메뉴 건너뛰기




Volumn , Issue 16, 2010, Pages 2999-3025

When organocatalysis meets transition-metal catalysis

Author keywords

Asymmetric catalysis; Dual catalysis; Organocatalysis; Transition metals; Transition metal catalysis

Indexed keywords


EID: 77952637874     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000004     Document Type: Review
Times cited : (558)

References (227)
  • 9
    • 77952612176 scopus 로고    scopus 로고
    • In more than 3100 article topics based on the scifinder survey, until December 20, 2009
    • In more than 3100 article topics based on the scifinder survey, until December 20, 2009.
  • 11
    • 34250627489 scopus 로고    scopus 로고
    • For reviews of recent advancements in transition metal catalysis, see: a
    • For reviews of recent advancements in transition metal catalysis, see: a) D. M. D'Souza, T J. J. Müller, Chem. Soc. Rev. 2007, 36, 1095-1108;
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1095-1108
    • D'Souza, D.M.1    Müller, T.J.J.2
  • 17
    • 33947727055 scopus 로고    scopus 로고
    • For a review of Sonogashira coupling, see
    • For a review of Sonogashira coupling, see: R. Chinchilla, C. Nájera, Chem. Rev. 2007, 107, 874-922.
    • (2007) Chem. Rev. , vol.107 , pp. 874-922
    • Chinchilla, R.1    Nájera, C.2
  • 25
    • 0037170944 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: a) E. R. Jarvo, S. J. Miller, Tetrahedron 2002, 58, 2481-2495;
    • (2002) Tetrahedron , vol.58 , pp. 2481-2495
    • Jarvo, E.R.1    Miller, S.J.2
  • 28
    • 4143095871 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: a) B. List, Acc. Chem. Res. 2004, 37, 548-557;
    • (2004) Acc. Chem. Res. , vol.37 , pp. 548-557
    • List, B.1
  • 30
    • 33745715054 scopus 로고    scopus 로고
    • For a review on asymmetric iminium ion catalysis, see: a
    • For a review on asymmetric iminium ion catalysis, see: a) G. Leiais, D. W. C. MacMillan, Aldrichimica Acta 2006, 39, 79-87.
    • (2006) Aldrichimica Acta , vol.39 , pp. 79-87
    • Leiais, G.1    MacMillan, D.W.C.2
  • 31
    • 34250613134 scopus 로고    scopus 로고
    • For general organocatalytic asymmetric conjugate additions, see: b
    • For general organocatalytic asymmetric conjugate additions, see: b) S. B. Tsogoeva, Eur. J. Org. Chem. 2007, 1701-1716.
    • (2007) Eur. J. Org. Chem. , pp. 1701-1716
    • Tsogoeva, S.B.1
  • 36
    • 0034596299 scopus 로고    scopus 로고
    • For selected examples, see: a
    • For selected examples, see: a) W. Notz, B. List, J. Am. Chem. Soc, 2000, 122, 7386-7387;
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 7386-7387
    • Notz, W.1    List, B.2
  • 45
    • 0002782655 scopus 로고
    • Eds.: B. M. Trost, I. Fleming, Pergamon, Oxford
    • a) D. Caine, in: Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, Vol.3, pp. 1-63;
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 1-63
    • Caine, D.1
  • 47
    • 0003913629 scopus 로고    scopus 로고
    • Ed.: J. Otera, Wiley-VCH, Weinheim
    • c) Modem Carbonyl Chemistry (Ed.: J. Otera), Wiley-VCH, Weinheim, 2000.
    • (2000) Modem Carbonyl Chemistry
  • 48
    • 0000096952 scopus 로고
    • For Cannizzaro and Tishchenko side reactions, see: a
    • For Cannizzaro and Tishchenko side reactions, see: a) H. O. House, W. C. Liang, P. D. Weeks, J. Org. Chem. 1974, 39, 3102-3107;
    • (1974) J. Org. Chem. , vol.39 , pp. 3102-3107
    • House, H.O.1    Liang, W.C.2    Weeks, P.D.3
  • 55
    • 65549099061 scopus 로고    scopus 로고
    • An interesting alternative pathway to achieve stereoselectivity by linking the chiral enamine catalyst with phosphanes as both organocatalysts and ligands has been reported, although only low enantioselectivity was observed
    • An interesting alternative pathway to achieve stereoselectivity by linking the chiral enamine catalyst with phosphanes as both organocatalysts and ligands has been reported, although only low enantioselectivity was observed: T. Sato, K. Tomioka, HeIerocycles 2009, 77, 587-593.
    • (2009) HeIerocycles , vol.77 , pp. 587-593
    • Sato, T.1    Tomioka, K.2
  • 56
    • 34347229695 scopus 로고    scopus 로고
    • For a recent example of iridium-catalysed asymmetric allylation, see: D. J. Weix, J. F. Hartwig, J. Am. Chem. Soc. 2007, 129, 7720-7721.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 7720-7721
    • Weix, D.J.1    Hartwig, J.F.2
  • 59
    • 51049119177 scopus 로고    scopus 로고
    • For recent reviews of Cu catalysis, see: a
    • For recent reviews of Cu catalysis, see: a) S. Díez- González, S. P. Nolan, Aldrichimica Acta 2008, 41, 43-51.
    • (2008) Aldrichimica Acta , vol.41 , pp. 43-51
    • Díez-González, S.1    Nolan, S.P.2
  • 62
    • 34250824768 scopus 로고    scopus 로고
    • For recent reviews of Au catalysis, see: d
    • For recent reviews of Au catalysis, see: d) A. Fürstner, RW. Davies, Angew. Chem. Int. Ed, 2007, 46, 3410-3449;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 3410-3449
    • Fürstner, A.1    Davies, R.W.2
  • 63
  • 71
    • 0037043180 scopus 로고    scopus 로고
    • B. List, Tetrahedron 2002, 58, 5573-5590.
    • (2002) Tetrahedron , vol.58 , pp. 5573-5590
    • List, B.1
  • 79
    • 0004087670 scopus 로고
    • For the development of enamine chemistry, see: a Ed.: Z. Rappoport, Wiley, New York, For enamine catalysis, see ref. 11
    • For the development of enamine chemistry, see: a) The Chemistry of Enamines (Ed.: Z. Rappoport), Wiley, New York, 1994. For enamine catalysis, see ref. 11.
    • (1994) The Chemistry of Enamines
  • 88
    • 77952599148 scopus 로고    scopus 로고
    • The redox potential of phenacyl bromide is lower than that of the enamine intermediate; see ref 41
    • The redox potential of phenacyl bromide is lower than that of the enamine intermediate; see ref 41.
  • 91
    • 0003868337 scopus 로고    scopus 로고
    • Eds: P. W. N. M. van Leeuwen, C. Claver, Kluwer, Dordrecht
    • a) Rhodium-Catalyzed Hydroformylation (Eds: P. W. N. M. van Leeuwen, C. Claver), Kluwer, Dordrecht, 2000.
    • (2000) Rhodium-Catalyzed Hydroformylation
  • 110
    • 1542475798 scopus 로고    scopus 로고
    • For related studies, see also: a
    • For related studies, see also: a) J. Lacour, V. Hebbe-Viton, Chem. Soc. Rev. 2003, 32, 373-382;
    • (2003) Chem. Soc. Rev. , vol.32 , pp. 373-382
    • Lacour, J.1    Hebbe-Viton, V.2
  • 114
    • 0001708390 scopus 로고
    • For selected examples, see: e
    • For selected examples, see: e) H. Alper, N. Hamel, J. Am. Chem. Soc. 1990, 112, 2803-2804.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 2803-2804
    • Alper, H.1    Hamel, N.2
  • 118
  • 123
    • 53849148639 scopus 로고    scopus 로고
    • For a recent review, see: a) R. A. Widenhoefer, Chem. Eur. J. 2008, 14, 5382-5391.
    • (2008) Chem. Eur. J. , vol.14 , pp. 5382-5391
    • Widenhoefer, R.A.1
  • 134
    • 0000904753 scopus 로고    scopus 로고
    • For reviews of Mn-catalysed alkene epoxidation, see: a) T. Katsuki, Adv. Synth. Catal. 2002, 344, 131-147;
    • (2002) Adv. Synth. Catal. , vol.344 , pp. 131-147
    • Katsuki, T.1
  • 139
    • 33750167114 scopus 로고    scopus 로고
    • For a recent review on alkyne addition to imines, see: a) L. Zani, C. Bolm, Chem. Commun. 2006, 4263-4275.
    • (2006) Chem. Commun. , pp. 4263-4275
    • Zani, L.1    Bolm, C.2
  • 153
    • 33845579450 scopus 로고    scopus 로고
    • and ref 2o therein
    • For recent examples, see: X. Xie, Y. Chen, D. Ma, J. Am. Chem. Soc. 2006, 128, 16050-16051, and ref 2o therein.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 16050-16051
    • Xie, X.1    Chen, Y.2    Ma, D.3
  • 178
    • 38349148300 scopus 로고    scopus 로고
    • and also ref. 2 For representative examples, see
    • c) T. Hashimoto, K. Maruoka, Chem. Rev. 2007, 107, 5656-5682 and also ref. 2 For representative examples, see:
    • (2007) Chem. Rev. , vol.107 , pp. 5656-5682
    • Hashimoto, T.1    Maruoka, K.2
  • 208
    • 69949180302 scopus 로고    scopus 로고
    • For another example of a combination of alkene isomerization and aza-Petasis-Ferrier rearrangement, see: b) M. Terada, Y. Toda, J. Am. Chem. Soc. 2009, 757, 6354-6355.
    • (2009) J. Am. Chem. Soc. , vol.757 , pp. 6354-6355
    • Terada, M.1    Toda, Y.2
  • 219
    • 40549088216 scopus 로고    scopus 로고
    • For an recent account on metal-organic cooperative catalysis in C-H and C-C bond activation, see: Y. J. Park, J.-W. Park, C-H. Jun, Ace. Chem. Res. 2008, 41, 222-234.
    • (2008) Ace. Chem. Res. , vol.41 , pp. 222-234
    • Park, Y.J.1    Park, J.-W.2    Jun, C.-H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.