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Volumn 51, Issue 18, 2010, Pages 2427-2430

Generation of allyl Grignard reagents via titanocene-catalyzed activation of allyl halides

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL COMPOUND; CARBONYL DERIVATIVE; GRIGNARD REAGENT; HALIDE; NUCLEOPHILE; ORGANOMETALLIC COMPOUND; TITANOCENE;

EID: 77950022428     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.02.144     Document Type: Article
Times cited : (23)

References (49)
  • 7
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    • Silverman G.S., and Rakita P.E. (Eds), Marcell Dekker, New York
    • In: Silverman G.S., and Rakita P.E. (Eds). Handbook of Grignard Reagents (1996), Marcell Dekker, New York
    • (1996) Handbook of Grignard Reagents
  • 8
    • 4243893500 scopus 로고
    • For recent reviews on allylations, see:
    • For recent reviews on allylations, see:. Yamamoto Y., and Asao N. Chem. Rev. 93 (1993) 2207
    • (1993) Chem. Rev. , vol.93 , pp. 2207
    • Yamamoto, Y.1    Asao, N.2
  • 12
    • 0142245730 scopus 로고    scopus 로고
    • For reviews on allyl metal carbonyl additions, see:
    • For reviews on allyl metal carbonyl additions, see:. Kennedy J.W.J., and Hall D.G. Angew. Chem., Int. Ed. 42 (2003) 4732
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4732
    • Kennedy, J.W.J.1    Hall, D.G.2
  • 40
    • 0030599234 scopus 로고    scopus 로고
    • For the transition metal-catalyzed generation of Grignard reagents, see:
    • For the transition metal-catalyzed generation of Grignard reagents, see:. Takai K., Ueda T., Hayashi T., and Moriwake T. Tetrahedron Lett. 37 (1996) 7049
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7049
    • Takai, K.1    Ueda, T.2    Hayashi, T.3    Moriwake, T.4
  • 42
    • 77950021830 scopus 로고    scopus 로고
    • note
    • Other phosphines that restore catalytic activity at -40 °C: triphenylphosphine (95%), 1,2-bis(diphenylphosphino)ethane (94%), rac-BINAP (82%), tris(o-tolyl)phosphine (99%), tributylphosphine (95%).
  • 43
    • 0030458468 scopus 로고    scopus 로고
    • Allylation of ketones can be problematic, see:
    • Allylation of ketones can be problematic, see:. Fürstner A., and Shi N. J. Am. Chem. Soc. 118 (1996) 12349
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12349
    • Fürstner, A.1    Shi, N.2
  • 49
    • 0027244717 scopus 로고
    • The addition of an allyltitanium complex has been shown to proceed with in a diastereomeric ration of 2:1:
    • The addition of an allyltitanium complex has been shown to proceed with in a diastereomeric ration of 2:1:. Ireland R.E., Armstrong J.D., Lebreton J., Meissner R.S., and Rizzacasa M.A. J. Am. Chem. Soc. 115 (1993) 7152
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 7152
    • Ireland, R.E.1    Armstrong, J.D.2    Lebreton, J.3    Meissner, R.S.4    Rizzacasa, M.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.