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Volumn 70, Issue 25, 2005, Pages 10420-10425

Palladium-catalyzed cross-coupling reactions of 2-iodo-4- (phenylchalcogenyl)-1-butenes

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; DERIVATIVES; PALLADIUM; REACTION KINETICS;

EID: 28744437354     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo051709x     Document Type: Article
Times cited : (15)

References (89)
  • 7
    • 0001487604 scopus 로고    scopus 로고
    • For the synthesis of MCPs, see: Brandi, A.; Goti, A. Chem. Rev. 1998, 98, 589.
    • (1998) Chem. Rev. , vol.98 , pp. 589
    • Brandi, A.1    Goti, A.2
  • 54
    • 33847802782 scopus 로고
    • The mechanism for the isomerization of the double bond in the Heck coupling reaction has been proposed already by Heck and co-workers (see Scheme 2). (a) Dieck, A.; Heck, R. F. J. Org. Chem. 1975, 40, 1083.
    • (1975) J. Org. Chem. , vol.40 , pp. 1083
    • Dieck, A.1    Heck, R.F.2
  • 60
    • 0033610452 scopus 로고    scopus 로고
    • and references therein
    • For some more recent related papers, please see: (b) Huang, J.; Nolan, S. P. J. Am. Chem. Soc. 1999, 121, 9889 and references therein.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9889
    • Huang, J.1    Nolan, S.P.2
  • 86
    • 28744440753 scopus 로고    scopus 로고
    • note
    • The optimization of the reaction conditions is summarized in the Supporting Information.
  • 87
    • 6044274630 scopus 로고    scopus 로고
    • The intramolecular chelation in the intermediate G obliges the hydride to be cis at the iodine and this is important for the reductive elimination, see: Hills, I. D.; Fu, G. C. J. Am. Chem. Soc. 2004, 126, 13178.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 13178
    • Hills, I.D.1    Fu, G.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.