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Volumn 13, Issue 12, 2011, Pages 3082-3085

C-H bond arylations and benzylations on oxazol(in)es with a palladium catalyst of a secondary phosphine oxide

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EID: 79958797661     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200986x     Document Type: Article
Times cited : (81)

References (76)
  • 5
  • 17
    • 79958790624 scopus 로고    scopus 로고
    • Select recent reviews on metal-catalyzed C-H bond functionalizations
    • Select recent reviews on metal-catalyzed C-H bond functionalizations: Hartwig, J. F. Chem. Soc. Rev. 2011, 40, 1992-2002
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 1992-2002
    • Hartwig, J.F.1
  • 42
    • 62349113696 scopus 로고    scopus 로고
    • For (heteroatom-substituted) secondary phosphine oxides in C-H bond functionalizations on indoles, see
    • For (heteroatom-substituted) secondary phosphine oxides in C-H bond functionalizations on indoles, see: Ackermann, L.; Barfüsser, S. Synlett 2009, 808-812
    • (2009) Synlett , pp. 808-812
    • Ackermann, L.1    Barfüsser, S.2
  • 43
    • 33847256803 scopus 로고    scopus 로고
    • For the use of a palladium catalyst derived from a secondary phosphine chloride in combination with Cu(Xantphos)I, see:; J. Am. Chem. Soc. 2010, 132, 3674-3675
    • Zhang, Z.; Hu, Z.; Yu, Z.; Lei, P.; Chi, H.; Wang, Y.; He, R. Tetrahedron Lett. 2007, 48, 2415-2419 For the use of a palladium catalyst derived from a secondary phosphine chloride in combination with Cu(Xantphos)I, see: Huang, J.; Chan, J.; Chen, Y.; Borths, C. J.; Baucom, K. D.; Larsen, R. D.; Faul, M. M. J. Am. Chem. Soc. 2010, 132, 3674-3675
    • (2007) Tetrahedron Lett. , vol.48 , pp. 2415-2419
    • Zhang, Z.1    Hu, Z.2    Yu, Z.3    Lei, P.4    Chi, H.5    Wang, Y.6    He, R.7    Huang, J.8    Chan, J.9    Chen, Y.10    Borths, C.J.11    Baucom, K.D.12    Larsen, R.D.13    Faul, M.M.14
  • 44
    • 50249139511 scopus 로고    scopus 로고
    • 2P(O)H as preligand in ruthenium-catalyzed C-H bond functionalizations, see
    • 2P(O)H as preligand in ruthenium-catalyzed C-H bond functionalizations, see: Ackermann, L.; Vicente, R.; Althammer, A. Org. Lett. 2008, 10, 2299-2302
    • (2008) Org. Lett. , vol.10 , pp. 2299-2302
    • Ackermann, L.1    Vicente, R.2    Althammer, A.3
  • 46
    • 77951184228 scopus 로고    scopus 로고
    • For a very recent example of palladium-catalyzed direct alkynylation, see
    • For a very recent example of palladium-catalyzed direct alkynylation, see: Kim, S. H.; Chang, S. Org. Lett. 2010, 12, 1868-1871
    • (2010) Org. Lett. , vol.12 , pp. 1868-1871
    • Kim, S.H.1    Chang, S.2
  • 48
    • 70350648987 scopus 로고    scopus 로고
    • Direct benzylations under basic reaction conditions were only recently developed. [Ru]
    • Direct benzylations under basic reaction conditions were only recently developed. [Ru]: Ackermann, L.; Novák, P. Org. Lett. 2009, 11, 4966-4969
    • (2009) Org. Lett. , vol.11 , pp. 4966-4969
    • Ackermann, L.1    Novák, P.2
  • 57
    • 79952050537 scopus 로고    scopus 로고
    • For recent progress in transition-metal-catalyzed direct arylations of heteroarenes, see
    • For recent progress in transition-metal-catalyzed direct arylations of heteroarenes, see: Kirchberg, S.; Tani, S.; Ueda, K.; Yamaguchi, J.; Studer, A.; Itami, K. Angew. Chem., Int. Ed. 2011, 50, 2387-2391
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 2387-2391
    • Kirchberg, S.1    Tani, S.2    Ueda, K.3    Yamaguchi, J.4    Studer, A.5    Itami, K.6
  • 73
    • 35348998959 scopus 로고    scopus 로고
    • references cited therein
    • Do, H.-Q.; Daugulis, O. J. Am. Chem. Soc. 2007, 129, 12404-12405 and references cited therein
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12404-12405
    • Do, H.-Q.1    Daugulis, O.2
  • 74
    • 0742321839 scopus 로고    scopus 로고
    • For an example of an elegant rhodium-catalyzed C-H bond functionalization, see
    • For an example of an elegant rhodium-catalyzed C-H bond functionalization, see: Lewis, J. C.; Wiedemann, S. H.; Bergman, R. G.; Ellman, J. A. Org. Lett. 2004, 6, 35-38
    • (2004) Org. Lett. , vol.6 , pp. 35-38
    • Lewis, J.C.1    Wiedemann, S.H.2    Bergman, R.G.3    Ellman, J.A.4
  • 76
    • 79958790623 scopus 로고    scopus 로고
    • This result is indicative of a reaction manifold involving an initial in situ deprotonation with the base LiO t -Bu
    • This result is indicative of a reaction manifold involving an initial in situ deprotonation with the base LiO t -Bu.


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