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Volumn 5, Issue 2, 2012, Pages 352-371

Homogeneous photocatalytic reactions with organometallic and coordination compounds-perspectives for sustainable chemistry

Author keywords

green chemistry; homogeneous catalysis; organic synthesis; photochemistry; transition metals

Indexed keywords

ACTIVATION ANALYSIS; BUTANE; BYPRODUCTS; CARBONYLATION; CATALYSIS; CHEMICAL COMPOUNDS; CHEMISTRY; ORGANOMETALLICS; PHOTOCHEMICAL REACTIONS; REACTION KINETICS; RUTHENIUM; RUTHENIUM COMPOUNDS; TRANSITION METALS;

EID: 84858683201     PISSN: 18645631     EISSN: 1864564X     Source Type: Journal    
DOI: 10.1002/cssc.201100286     Document Type: Review
Times cited : (109)

References (271)
  • 2
    • 84990162781 scopus 로고
    • Angew. Chem. Int. Ed. 1989, 28, 1193-1207.
    • (1989) Angew. Chem. Int. Ed. , vol.28 , pp. 1193-1207
  • 12
    • 53349090425 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 6322-6325.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6322-6325
  • 13
  • 15
    • 79251579273 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 1000-1045
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 1000-1045
  • 18
    • 84891566427 scopus 로고    scopus 로고
    • (Eds.: A. Albini, M. Fagnoni), Wiley-VCH, Weinheim
    • Handbook of Synthetic Photochemistry (Eds.:, A. Albini, M. Fagnoni,), Wiley-VCH, Weinheim, 2010.
    • (2010) Handbook of Synthetic Photochemistry
  • 38
  • 70
    • 4544286694 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 3795-3797.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3795-3797
  • 85
    • 51049114227 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 3188-3191.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3188-3191
  • 87
  • 88
  • 89
    • 0034595710 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1921-1923.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1921-1923
  • 92
  • 94
  • 98
    • 34548242588 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 6297-6300.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 6297-6300
  • 117
  • 122
    • 33746238143 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 3740-3747
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3740-3747
  • 124
    • 33746238148 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 3748-3759
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3748-3759
  • 126
    • 33746238145 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 3760-3765.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3760-3765
  • 150
    • 0003567644 scopus 로고
    • (Eds.: R. I. Ridgway, R. M. Silverstein, M. N. Inscoe), Marcel Dekker, New York
    • Behavior-Modifying Chemicals for Insect Management (Eds.:, R. I. Ridgway, R. M. Silverstein, M. N. Inscoe,), Marcel Dekker, New York, 1990
    • (1990) Behavior-Modifying Chemicals for Insect Management
  • 158
    • 70349924979 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6386-6389
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6386-6389
  • 163
  • 165
    • 85021025168 scopus 로고
    • Ph.D. Thesis, University of Bern (Switzerland)
    • For equipment conception, see: C. Weymuth, Ph.D. Thesis, University of Bern (Switzerland), 1989.
    • (1989)
    • Weymuth, C.1
  • 169
    • 33645836858 scopus 로고    scopus 로고
    • (Ed.: S. Schulz), Springer, Berlin, ; for reviews on the synthesis of pheromones see
    • W. Francke, K. Dettner, in Top. Curr. Chem., Vol. 240 (Ed.:, S. Schulz,), Springer, Berlin, 2005, pp. 85-166; for reviews on the synthesis of pheromones see
    • (2005) Top. Curr. Chem. , vol.240 , pp. 85-166
    • Francke, W.1    Dettner, K.2
  • 187
    • 72449185228 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9785-9789.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9785-9789
  • 191
    • 0004186505 scopus 로고
    • (Eds.: M. A. Fox, M. Chanon), Elsevier, Amsterdam
    • Photoinduced Electron Transfer (Eds.:, M. A. Fox, M. Chanon,), Elsevier, Amsterdam, 1988.
    • (1988) Photoinduced Electron Transfer
  • 197
    • 52149113820 scopus 로고    scopus 로고
    • for a typical recent example, see
    • D. W. C. MacMillan, Nature 2008, 455, 304-308; for a typical recent example, see
    • (2008) Nature , vol.455 , pp. 304-308
    • MacMillan, D.W.C.1
  • 209
    • 0032484067 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1998, 37, 3072-3082.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 3072-3082
  • 214
    • 77957332454 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 7274-7276.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 7274-7276
  • 217
    • 54749118228 scopus 로고    scopus 로고
    • For general remarks on organocatalytic enantioselective photoreactions, see
    • For general remarks on organocatalytic enantioselective photoreactions, see:, P. Wessig, Angew. Chem. 2006, 118, 2224-2227
    • (2006) Angew. Chem. , vol.118 , pp. 2224-2227
    • Wessig, P.1
  • 218
    • 33745333009 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 2168-2171.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2168-2171
  • 228
  • 229
    • 84890984520 scopus 로고    scopus 로고
    • (Ed.: L. Ackermann), Wiley-VCH, Weinheim
    • M. S. Viciu, S. P. Nolan, in Modern Arylation Methods (Ed.:, L. Ackermann,), Wiley-VCH, Weinheim, 2009, pp. 183-220.
    • (2009) Modern Arylation Methods , pp. 183-220
    • Viciu, M.S.1    Nolan, S.P.2
  • 233
    • 84891568337 scopus 로고    scopus 로고
    • (Ed.: J.-E. Bäckvall), Wiley-VCH, Weinheim
    • Modern Oxidation Methods (Ed.:, J.-E. Bäckvall,), Wiley-VCH, Weinheim, 2004.
    • (2004) Modern Oxidation Methods
  • 253
  • 254
  • 257
    • 84858682006 scopus 로고    scopus 로고
    • Special Issue: Activation of Unreactive Bonds for Organic Synthesis
    • Adv. Synth. Catal. 2003, 345, Issue 9-10: Special Issue: Activation of Unreactive Bonds for Organic Synthesis
    • (2003) Adv. Synth. Catal. , vol.345 , Issue.9-10
  • 258
    • 85021001904 scopus 로고    scopus 로고
    • Selective Functionalization of C-H Bonds
    • Chem. Rev. 2010, 110, Issue 2: Special Issue: Selective Functionalization of C-H Bonds.
    • (2010) Chem. Rev. , vol.110 , Issue.2
  • 261
    • 33744510833 scopus 로고    scopus 로고
    • For a discussion on the term "C-H Activation", see:, in (Ed.: G. Dyker), Wiley-VCH, Weinheim
    • For a discussion on the term "C-H Activation", see:, B. Sezen, D. Sames, in Handbook of C-H Transformations, Vol. 1 (Ed.:, G. Dyker,), Wiley-VCH, Weinheim, 2005, pp. 3-10.
    • (2005) Handbook of C-H Transformations, Vol. 1 , pp. 3-10
    • Sezen, B.1    Sames, D.2
  • 267
    • 0033571369 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 3391-3393.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 3391-3393
  • 269
    • 0011212021 scopus 로고
    • Through isomerization steps, the inner boryl function migrates to the end of an alkyl chain. Such an isomerization is also catalyzed by transition-metal complexes, see
    • Through isomerization steps, the inner boryl function migrates to the end of an alkyl chain. Such an isomerization is also catalyzed by transition-metal complexes, see:, D. A. Evans, A. R. Muci, R. Stürmer, J. Org. Chem. 1993, 58, 5307-5309.
    • (1993) J. Org. Chem. , vol.58 , pp. 5307-5309
    • Evans, D.A.1    Muci, A.R.2    Stürmer, R.3


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