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Volumn 21, Issue 11, 2002, Pages 2283-2292

Chelate ring size controls the formation of mixed complexes involving butyllithium and sodium amides

Author keywords

[No Author keywords available]

Indexed keywords

CHELATION; COMPLEXATION; DIMERS; LITHIUM COMPOUNDS; SODIUM COMPOUNDS;

EID: 0013326085     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om0109410     Document Type: Article
Times cited : (13)

References (68)
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    • Czech. Pat. 132.254; appl Dec 30, 1964
    • (i) Lochman, L.; Pospísil, J.; Lim, D. Czech. Pat. 132.254; appl Dec 30, 1964; Chem. Abstr. 1970, 73, 25642f.
    • Lochman, L.1    Pospísil, J.2    Lim, D.3
  • 49
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    • (i) Lochman, L.; Pospísil, J.; Lim, D. Czech. Pat. 132.254; appl Dec 30, 1964; Chem. Abstr. 1970, 73, 25642f.
    • (1970) Chem. Abstr. , vol.73
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    • Unimetal superbases
    • (j) Caubere, P. Unimetal Superbases. Chem. Rev. 1998, 1271.
    • (1998) Chem. Rev. , pp. 1271
    • Caubere, P.1
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    • Arvidsson, P. I.; Davidsson, Ö. Angew. Chem. 2000, 112, 1527-1530; Angew. Chem., Int. Ed. 2000, 39, 1467-1470.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 1467-1470
  • 56
    • 0038363196 scopus 로고    scopus 로고
    • note
    • This is no proof of dimeric species, but similar amides are known to form dimers in THF solutions.
  • 59
    • 0009562713 scopus 로고
    • n-Butyllithium was prepared according to published procedures; see: Hilmersson, G.; Davidsson, Ö. Organometallics 1995, 14(2), 912-918.
    • (1995) Organometallics , vol.14 , Issue.2 , pp. 912-918
    • Hilmersson, G.1    Davidsson, Ö.2
  • 62
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    • note
    • 2, pyrrolidine).
  • 63
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    • note
    • 2).
  • 64
    • 0038363195 scopus 로고    scopus 로고
    • note
    • 2, pyrrolidine).
  • 65
    • 0037687158 scopus 로고    scopus 로고
    • note
    • 2).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.