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Volumn 45, Issue 3, 2006, Pages 465-468

Unsaturated fatty alcohol derivatives as a source of substituted allylzirconocene

Author keywords

Alcohols; Allylic compounds; C H activation; Elimination; Zirconium

Indexed keywords

ALCOHOLS; CARBON; ETHERS; REACTION KINETICS; ZIRCONIUM COMPOUNDS;

EID: 30444439065     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200501946     Document Type: Article
Times cited : (35)

References (52)
  • 1
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    • (Ed.: J. Otera), Wiley-VCH, Weinheim, chap. 10
    • For recent reviews of allylmetal addition, see a) S. R. Chemler, W. R. Roush in Modern Carbonyl Chemistry (Ed.: J. Otera), Wiley-VCH, Weinheim, 2000, chap. 10;
    • (2000) Modern Carbonyl Chemistry
    • Chemler, S.R.1    Roush, W.R.2
  • 4
    • 0002446724 scopus 로고
    • (Eds. B. M. Trost, I. Fleming, C. H. Heathcock), Pergamon, Oxford
    • d) W. R. Roush in Comprehensive Organic Synthesis, Vol. 2 (Eds. B. M. Trost, I. Fleming, C. H. Heathcock), Pergamon, Oxford, 1991, p. 1;
    • (1991) Comprehensive Organic Synthesis, Vol. 2 , vol.2 , pp. 1
    • Roush, W.R.1
  • 23
    • 23944522066 scopus 로고    scopus 로고
    • Carbometallation Reactions
    • (Eds.: A. de Meijere, F. Diederich), Wiley-VCH
    • b) "Carbometallation Reactions": I. Marek in Metal-Catalyzed Cross-Coupling Reactions, 2nd ed. (Eds.: A. de Meijere, F. Diederich), Wiley-VCH, 2004, p. 395;
    • (2004) Metal-Catalyzed Cross-Coupling Reactions, 2nd Ed. , pp. 395
    • Marek, I.1
  • 24
    • 11844260912 scopus 로고    scopus 로고
    • Synthesis and Reactivity of Allyltitanium Derivatives
    • (Ed.: I. Marek), Wiley-VCH, Weinheim
    • c) "Synthesis and Reactivity of Allyltitanium Derivatives": J. Szymoniak, C. Moise in Titanium and Zirconium in Organic Synthesis (Ed.: I. Marek), Wiley-VCH, Weinheim, 2002, p. 451.
    • (2002) Titanium and Zirconium in Organic Synthesis , pp. 451
    • Szymoniak, J.1    Moise, C.2
  • 29
    • 0003417469 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford
    • a) J. J. Eisch in Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford 1991, p. 8, 11;
    • (1991) Comprehensive Organic Synthesis , pp. 8
    • Eisch, J.J.1
  • 35
    • 0024029345 scopus 로고
    • b) S. Karlsson, A. Hallberg, S. Gronowitz, Chem. Scr. 1988, 27, 185. If an excess of the Schwartz reagent is used, the in situ formed terminal alkene undergoes a further hydrozirconation reaction to give the alkylzirconocene derivative.
    • (1988) Chem. Scr. , vol.27 , pp. 185
    • Karlsson, S.1    Hallberg, A.2    Gronowitz, S.3
  • 38
    • 0012477009 scopus 로고    scopus 로고
    • Synthesis and Reactivity of Zirconocene Derivatives
    • (Ed.: I. Marek), Wiley-VCH, Weinheim
    • c) "Synthesis and Reactivity of Zirconocene Derivatives": E. Negishi, S. Huo in Titanium and Zirconium in Organic Synthesis (Ed.: I. Marek), Wiley-VCH, Weinheim, 2002, p. 1.
    • (2002) Titanium and Zirconium in Organic Synthesis , pp. 1
    • Negishi, E.1    Huo, S.2
  • 42
    • 23944523083 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Dienyl Zirconocene Complexes
    • (Ed.: I. Marek), Springer, Berlin
    • c) "Stereoselective Synthesis of Dienyl Zirconocene Complexes": N. Chinkov, I. Marek in Topics on Organometallic Chemistry, Vol. 10 (Ed.: I. Marek), Springer, Berlin, 2004, p. 133;
    • (2004) Topics on Organometallic Chemistry, Vol. 10 , vol.10 , pp. 133
    • Chinkov, N.1    Marek, I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.