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Volumn 28, Issue 3, 2009, Pages 933-936

Organoheteroatom stannanes in palladium-catalyzed cross-coupling reactions with 1-naphthyl triflate

Author keywords

[No Author keywords available]

Indexed keywords

SUGAR (SUCROSE); SYNTHESIS (CHEMICAL);

EID: 61849184995     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om8009816     Document Type: Article
Times cited : (25)

References (56)
  • 1
    • 61849165125 scopus 로고    scopus 로고
    • Farina, V.; Krishnamurthy, V.; Scott, W. J. The Stille Reaction; Paquette, L. A., Ed.; Wiley: New York, 1997; Organic Reactions, 50.
    • Farina, V.; Krishnamurthy, V.; Scott, W. J. The Stille Reaction; Paquette, L. A., Ed.; Wiley: New York, 1997; Organic Reactions, Vol. 50.
  • 2
    • 0037442333 scopus 로고    scopus 로고
    • For some examples of C-N bond formation see: a
    • For some examples of C-N bond formation see: (a) Kim, Y. O.; Yu, S. J. Am. Chem. Soc. 2003, 125, 1696-1697.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 1696-1697
    • Kim, Y.O.1    Yu, S.2
  • 7
    • 33845281574 scopus 로고
    • For C-As and C-Sb see
    • (f) Tunney, S. E.; Stille, J. K. J. Org. Chem. 1987, 52, 748-753. For C-As and C-Sb see:
    • (1987) J. Org. Chem , vol.52 , pp. 748-753
    • Tunney, S.E.1    Stille, J.K.2
  • 52
    • 61849175383 scopus 로고    scopus 로고
    • Naphthalen-1-ylphenylselenide was isolated in yields ca. 10-15% lower than those found in CG yield. This yield was not optimized.
    • Naphthalen-1-ylphenylselenide was isolated in yields ca. 10-15% lower than those found in CG yield. This yield was not optimized.
  • 56
    • 61849134482 scopus 로고
    • Chem. Abstr. 1955, 49, 8843d.
    • (1955) Chem. Abstr , vol.49


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.