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Volumn 46, Issue 6, 2007, Pages 1924-1935

Reactions of hypervalent iodine reagents with palladium: Mechanisms and applications in organic synthesis

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EID: 34047101384     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic0620337     Document Type: Review
Times cited : (356)

References (167)
  • 6
    • 0842275310 scopus 로고    scopus 로고
    • Hypervalent Iodine Chemistry, Modern Developments in Organic Synthesis
    • Wirth, T, Ed, Springer: New York
    • (f) Wirth, T., Ed. Hypervalent Iodine Chemistry, Modern Developments in Organic Synthesis. Topics in Current Chemistry; Springer: New York, 2003; Vol. 224.
    • (2003) Topics in Current Chemistry , vol.224
  • 7
    • 2042507954 scopus 로고    scopus 로고
    • Suzuki-Miyaura reactions: (a) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457-2483.
    • Suzuki-Miyaura reactions: (a) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457-2483.
  • 10
    • 84985570392 scopus 로고    scopus 로고
    • Stille reactions: (d) Stille, J. K. Angew. Chem., Int. Ed. Engl. 1986, 25, 508-523.
    • Stille reactions: (d) Stille, J. K. Angew. Chem., Int. Ed. Engl. 1986, 25, 508-523.
  • 12
    • 0037943974 scopus 로고    scopus 로고
    • Sonogashira reactions: (f) Negishi, E.; Anastasia, L. Chem. Rev. 2003, 103, 1979-2017.
    • Sonogashira reactions: (f) Negishi, E.; Anastasia, L. Chem. Rev. 2003, 103, 1979-2017.
  • 13
    • 0034249671 scopus 로고    scopus 로고
    • Heck reactions: (g) Beletskaya, I. P.; Cheprakov, A. V. Chem. Rev. 2000, 100, 3009-3066.
    • Heck reactions: (g) Beletskaya, I. P.; Cheprakov, A. V. Chem. Rev. 2000, 100, 3009-3066.
  • 14
    • 34047140515 scopus 로고    scopus 로고
    • C-O and C-N reactions: (h) Muci, A. R.; Buchwald, S. L. Top. Curr. Chem. 2002, 219, 131-209.
    • C-O and C-N reactions: (h) Muci, A. R.; Buchwald, S. L. Top. Curr. Chem. 2002, 219, 131-209.
  • 19
    • 0000001683 scopus 로고    scopus 로고
    • C-heteroatom bond formation: (a) Stang, J. P.; Surber, B. W.; Chen, Z.-C.; Roberts, K. A.; Anderson, A. G. J. Am. Chem. Soc. 1987, 109, 228-235.
    • C-heteroatom bond formation: (a) Stang, J. P.; Surber, B. W.; Chen, Z.-C.; Roberts, K. A.; Anderson, A. G. J. Am. Chem. Soc. 1987, 109, 228-235.
  • 26
    • 34047137288 scopus 로고    scopus 로고
    • Carbonylation: (a) Uchiyama, M.; Suzuki, T.; Yamazaki, Y. Chem. Lett. 1983, 1201-1202.
    • Carbonylation: (a) Uchiyama, M.; Suzuki, T.; Yamazaki, Y. Chem. Lett. 1983, 1201-1202.
  • 47
    • 34047119302 scopus 로고    scopus 로고
    • Reductive coupling: (a) Uchiyama, M.; Suzuki, T.; Yamazaki, Y. Chem. Lett. 1983, 1165-1166.
    • Reductive coupling: (a) Uchiyama, M.; Suzuki, T.; Yamazaki, Y. Chem. Lett. 1983, 1165-1166.
  • 50
    • 0026637638 scopus 로고    scopus 로고
    • Stille coupling: (a) Moriarty, R. M.; Epa, W. R. Tetrahedron Lett. 1992, 33, 4095-4098.
    • Stille coupling: (a) Moriarty, R. M.; Epa, W. R. Tetrahedron Lett. 1992, 33, 4095-4098.
  • 60
    • 21844498149 scopus 로고    scopus 로고
    • Suzuki-Miyaura coupling: (a) Bumagin, N. A.; Luzikova, E. V.; Sukhomlinova, L. I.; Tolstaya, T. P.; Beletskaya, I. P. Russ. Chem. Bull. 1995, 44, 385-386.
    • Suzuki-Miyaura coupling: (a) Bumagin, N. A.; Luzikova, E. V.; Sukhomlinova, L. I.; Tolstaya, T. P.; Beletskaya, I. P. Russ. Chem. Bull. 1995, 44, 385-386.
  • 70
    • 85016541020 scopus 로고    scopus 로고
    • Heck reactions: (a) Sugioka, K.; Uchiyama, M.; Suzuki, T.; Yamazaki, Y. Nippon Kagaku Kaishi 1985, 527-532.
    • Heck reactions: (a) Sugioka, K.; Uchiyama, M.; Suzuki, T.; Yamazaki, Y. Nippon Kagaku Kaishi 1985, 527-532.
  • 83
    • 21844484301 scopus 로고    scopus 로고
    • Sonogashira coupling: (a) Luzikova, E. V.; Sukhomlinova, L. I.; Tolstaya, T. P.; Bumagin, N. A.; Beletskaya, I. P. Russ. Chem. Bull. 1995, 44, 556-557.
    • Sonogashira coupling: (a) Luzikova, E. V.; Sukhomlinova, L. I.; Tolstaya, T. P.; Bumagin, N. A.; Beletskaya, I. P. Russ. Chem. Bull. 1995, 44, 556-557.
  • 90
    • 0031950987 scopus 로고    scopus 로고
    • Transmetalation from other metals: (a) Huang, X.; Sun, A.-M. Synth. Commun. 1998, 28, 773-778.
    • Transmetalation from other metals: (a) Huang, X.; Sun, A.-M. Synth. Commun. 1998, 28, 773-778.
  • 97
    • 0032499085 scopus 로고    scopus 로고
    • Cyclization reactions: (a) Kang, S.-K.; Yamaguchi, T.; Pyun, S.-J.; Lee, Y.-T.; Baik, T.-G. Tetrahedron Lett. 1998, 39, 2127-2130.
    • Cyclization reactions: (a) Kang, S.-K.; Yamaguchi, T.; Pyun, S.-J.; Lee, Y.-T.; Baik, T.-G. Tetrahedron Lett. 1998, 39, 2127-2130.
  • 100
    • 0033961226 scopus 로고    scopus 로고
    • o-Hydroxyaldehyde arylation: (d) Xia, M.; Chen, Z.-C. Synth. Commun. 2000, 30, 531 -536.
    • o-Hydroxyaldehyde arylation: (d) Xia, M.; Chen, Z.-C. Synth. Commun. 2000, 30, 531 -536.
  • 102
    • 34047159365 scopus 로고    scopus 로고
    • Malonate arylation: (f) Oh, C. H.; Kim, J. S.; Jung, H. H. J. Org. Chem. 1999, 64, 1338-1340.
    • Malonate arylation: (f) Oh, C. H.; Kim, J. S.; Jung, H. H. J. Org. Chem. 1999, 64, 1338-1340.
  • 105
    • 37049129234 scopus 로고    scopus 로고
    • Analogous transmetalation reactions are well-known to occur in cross-coupling reactions with organomercury and organothallium reagents, a Uemura, S, Zushi, K, Okano, M, Ichikawa, K. J. Chem. Soc, Chem. Commun. 1972, 234-235
    • Analogous transmetalation reactions are well-known to occur in cross-coupling reactions with organomercury and organothallium reagents, (a) Uemura, S.; Zushi, K.; Okano, M.; Ichikawa, K. J. Chem. Soc., Chem. Commun. 1972, 234-235.
  • 107
    • 0000702671 scopus 로고
    • (c) Heck, R. F. Org. React. 1982, 27, 345-390.
    • (1982) Org. React , vol.27 , pp. 345-390
    • Heck, R.F.1
  • 112
    • 0346387650 scopus 로고    scopus 로고
    • Kurosawa, H, Yamamoto, A, Eds, Elsevier: New York
    • (c) In Fundamentals of Molecular Catalysis; Kurosawa, H., Yamamoto, A., Eds.; Elsevier: New York, 2003.
    • (2003) Fundamentals of Molecular Catalysis
  • 137
  • 142
    • 0012233552 scopus 로고    scopus 로고
    • For reviews that discuss catalytic-directed C-H activation/C-C bond formation, see: (a) Shilov, A. E.; Shul'pin, G. B. Chem. Rev. 1997, 97, 2879-2932.
    • For reviews that discuss catalytic-directed C-H activation/C-C bond formation, see: (a) Shilov, A. E.; Shul'pin, G. B. Chem. Rev. 1997, 97, 2879-2932.
  • 161
    • 20444370318 scopus 로고    scopus 로고
    • II/0-catalyzed arylation of indoles, see: (a) Lane, B. S.; Brown, M. A.; Sames, D. J. Am. Chem. Soc. 2005, 127, 8050-8057.
    • II/0-catalyzed arylation of indoles, see: (a) Lane, B. S.; Brown, M. A.; Sames, D. J. Am. Chem. Soc. 2005, 127, 8050-8057.
  • 167
    • 34047166548 scopus 로고    scopus 로고
    • manuscript in preparation
    • Desai, L. V.; Sanford, M. S., manuscript in preparation, 2006.
    • (2006)
    • Desai, L.V.1    Sanford, M.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.