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Volumn 29, Issue 8, 1990, Pages 927-929

A 1,6‐Diphospha‐1,2,4,5‐hexatetraene, Synthesis and Ring Closure Reactions to Cyclobutenes

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EID: 33748517668     PISSN: 05700833     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.199009271     Document Type: Article
Times cited : (47)

References (18)
  • 4
    • 0001451066 scopus 로고
    • Aus der Chemie der Carbenoide und anderer thermolabiler Organolithium-Verbindungen
    • See. e.g.
    • (1972) Angewandte Chemie , vol.84 , pp. 557
    • Köbrich, G.1
  • 6
    • 84990085404 scopus 로고    scopus 로고
    • −3. Further details of the crystal structure investigation are available on request from the Fachinformationszentrum Karlsruhe, Gesellschaft für wissenschaftlich‐technische Information mbH, D‐7514 Eggenstein‐Leopoldshafen 2 (FRG), on quoting the depository number CSD‐54659, the names of the authors, and the journal citation.
  • 7
    • 84990121130 scopus 로고    scopus 로고
    • max = 210 nm (Ig ε = 4.71), 250 (4.46), 296 (4.64), 305 (4.61), 367 (3.91).
  • 9
    • 84990093235 scopus 로고    scopus 로고
    • max = 218 nm (Igε = 4.69), 260 (4.54), 310 (sh, 4.01) [8].
  • 10
    • 84990121136 scopus 로고    scopus 로고
    • The phosphaallenes Aryl – P = C = CHR absorb at 220 nm, the molar extinctions ε = 20000–25000 are about half that of 4.
  • 11
    • 84990121114 scopus 로고    scopus 로고
    • −1 [9e].
  • 17
    • 84990093256 scopus 로고    scopus 로고
    • max = 230 nm (lg ε = 4.40), 289 (4.51), 306 (4.42), 360(sh, 3.97).
  • 18
    • 84990168889 scopus 로고    scopus 로고
    • Thus, the fact that all NMR signals appear only singly in 5, despite the unsymmetrical structure, cannot be explained in terms of a rapid ring‐opening 5 → 4 and renewed conrotatory ring closure. The mechanism required from the (Formula Presented.) NMR data, rapid degenerated rearrangement (a)–with exclusion of a synchronous inversion at the phosphorus atoms–is still unclear.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.