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Volumn 10, Issue 20, 2008, Pages 4633-4636

Silver-promoted domino Pd-catalyzed amination/direct arylation: Access to polycyclic heteroaromatics

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE DERIVATIVE; PALLADIUM; POLYCYCLIC HYDROCARBON; SILVER;

EID: 58149154405     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801932z     Document Type: Article
Times cited : (93)

References (38)
  • 1
    • 33846918696 scopus 로고    scopus 로고
    • For recent reviews on direct arylation, see: a
    • For recent reviews on direct arylation, see: (a) Alberico, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007, 107, 174.
    • (2007) Chem. Rev , vol.107 , pp. 174
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 5
    • 84891004791 scopus 로고    scopus 로고
    • Dyker, G, Ed, Wiley-VCH: Weinheim, Vols and 2
    • (e) Handbook of C - H Transformations; Dyker, G., Ed.; Wiley-VCH: Weinheim, 2005; Vols 1 and 2.
    • (2005) Handbook of C - H Transformations , vol.1
  • 9
    • 34250655628 scopus 로고    scopus 로고
    • and references cited therein
    • (i) Seregin, I. V.; Gevorgyan, V. Chem. Soc. Rev. 2007, 36, 1173, and references cited therein.
    • (2007) Chem. Soc. Rev , vol.36 , pp. 1173
    • Seregin, I.V.1    Gevorgyan, V.2
  • 10
    • 0347928722 scopus 로고    scopus 로고
    • For selected examples of tandem/domino processes involving direct arylation, see: a
    • For selected examples of tandem/domino processes involving direct arylation, see: (a) Wegner, H. A.; Scott, L. T.; de Meijere, A. J. Org. Chem. 2003, 68, 883.
    • (2003) J. Org. Chem , vol.68 , pp. 883
    • Wegner, H.A.1    Scott, L.T.2    de Meijere, A.3
  • 30
  • 31
    • 33846219497 scopus 로고    scopus 로고
    • For a review on acene- and heteroacene-based OED's, see
    • For a review on acene- and heteroacene-based OED's, see: Anthony, J. E. Chem. Rev. 2006, 106, 5028.
    • (2006) Chem. Rev , vol.106 , pp. 5028
    • Anthony, J.E.1
  • 32
    • 0037016413 scopus 로고    scopus 로고
    • For a review of halide effects in transition metal chemistry, see
    • For a review of halide effects in transition metal chemistry, see: Fagnou, K.; Lautens, M. Angew. Chem, Int. Ed. 2002, 41, 26.
    • (2002) Angew. Chem, Int. Ed , vol.41 , pp. 26
    • Fagnou, K.1    Lautens, M.2
  • 33
    • 31544455027 scopus 로고    scopus 로고
    • For the use of silver salts to sequester iodide in direct arylation reactions, see: a
    • For the use of silver salts to sequester iodide in direct arylation reactions, see: (a) Campeau, L.-C.; Parisien, M.; Jean, A.; Fagnou, K. J. Am. Chem. Soc. 2006, 128, 581.
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 581
    • Campeau, L.-C.1    Parisien, M.2    Jean, A.3    Fagnou, K.4
  • 35
    • 33748515918 scopus 로고    scopus 로고
    • 3 as a base in Rh-catalyzed direct arylation has also been described. See: Yanagisawa, S.; Sudo, T.; Noyori, R.; Itami, K. J. Am. Chem. Soc. 2006, 128, 11748.
    • 3 as a base in Rh-catalyzed direct arylation has also been described. See: Yanagisawa, S.; Sudo, T.; Noyori, R.; Itami, K. J. Am. Chem. Soc. 2006, 128, 11748.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.