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Volumn 14, Issue 10, 1995, Pages 4457-4459

New and Convenient Synthesis of Lithiated Allenes and Ketenimines Based on Readily Available Aryl-Substituted Ketones and Amides

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EID: 0003173310     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om00010a006     Document Type: Article
Times cited : (17)

References (18)
  • 7
    • 0006044979 scopus 로고
    • Formation of polylithioallenes is a facile process
    • Formation of polylithioallenes is a facile process: (a) Jaffe, F. J. Organomet. Chem. 1970, 23, 53.
    • (1970) Organomet. Chem. , vol.23 , pp. 53
    • Jaffe, F.J.1
  • 11
    • 33748495628 scopus 로고
    • 2 had been formed by the rearrangement of 1,2-dilithio-3,3-diphenylcyclopropene, the latter having been generated by the dilithiation of 3,3-diphenylcyclopropene by butyllithium
    • 2 had been formed by the rearrangement of 1,2-dilithio-3,3-diphenylcyclopropene, the latter having been generated by the dilithiation of 3,3-diphenylcyclopropene by butyllithium: Binger, P.; Müller, P.; Wenz, R.; Mynott, R. Angew. Chem., Int. Ed. Engl. 1990, 29, 1037.
    • (1990) Angew. Chem., Int. Ed. Engl. , vol.29 , pp. 1037
    • Binger, P.1    Müller, P.2    Wenz, R.3    Mynott, R.4
  • 12
    • 0006110481 scopus 로고
    • The spectroscopic properties and melting point (194–196 °C) were identical with those of cis-1,2-diphenyl-anti-3,4-dibenzylidenecyclobutane (mp 197 °C), which was prepared by heating 1,3-diphenylallene in refluxing benzene
    • The spectroscopic properties and melting point (194–196 °C) were identical with those of cis-1,2-diphenyl-anti-3,4-dibenzylidenecyclobutane (mp 197 °C), which was prepared by heating 1,3-diphenylallene in refluxing benzene: Dehmlow, E. V. Chem. Ber. 1967, 100, 3260.
    • (1967) Chem. Ber. , vol.100 , pp. 3260
    • Dehmlow, E.V.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.