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Volumn 16, Issue 23, 1997, Pages 5027-5031

Formation of 1,3,5-trilithiobenzene and its conversion to the corresponding magnesium, mercury, and tin derivatives

Author keywords

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Indexed keywords


EID: 0000914709     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9705620     Document Type: Article
Times cited : (33)

References (28)
  • 11
    • 85033176377 scopus 로고
    • Brit. Patent 1,444,174
    • Massachusetts Institute of Technology, Brit. Patent 1,444,174; Chem. Abstr. 1977, 86, 106764t.
    • (1977) Chem. Abstr. , vol.86
  • 15
    • 0000956993 scopus 로고
    • and references cited herein
    • (b) Smith, B. J. Chem. Phys. Lett. 1993, 207, 403 and references cited herein.
    • (1993) Chem. Phys. Lett. , vol.207 , pp. 403
    • Smith, B.J.1
  • 18
    • 85033177969 scopus 로고    scopus 로고
    • Unpublished results
    • 1,3-Dilithiobenzene was synthesized in high yield by reaction of n-butyllithium and 1,3-dibromobenzene in refluxing hexane; Nijbacker, T. Unpublished results.
    • Nijbacker, T.1
  • 22
    • 85033168426 scopus 로고    scopus 로고
    • note
    • Preparation of 21 from 1,3-dibromobenzene and Mg in 2-MeTHF did not lead to precipitation of this product.
  • 26
    • 85033181485 scopus 로고    scopus 로고
    • note
    • The mass spectrum was identical with that of an authentic sample obtained via a different synthetic approach (from the reaction of 3 with trimethylstannyl sodium, paper to be published).
  • 27
    • 85033176727 scopus 로고    scopus 로고
    • note
    • The mass spectrum was identical with that of an authentic sample obtained from 2 and trimethylstannyl chloride.


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