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Volumn 118, Issue 11, 1996, Pages 2758-2759

A new entry into cyclo[n]carbons: [2 + 2] cycloreversion of propellane-annelated dehydroannulenes

Author keywords

[No Author keywords available]

Indexed keywords

MACROCYCLIC COMPOUND; POLYCYCLIC HYDROCARBON;

EID: 0029872244     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja952801l     Document Type: Article
Times cited : (42)

References (30)
  • 1
    • 33748231383 scopus 로고
    • For reviews, see: (a) Diederich, F.; Rubin, Y. Angew. Chem., Int. Ed. Engl. 1992, 31, 1101. (b) Diederich, F. Nature 1994, 369, 199. (c) Diederich, F. In Modern Acetylene Chemistry; Stang, P. J., Diederich, F., Eds., VCH Publishers: Weinheim, Germany, 1995; p 443.
    • (1992) Angew. Chem., Int. Ed. Engl. , vol.31 , pp. 1101
    • Diederich, F.1    Rubin, Y.2
  • 2
    • 0028236962 scopus 로고
    • For reviews, see: (a) Diederich, F.; Rubin, Y. Angew. Chem., Int. Ed. Engl. 1992, 31, 1101. (b) Diederich, F. Nature 1994, 369, 199. (c) Diederich, F. In Modern Acetylene Chemistry; Stang, P. J., Diederich, F., Eds., VCH Publishers: Weinheim, Germany, 1995; p 443.
    • (1994) Nature , vol.369 , pp. 199
    • Diederich, F.1
  • 3
    • 0001350591 scopus 로고
    • Stang, P. J., Diederich, F., Eds., VCH Publishers: Weinheim, Germany
    • For reviews, see: (a) Diederich, F.; Rubin, Y. Angew. Chem., Int. Ed. Engl. 1992, 31, 1101. (b) Diederich, F. Nature 1994, 369, 199. (c) Diederich, F. In Modern Acetylene Chemistry; Stang, P. J., Diederich, F., Eds., VCH Publishers: Weinheim, Germany, 1995; p 443.
    • (1995) Modern Acetylene Chemistry , pp. 443
    • Diederich, F.1
  • 13
    • 2442651374 scopus 로고
    • Stang, P. J., Diederich, F., Eds.; VCH Publishers: Weinheim, Germany
    • (f) Plattner, D. A.; Li, Y.; Houk, K. N. In Modern Acetylene Chemistry. Stang, P. J., Diederich, F., Eds.; VCH Publishers: Weinheim, Germany, 1995; p 1
    • (1995) Modern Acetylene Chemistry , pp. 1
    • Plattner, D.A.1    Li, Y.2    Houk, K.N.3
  • 25
    • 85085782161 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra of 1 and 2 are also in accord with the diatropic and paratropic characters of the [18]-annulene and [24]annulene perimeters, respectively. Details are listed in the supporting information.
  • 27
    • 85085781626 scopus 로고    scopus 로고
    • note
    • 3i isomer of 6.
  • 28
    • 85085781426 scopus 로고    scopus 로고
    • note
    • 3) of 1. 4. 5. and 6 are observed at 356 (∈ 60 200), 367 (∈ 50 800), 376 (∈ 48 200), and 387 (∈ 57 000) nm, respectively. For details, see Figure 5 in the supporting information


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.