Ryu, I.4    Ravelli, D.5    Fagnoni, M.6
  • 51
    • 84255162105 scopus 로고    scopus 로고
    • A Tin-Free Radical Photocatalyzed Addition to Vinyl Sulfones
    • Ravelli, D.; Montanaro, S.; Zema, M.; Fagnoni, M.; Albini, A. A Tin-Free Radical Photocatalyzed Addition to Vinyl Sulfones Adv. Synth. Catal. 2011, 353, 3295-3300 10.1002/adsc.201100591
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 3295-3300
    • Ravelli, D.1    Montanaro, S.2    Zema, M.3    Fagnoni, M.4    Albini, A.5
  • 52
    • 84908501183 scopus 로고    scopus 로고
    • Photocatalytic Synthesis of Oxetane Derivatives by Selective C-H Activation
    • Ravelli, D.; Zoccolillo, M.; Mella, M.; Fagnoni, M. Photocatalytic Synthesis of Oxetane Derivatives by Selective C-H Activation Adv. Synth. Catal. 2014, 356, 2781-2786 10.1002/adsc.201400027
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 2781-2786
    • Ravelli, D.1    Zoccolillo, M.2    Mella, M.3    Fagnoni, M.4
  • 53
    • 84877892034 scopus 로고    scopus 로고
    • Efficient C-H/C-N and C-H/C-CO-N Conversion via Decatungstate Photoinduced Alkylation of Diisopropyl Azodicarboxylate
    • Ryu, I.; Tani, A.; Fukuyama, T.; Ravelli, D.; Montanaro, S.; Fagnoni, M. Efficient C-H/C-N and C-H/C-CO-N Conversion via Decatungstate Photoinduced Alkylation of Diisopropyl Azodicarboxylate Org. Lett. 2013, 15, 2554-2557 10.1021/ol401061v
    • (2013) Org. Lett. , vol.15 , pp. 2554-2557
    • Ryu, I.1    Tani, A.2    Fukuyama, T.3    Ravelli, D.4    Montanaro, S.5    Fagnoni, M.6
  • 54
    • 78651254969 scopus 로고    scopus 로고
    • Smooth Photocatalytic Preparation of 2-Substituted-1,3-Benzodioxoles
    • Ravelli, D.; Albini, A.; Fagnoni, M. Smooth Photocatalytic Preparation of 2-Substituted-1,3-Benzodioxoles Chem.-Eur. J. 2011, 17, 572-579 10.1002/chem.201002546
    • (2011) Chem. - Eur. J. , vol.17 , pp. 572-579
    • Ravelli, D.1    Albini, A.2    Fagnoni, M.3
  • 56
    • 84895121802 scopus 로고    scopus 로고
    • Decatungstate Photocatalyzed Benzylation of Alkenes with Alkylaromatics
    • Qrareya, H.; Ravelli, D.; Fagnoni, M.; Albini, A. Decatungstate Photocatalyzed Benzylation of Alkenes with Alkylaromatics Adv. Synth. Catal. 2013, 355, 2891-2899 10.1002/adsc.201300598
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 2891-2899
    • Qrareya, H.1    Ravelli, D.2    Fagnoni, M.3    Albini, A.4
  • 57
    • 84944179714 scopus 로고    scopus 로고
    • Decatungstate Photocatalyzed Si-H/C-H Activation in Silyl Hydrides. Hydrosilylation of Electron-Poor Alkenes
    • Qrareya, H.; Dondi, D.; Ravelli, D.; Fagnoni, M. Decatungstate Photocatalyzed Si-H/C-H Activation in Silyl Hydrides. Hydrosilylation of Electron-Poor Alkenes ChemCatChem 2015, 7, 3350-3357 10.1002/cctc.201500562
    • (2015) ChemCatChem , vol.7 , pp. 3350-3357
    • Qrareya, H.1    Dondi, D.2    Ravelli, D.3    Fagnoni, M.4
  • 60
  • 63
    • 84894290025 scopus 로고    scopus 로고
    • Decatungstate incorporated metal-organic framework for degradation of rhodamine B under sunlight irradiation
    • Li, J.; Huang, Y.; Han, Q.-X. Decatungstate incorporated metal-organic framework for degradation of rhodamine B under sunlight irradiation Chin. J. Struc. Chem. 2013, 32, 1897-1903
    • (2013) Chin. J. Struc. Chem. , vol.32 , pp. 1897-1903
    • Li, J.1    Huang, Y.2    Han, Q.-X.3
  • 64
    • 84961626608 scopus 로고    scopus 로고
    • A photosensitizing decatungstate-based MOF as heterogeneous photocatalyst for the selective C-H alkylation of aliphatic nitriles
    • Shi, D.; He, C.; Sun, W.; Ming, Z.; Meng, C.; Duan, C. A photosensitizing decatungstate-based MOF as heterogeneous photocatalyst for the selective C-H alkylation of aliphatic nitriles Chem. Commun. 2016, 52, 4714-4717 10.1039/C6CC00862C
    • (2016) Chem. Commun. , vol.52 , pp. 4714-4717
    • Shi, D.1    He, C.2    Sun, W.3    Ming, Z.4    Meng, C.5    Duan, C.6
  • 65
    • 84964555867 scopus 로고    scopus 로고
    • Enantioselective catalytic construction of quaternary carbons by iminium ion trapping of photochemically generated radicals
    • Murphy, J. J.; Bastida, D.; Paria, S.; Fagnoni, M.; Melchiorre, P. Enantioselective catalytic construction of quaternary carbons by iminium ion trapping of photochemically generated radicals Nature 2016, 532, 218-222 10.1038/nature17438
    • (2016) Nature , vol.532 , pp. 218-222
    • Murphy, J.J.1    Bastida, D.2    Paria, S.3    Fagnoni, M.4    Melchiorre, P.5
  • 66
    • 84954384175 scopus 로고    scopus 로고
    • Decatungstate Photocatalyzed Acylations and Alkylations in Flow via Hydrogen Atom Transfer
    • Bonassi, F.; Ravelli, D.; Protti, S.; Fagnoni, M. Decatungstate Photocatalyzed Acylations and Alkylations in Flow via Hydrogen Atom Transfer Adv. Synth. Catal. 2015, 357, 3687-3695 10.1002/adsc.201500483
    • (2015) Adv. Synth. Catal. , vol.357 , pp. 3687-3695
    • Bonassi, F.1    Ravelli, D.2    Protti, S.3    Fagnoni, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.