메뉴 건너뛰기




Volumn , Issue , 2012, Pages 97-163

Selected Applications of Pd- and Cu-Catalyzed Carbon-Heteroatom Cross-Coupling Reactions in the Pharmaceutical Industry

Author keywords

Cu catalyzed C N couplings; Cu mediated oxidative boronic acid, heteroatom coupling; Pd and Cu catalyzed carbon heteroatom, selected applications; Pd or Cu catalyzed C P coupling; Pd or Cu catalyzed C S coupling

Indexed keywords


EID: 84886204040     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781118309872.ch3     Document Type: Chapter
Times cited : (15)

References (320)
  • 3
    • 52149114261 scopus 로고    scopus 로고
    • (c) Hartwig, J. F. Nature 2008, 455, 314-322.
    • (2008) Nature , vol.455 , pp. 314-322
    • Hartwig, J.F.1
  • 4
    • 34247568029 scopus 로고    scopus 로고
    • Buchwald-Hartwig amination
    • Li, J.J., Corey, E. J., Eds.; JohnWiley amp; Sons, Inc.: Hoboken, NJ
    • (d) Janey, J.M. Buchwald-Hartwig amination. In Name Reactions for Functional Group Transformations; Li, J. J., Corey, E. J., Eds.; JohnWiley amp; Sons, Inc.: Hoboken, NJ, 2007; pp. 564-609.
    • (2007) Name Reactions for Functional Group Transformations , pp. 564-609
    • Janey, J.M.1
  • 12
    • 84902433637 scopus 로고    scopus 로고
    • McCleverty, J. A.; Meyer, T. J., Eds.; Elsevier Ltd.: Oxford
    • (l) Hartwig, J. F. In Comprehensive Coordination Chemistry II; McCleverty, J. A.; Meyer, T. J., Eds.; Elsevier Ltd.: Oxford, 2004; Vol. 9, pp. 369-398.
    • (2004) Comprehensive Coordination Chemistry II , vol.9 , pp. 369-398
    • Hartwig, J.F.1
  • 18
    • 84874622103 scopus 로고    scopus 로고
    • Ackerman, L., Ed.; Wiley-VCH: Weinheim, Germany
    • (f) Thomas, A. W.; Ley, S. V. In Modern Arylation Methods; Ackerman, L., Ed.; Wiley-VCH: Weinheim, Germany, 2009; pp. 121-154.
    • (2009) Modern Arylation Methods , pp. 121-154
    • Thomas, A.W.1    Ley, S.V.2
  • 30
    • 0032510005 scopus 로고    scopus 로고
    • First used by Nishiyama for amination: Nishiyama, M.; Yamamoto, T.; Koie, Y
    • (a) First used by Nishiyama for amination: Nishiyama, M.; Yamamoto, T.; Koie, Y. Tetrahedron Lett. 1998, 39, 617.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 617
  • 33
    • 0001029926 scopus 로고
    • First developed by van Leeuwen: Kranenburg, M.; van der Burgt, Y.E.M.; Kamer, P. C. J.; van Leeuwen, P. W. N. M
    • (a) First developed by van Leeuwen: Kranenburg, M.; van der Burgt, Y. E. M.; Kamer, P. C. J.; van Leeuwen, P. W. N. M. Organometallics 1995, 14, 3081.
    • (1995) Organometallics , vol.14 , pp. 3081
  • 41
    • 84886103979 scopus 로고    scopus 로고
    • Novartis 2009 Annual Report: Healthcare Portfolio. Available at
    • Novartis 2009 Annual Report: Healthcare Portfolio. Available at http://www.novartis.com/downloads/investors/sales-results/Q4-2009-media-release_EN.pdf
  • 49
    • 84886177266 scopus 로고    scopus 로고
    • For beneficial effects of tert-amyl alcohol in palladium-catalyzed processes, see:
    • For beneficial effects of tert-amyl alcohol in palladium-catalyzed processes, see:
  • 121
    • 0345329013 scopus 로고
    • for an early review, see: Lindley, J. Tetrahedron
    • for an early review, see: Lindley, J. Tetrahedron 1984, 40, 1433-1456.
    • (1984) , vol.40 , pp. 1433-1456
  • 244
    • 84886178420 scopus 로고    scopus 로고
    • for a review, see: Chan, D.M.T.; Lam, P.Y.S. In Boronic Acids; Hall, D. G., Ed.; Wiley-VCH: Weinheim, See also Ref. 2e
    • for a review, see: Chan, D. M. T.; Lam, P. Y. S. In Boronic Acids; Hall, D. G., Ed.; Wiley-VCH: Weinheim, 2005; pp. 205-240. See also Ref. 2e.
    • (2005) , pp. 205-240
  • 257
    • 1542637623 scopus 로고    scopus 로고
    • For a review on transition metal-catalyzed carbon-boron bond formation, see: Ishiyama, T.; Miyaura, N
    • For a review on transition metal-catalyzed carbon-boron bond formation, see: Ishiyama, T.; Miyaura, N. Chem. Rec. 2004, 3, 271-280.
    • (2004) Chem. Rec. , vol.3 , pp. 271-280
  • 294
    • 0141522864 scopus 로고    scopus 로고
    • for reviews, see: Beletskaya, I.P.; Kazankova, M.A
    • (a) For reviews, see: Beletskaya, I. P.; Kazankova, M. A. Russ. J. Org. Chem. 2002, 38, 1391-1430.
    • (2002) Russ. J. Org. Chem. , vol.38 , pp. 1391-1430
  • 296
    • 67649283548 scopus 로고    scopus 로고
    • For a review on phosphonylation of heterocycles, see: Van der Jeught, S.; Stevens, C.V
    • (c) For a review on phosphonylation of heterocycles, see: Van der Jeught, S.; Stevens, C. V. Chem. Rev. 2009, 109, 2672-2702.
    • (2009) Chem. Rev. , vol.109 , pp. 2672-2702
  • 308
    • 77950505239 scopus 로고    scopus 로고
    • for Ni-catalyzed amination of aryl pivalates, see: Shimasaki, T.; Tobisu, M.; Chatani, N.Angew. Chem Also see references cited therein for other examples of Ni-catalyzed amination of aryl halides
    • For Ni-catalyzed amination of aryl pivalates, see: Shimasaki, T.; Tobisu, M.; Chatani, N. Angew. Chem., Int. Ed. 2010, 49, 2929. Also see references cited therein for other examples of Ni-catalyzed amination of aryl halides.
    • (2010) Int. Ed. , vol.49 , pp. 2929
  • 310
    • 76149123908 scopus 로고    scopus 로고
    • For a review, see: Serdyuk, O.V.; Abaev, V.T.
    • For a review, see: Serdyuk, O. V.; Abaev, V. T. Russ. Chem. Rev. 2009, 78, 1031-1045.
    • (2009) Russ. Chem. Rev. , vol.78 , pp. 1031-1045
  • 320
    • 84886224992 scopus 로고    scopus 로고
    • For a highlight, see: Armstrong, A.; Collins, J.C.Angew. Chem
    • For a highlight, see: Armstrong, A.; Collins, J. C. Angew. Chem., Int. Ed. 2010, 49, 2.
    • (2010) Int. Ed. , vol.49 , pp. 2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.