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Volumn , Issue 11, 2005, Pages 1783-1786

Zr-catalyzed coupling reaction of alkyl halides, tosylates, and sulfates with β-phenethyl Grignard reagents via styrene-zirconate intermediates

Author keywords

phenethyl grignard reagent; Alkyl halide; Alkyl tosylate; Coupling reaction; Zirconocene

Indexed keywords

BETA PHENETHYLMAGNESIUM CHLORIDE; HALIDE; PHENETHYL ALCOHOL; STYRENE; SULFATE; TOLUENESULFONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; ZIRCONIUM;

EID: 22244433532     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-871572     Document Type: Article
Times cited : (18)

References (19)
  • 1
    • 0000220284 scopus 로고
    • Joyce, R. M., Ed.; John Wiley and Sons, Inc.: New York
    • Lipshutz, B. H.; Sengupta, S. In Organic Reactions, Vol. 41; Joyce, R. M., Ed.; John Wiley and Sons, Inc.: New York, 1992, 135.
    • (1992) Organic Reactions , vol.41 , pp. 135
    • Lipshutz, B.H.1    Sengupta, S.2
  • 11
    • 0003085584 scopus 로고
    • It is known that Ni-catalyzed cross-coupling reaction of aryl halides with isopropyl Grignand reagent affords n-propyl-benzene as the major product via isomerization of isopropyl group, see: Kiso, Y.; Tamao, K.; Kumada, K. J. Organomet. Chem. 1973, 50, C12.
    • (1973) Organomet. Chem. , vol.50
    • Kiso, Y.1    Tamao, K.2    Kumada, K.J.3
  • 16
    • 0032545046 scopus 로고    scopus 로고
    • s-Butylbenzene was formed in 81% yield by the direct reaction of EtOTs with PhCHMeMgBr in THF for 5 min at 50 °C. This result indicates that α-substituted benzyl Grignard reagents readily react with alkyl electrophiles, see also: Terao, J.; Saito, K.; Nu, S.; Kambe, N.; Sonoda, N. J. Am. Chem. Soc. 1998, 120, 11822.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 11822
    • Terao, J.1    Saito, K.2    Nu, S.3    Kambe, N.4    Sonoda, N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.