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Volumn 69, Issue 19, 2004, Pages 6427-6432

Sequential reactions of trimethylstannyl anions with vinyl chlorides and dichlorides by the SRN1 mechanism followed by palladium-catalyzed cross-coupling processes

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIA; CATALYSIS; MIXTURES; NEGATIVE IONS; OLEFINS; REACTION KINETICS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 4644298003     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo049287z     Document Type: Article
Times cited : (15)

References (54)
  • 6
    • 0041474899 scopus 로고    scopus 로고
    • For a discussion of different mechanisms for vinylic substitutions, see: Galli, C.; Rappoport, Z. Acc. Chem. Res. 2003, 36, 580-587.
    • (2003) Acc. Chem. Res. , vol.36 , pp. 580-587
    • Galli, C.1    Rappoport, Z.2
  • 15
    • 0001300928 scopus 로고
    • RN1 reaction of organic halides
    • Patai S., Rappoport, Z., Eds.; Wiley: Chichester, U.K., Chapter 24
    • RN1 Reaction of Organic Halides. In The Chemistry of functional Groups; Patai S., Rappoport, Z., Eds.; Wiley: Chichester, U.K., 1995; Suppl. D2, Chapter 24, p 1395.
    • (1995) The Chemistry of Functional Groups , Issue.SUPPL. D2 , pp. 1395
    • Rossi, R.A.1    Pierini, A.B.2    Peñéñory, A.B.3
  • 16
    • 0001887447 scopus 로고    scopus 로고
    • RN1 reaction
    • Paquette, L. A., Bittman, R., Eds.; John Wiley & Sons, Inc.: New York
    • RN1 Reaction. In Organic Reactions; Paquette, L. A., Bittman, R., Eds.; John Wiley & Sons, Inc.: New York, 1999; Vol. 54, p 1.
    • (1999) Organic Reactions , vol.54 , pp. 1
    • Rossi, R.A.1    Pierini, A.B.2    Santiago, A.N.3
  • 18
    • 0000802361 scopus 로고    scopus 로고
    • The stille reaction
    • Paquette, L. A., Ed.; John Wiley & Sons, Inc.: New York
    • For reviews, see: (a) Farina, V.; Krishnamurthy, V.; Scott, W. J. The Stille Reaction. In Organic Reactions; Paquette, L. A., Ed.; John Wiley & Sons, Inc.: New York, 1997; Vol. 50, p 1.
    • (1997) Organic Reactions , vol.50 , pp. 1
    • Farina, V.1    Krishnamurthy, V.2    Scott, W.J.3
  • 19
    • 0000725544 scopus 로고    scopus 로고
    • Diederich, F., Stang, P. J., Eds.; Wiley-VCH Verlag GmbH: Weinheim, Germany
    • (b) Mitchell, T. N. In Metal Catalysed Cross-Coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH Verlag GmbH: Weinheim, Germany, 1998; p 167.
    • (1998) Metal Catalysed Cross-Coupling Reactions , pp. 167
    • Mitchell, T.N.1
  • 44
    • 4644326893 scopus 로고    scopus 로고
    • note
    • 4Sn. It is more difficult to transfer a methyl group than a vinyl moiety.
  • 52
    • 4644293009 scopus 로고    scopus 로고
    • note
    • M. Alami et al. obtained this compound by palladium-catalyzed cross-coupling reaction of 1-(2-iodo-2-phenylvinyl)naphthalene and phenylzinc chloride in 79% yield. The spectroscopic data agreed with those reported in the literature, ref 25.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.