메뉴 건너뛰기




Volumn 110, Issue 2, 2010, Pages 1082-1146

Transition metal-catalyzed direct arylation of substrates with activated sp3-hybridized C-H bonds and some of their synthetic equivalents with aryl halides and pseudohalides

Author keywords

[No Author keywords available]

Indexed keywords

ARYL HALIDES; ARYLATIONS; C-H BOND; CARBONYL COMPOUNDS; CATALYST SYSTEM; ELECTROPHILES; ENOL ETHERS; EXPERIMENTAL CONDITIONS; PSEUDO HALIDE; REGIOSELECTIVE SYNTHESIS; SILYL ENOL ETHERS; SIMPLE REACTION; SYNTHETIC EQUIVALENTS;

EID: 77349104061     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/cr9000836     Document Type: Article
Times cited : (836)

References (577)
  • 1
    • 33847802803 scopus 로고
    • For leading references, see: a
    • For leading references, see: (a) Morrell, D. C.; Kochi, J. K. J. Am. Chem. Soc. 1975, 97, 7262.
    • (1975) Am. Chem. Soc , vol.97 , pp. 7262
    • Morrell, D.C.1    Kochi, J.K.J.2
  • 9
    • 0033718962 scopus 로고    scopus 로고
    • Gagneur, S.; Montchamp, J.-L.; Negishi, E.-i Organometallics 2000, 19, 2417.
    • (i) Gagneur, S.; Montchamp, J.-L.; Negishi, E.-i Organometallics 2000, 19, 2417.
  • 26
    • 0342826097 scopus 로고
    • For leading references, see: a
    • For leading references, see: (a) Jones, P. R.; Young, J. R. J. Org. Chem. 1968, 33, 1675.
    • (1968) Org. Chem , vol.33 , pp. 1675
    • Jones, P.R.1    Young, J.R.J.2
  • 39
    • 77349113609 scopus 로고    scopus 로고
    • Ref 2h, c Ref 2i
    • (b) Ref 2h. (c) Ref 2i.
  • 52
    • 77349119892 scopus 로고    scopus 로고
    • Negishi, E.-i; Hu, Q.; Huang, Z.; Wang, G.; Yin, N. In The Chemistry of Organozinc Compounds; Rappoport, Z., Marek, I., Eds; Wiley-Interscience: New York, 2007; Chapter 11, p 457.
    • (l) Negishi, E.-i; Hu, Q.; Huang, Z.; Wang, G.; Yin, N. In The Chemistry of Organozinc Compounds; Rappoport, Z., Marek, I., Eds; Wiley-Interscience: New York, 2007; Chapter 11, p 457.
  • 53
    • 0032483724 scopus 로고    scopus 로고
    • For leading references, see: a
    • For leading references, see: (a) Giovannini, R.; Knochel, P. J. Am. Chem. Soc. 1998, 120, 11186.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 11186
    • Giovannini, R.1    Knochel, P.2
  • 57
    • 77349085162 scopus 로고    scopus 로고
    • Roberts, S. M, Ed, Wiley: Chichester, U.K
    • (e) Terao, J.; Kambe, N. Catalysts for Fine Chemicals; Roberts, S. M., Ed.; Wiley: Chichester, U.K., 2004; Vol. 3, p 128.
    • (2004) Catalysts for Fine Chemicals , vol.3 , pp. 128
    • Terao, J.1    Kambe, N.2
  • 60
    • 77349093864 scopus 로고    scopus 로고
    • Ref 51
    • (h) Ref 51.
  • 77
    • 12344251733 scopus 로고    scopus 로고
    • For reviews on transition metal-catalyzed cross-coupling reactions of unactivated alkyl halides and pseudohalides with organometallic compounds, see: (a) Netherton, M. R, Fu, G. C. Adv. Synth. Catal. 2004, 36, 1525
    • For reviews on transition metal-catalyzed cross-coupling reactions of unactivated alkyl halides and pseudohalides with organometallic compounds, see: (a) Netherton, M. R.; Fu, G. C. Adv. Synth. Catal. 2004, 36, 1525.
  • 96
    • 2942650166 scopus 로고    scopus 로고
    • For leading references, see: a
    • For leading references, see: (a) Baran, P. S.; Richter, J. M. J. Am. Chem. Soc. 2004, 126, 7450.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 7450
    • Baran, P.S.1    Richter, J.M.2
  • 109
    • 0040418708 scopus 로고
    • For a review on the nucleophilic coupling with arynes, see:, Trost, B. M, Fleming, I, Semmelhack, M. F, Eds, Pergamon Press: New York, Chapter 2.3
    • For a review on the nucleophilic coupling with arynes, see: Kessar, S. V. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Semmelhack, M. F., Eds.; Pergamon Press: New York, 1991; Vol. 4, Chapter 2.3.
    • (1991) Comprehensive Organic Synthesis , vol.4
    • Kessar, S.V.1
  • 117
    • 0000866608 scopus 로고
    • Trost, B. M, Fleming, I, Semmelhack, M. F, Eds, Pergamon Press: New York, Chapter 2.2
    • (h) Norris, R. K. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Semmelhack, M. F., Eds.; Pergamon Press: New York, 1991; Vol. 4,Chapter 2.2.
    • (1991) Comprehensive Organic Synthesis , vol.4
    • Norris, R.K.1
  • 120
  • 128
    • 0346265937 scopus 로고
    • McKillop, A, Ed, Pergamon Press: Oxford, U.K, Chapter 11 and references cited therein
    • (b) Pinhey, J. T. In Comprehensive Organometallic Chemistry II; McKillop, A., Ed.; Pergamon Press: Oxford, U.K., 1995; Vol. 11, Chapter 11 and references cited therein.
    • (1995) Comprehensive Organometallic Chemistry II , vol.11
    • Pinhey, J.T.1
  • 178
    • 0038645593 scopus 로고    scopus 로고
    • For a review on the synthesis and cross-coupling catalysis applications of polyethylene or polypropylene supported palladium complexes, see
    • (b) Churruca, F.; SanMartin, R.; Tellitu, I.; Domínguez, E. Tetrahedron Lett. 2003, 44, 5925. For a review on the synthesis and cross-coupling catalysis applications of polyethylene or polypropylene supported palladium complexes, see:
    • (2003) Tetrahedron Lett , vol.44 , pp. 5925
    • Churruca, F.1    SanMartin, R.2    Tellitu, I.3    Domínguez, E.4
  • 186
    • 0002893108 scopus 로고    scopus 로고
    • For reviews on N-heterocyclic carbenes (NHCs) and their applications in transition metal catalysis, see: (a) Weskamp, T.; Bohm, V. P. W.; Herrmann, W. A. J. Organomet. Chem. 2000, 600, 12.
    • For reviews on N-heterocyclic carbenes (NHCs) and their applications in transition metal catalysis, see: (a) Weskamp, T.; Bohm, V. P. W.; Herrmann, W. A. J. Organomet. Chem. 2000, 600, 12.
  • 196
  • 214
    • 0345982380 scopus 로고    scopus 로고
    • For recent reviews on the potential of palladacycles in synthesis, see: a
    • For recent reviews on the potential of palladacycles in synthesis, see: (a) Herrmann, W. A.; Böhm, V. P. W.; Reisinger, C.-P. J. Organomet. Chem. 1999, 576, 23.
    • (1999) J. Organomet. Chem , vol.576 , pp. 23
    • Herrmann, W.A.1    Böhm, V.P.W.2    Reisinger, C.-P.3
  • 226
    • 0035886138 scopus 로고    scopus 로고
    • For reviews on the reactivity and catalytic performances of metal complexes based on pincer framework, see: (a) Albrecht, M, van Koten, G. Angew. Chem, Int. Ed. 2001, 40, 3750
    • For reviews on the reactivity and catalytic performances of metal complexes based on pincer framework, see: (a) Albrecht, M.; van Koten, G. Angew. Chem., Int. Ed. 2001, 40, 3750.
  • 250
    • 0344064789 scopus 로고    scopus 로고
    • For reviews on the stereoselective construction of all-carbon quaternary centers, see: a
    • For reviews on the stereoselective construction of all-carbon quaternary centers, see: (a) Denissova, I.; Barriault, L. Tetrahedron 2003, 59, 10105.
    • (2003) Tetrahedron , vol.59 , pp. 10105
    • Denissova, I.1    Barriault, L.2
  • 256
    • 33750624379 scopus 로고    scopus 로고
    • For a review on the synthesis and applications of P-Phos, see
    • For a review on the synthesis and applications of P-Phos, see: Wu, J.; Chan, A. S. C. Acc. Chem. Res. 2006, 39, 711.
    • (2006) Acc. Chem. Res , vol.39 , pp. 711
    • Wu, J.1    Chan, A.S.C.2
  • 260
    • 0000296850 scopus 로고
    • For leading references on the regioselective synthesis of silyl enol ethers of ketones, see: a
    • For leading references on the regioselective synthesis of silyl enol ethers of ketones, see: (a) d' Angelo, J. Tetrahedron 1976, 32, 2979.
    • (1976) Tetrahedron , vol.32 , pp. 2979
    • d' Angelo, J.1
  • 271
    • 33751499126 scopus 로고    scopus 로고
    • For arylation reactions of silyl enol ethers of ketones with aryl electrophiles that do not involve Pd-catalysis, see: (a) Chen, K, Koser, G. F. J. Org. Chem. 1991, 56, 5764
    • For arylation reactions of silyl enol ethers of ketones with aryl electrophiles that do not involve Pd-catalysis, see: (a) Chen, K.; Koser, G. F. J. Org. Chem. 1991, 56, 5764.
  • 285
    • 84982459710 scopus 로고
    • For leading references on the synthesis of enol esters of ketones, see: a
    • For leading references on the synthesis of enol esters of ketones, see: (a) Hauthal, H. G.; Kluge, P.; Schmidt, H. J. Prakt. Chem. 1965, 29, 296.
    • (1965) J. Prakt. Chem , vol.29 , pp. 296
    • Hauthal, H.G.1    Kluge, P.2    Schmidt, H.3
  • 335
    • 21344491698 scopus 로고
    • For a review on the use of organotin enolates in organic synthesis, see: b
    • For a review on the use of organotin enolates in organic synthesis, see: (b) Shibata, I.; Baba, A. Org. Prep. Proced. Int. 1994, 26, 85.
    • (1994) Org. Prep. Proced. Int , vol.26 , pp. 85
    • Shibata, I.1    Baba, A.2
  • 339
    • 0036860845 scopus 로고    scopus 로고
    • For leading references on the Pd-catalyzed hydrodehalogenation reaction of aryl halides, see: a
    • For leading references on the Pd-catalyzed hydrodehalogenation reaction of aryl halides, see: (a) Alonso, F.; Beletskaya, I. P.; Yus, M. Chem. Rev. 2002, 102, 4009.
    • (2002) Chem. Rev , vol.102 , pp. 4009
    • Alonso, F.1    Beletskaya, I.P.2    Yus, M.3
  • 344
    • 77349116000 scopus 로고    scopus 로고
    • Caló, V, Nacci, A, Monopoli
    • (f) Caló, V.; Nacci, A.; Monopoli,
  • 345
    • 34548008341 scopus 로고    scopus 로고
    • A.; Damascelli, A.; leva, E.; Cioffi, N. J.Organomet. Chem. 2007, 692, 4397.
    • A.; Damascelli, A.; leva, E.; Cioffi, N. J.Organomet. Chem. 2007, 692, 4397.
  • 367
    • 84943913171 scopus 로고
    • For leading references on the synthesis of O-silyl ketene acetals, see: a
    • For leading references on the synthesis of O-silyl ketene acetals, see: (a) Rathke, M. W.; Sullivan, D. F. Synth. Commun. 1973, 3, 67.
    • (1973) Synth. Commun , vol.3 , pp. 67
    • Rathke, M.W.1    Sullivan, D.F.2
  • 403
    • 0003832495 scopus 로고
    • Zabicky, J, Ed, Wiley-Interscience: New York
    • (a) The Chemistry of Amides; Zabicky, J., Ed.; Wiley-Interscience: New York, 1970.
    • (1970) The Chemistry of Amides
  • 453
    • 15244362427 scopus 로고    scopus 로고
    • For a review up to 2004 on the developments of the Hurtley reaction, see: Beletskaya, I. P.; Sigeev, A. S.; Peregudov, A. S.; Petrovskii, E. V. J. Organomet. Chem. 2004, 689, 3810.
    • For a review up to 2004 on the developments of the Hurtley reaction, see: Beletskaya, I. P.; Sigeev, A. S.; Peregudov, A. S.; Petrovskii, E. V. J. Organomet. Chem. 2004, 689, 3810.
  • 459
    • 33947457556 scopus 로고
    • For noncatalytic procedures to prepare dialkyl arylmalonates, see: a
    • For noncatalytic procedures to prepare dialkyl arylmalonates, see: (a) Cope, A. C.; Field, L. J. Org. Chem. 1949, 14, 856.
    • (1949) J. Org. Chem , vol.14 , pp. 856
    • Cope, A.C.1    Field, L.2
  • 486
    • 0001285766 scopus 로고    scopus 로고
    • Uno, M.; S.; Seto, K.; Masuda, M.; Ueda, W.; Takahashi, S. Tetrahedron Lett. 1985, 26, 1553.
    • Uno, M.; S.; Seto, K.; Masuda, M.; Ueda, W.; Takahashi, S. Tetrahedron Lett. 1985, 26, 1553.
  • 492
    • 33846893890 scopus 로고    scopus 로고
    • For a recent review on carbon-carbon bond-forming reactions catalyzed by heterogeneous Pd catalysts, see: Yin, L, Liebscher, J. Chem. Rev. 2007, 107, 133
    • For a recent review on carbon-carbon bond-forming reactions catalyzed by heterogeneous Pd catalysts, see: Yin, L.; Liebscher, J. Chem. Rev. 2007, 107, 133.
  • 508
    • 0001017993 scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Johnson, C. R. Acc. Chem. Res. 1973, 6, 341.
    • (1973) Acc. Chem. Res , vol.6 , pp. 341
    • Johnson, C.R.1
  • 511
    • 0033985468 scopus 로고    scopus 로고
    • Reggelin, M.; Zur, C. Synthesis 2000, 1.
    • (d) Reggelin, M.; Zur, C. Synthesis 2000, 1.
  • 517
    • 0346339657 scopus 로고    scopus 로고
    • For a recent review on the Nef reaction, see
    • For a recent review on the Nef reaction, see: Ballini, R.; Petrini, M. Tetrahedron 2004, 60, 1017.
    • (2004) Tetrahedron , vol.60 , pp. 1017
    • Ballini, R.1    Petrini, M.2
  • 518
    • 0242526099 scopus 로고    scopus 로고
    • For reviews on this topic, see: a
    • For reviews on this topic, see: (a) Kachiuchi, K.; Chatani, N. Adv. Synth. Catal. 2003, 345, 1077.
    • (2003) Adv. Synth. Catal , vol.345 , pp. 1077
    • Kachiuchi, K.1    Chatani, N.2
  • 533
    • 33644544164 scopus 로고    scopus 로고
    • Daintith, J, Ed, Oxford University Press: Oxford, U.K
    • Dictionary of Chemistry; Daintith, J., Ed.; Oxford University Press: Oxford, U.K., 2000; p 61.
    • (2000) Dictionary of Chemistry , pp. 61
  • 534
    • 0034336016 scopus 로고    scopus 로고
    • For leading references on removal of palladium from reaction products, see: a
    • For leading references on removal of palladium from reaction products, see: (a) Ishihara, K.; Nakayama, M.; Kurihara, H.; Itoh, A.; Haraguchi, H. Chem. Lett. 2000, 29, 1218.
    • (2000) Chem. Lett , vol.29 , pp. 1218
    • Ishihara, K.1    Nakayama, M.2    Kurihara, H.3    Itoh, A.4    Haraguchi, H.5
  • 545
    • 0000560109 scopus 로고
    • For leading references on removal of copper from reaction mixtures and products, see: a
    • For leading references on removal of copper from reaction mixtures and products, see: (a) Neuberger, A.; Sanger, F. Biochem. J. 1943, 37, 515.
    • (1943) Biochem. J , vol.37 , pp. 515
    • Neuberger, A.1    Sanger, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.