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Volumn , Issue 15, 2005, Pages 2625-2629

Preparation and reactions of highly functionalized bis-arylzinc reagents using a Li(acac)-catalyzed iodine-zinc exchange

Author keywords

Cross coupling; Functionalized zinc reagents; Halogen metal exchange; Nucleophilic catalysis

Indexed keywords

ALDEHYDES; CATALYSTS; IODINE; KETONES; LITHIUM; REACTION KINETICS;

EID: 26844550306     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-872097     Document Type: Article
Times cited : (23)

References (40)
  • 16
    • 29144530838 scopus 로고    scopus 로고
    • O'Neil, I., Ed.; Thieme: Stuttgart
    • (a) Knochel, P. Science of Synthesis, Vol. 3; O'Neil, I., Ed.; Thieme: Stuttgart, 2004, 5.
    • (2004) Science of Synthesis , vol.3 , pp. 5
    • Knochel, P.1
  • 20
    • 0039183328 scopus 로고
    • (b) Rieke, R. D. Science 1989, 246, 1260.
    • (1989) Science , vol.246 , pp. 1260
    • Rieke, R.D.1
  • 33
    • 0034936016 scopus 로고    scopus 로고
    • The alkynyl iodide 6 was obtained in two steps from commercially available 1-bromomethyl-2-iodobenzene in accordance to a literature procedure: Bouyssi, D.; Balme, G. Synlett 2001, 1191.
    • (2001) Synlett , pp. 1191
    • Bouyssi, D.1    Balme, G.2
  • 37
    • 26844439803 scopus 로고    scopus 로고
    • note
    • 2Zn) is decisive for the success of this procedure. Threefold titration and averaging have been typically done.
  • 38
    • 26844437054 scopus 로고    scopus 로고
    • note
    • The complete absence of LiCl is decisive for the success of the iodine-zinc exchange procedure.
  • 39
    • 26844527234 scopus 로고    scopus 로고
    • note
    • Threefold titration has been performed.
  • 40
    • 26844578582 scopus 로고    scopus 로고
    • note
    • 2O (1.3 equiv) in pyridine in the presence of DMAP (0.1 equiv).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.