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Volumn , Issue 11, 1998, Pages 1813-1824

Thermal decomposition of tert-butyl o-(phenoxy)- and o-(anilino)-phenyliminoxyperacetates

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EID: 33748632698     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a800868j     Document Type: Article
Times cited : (26)

References (113)
  • 3
    • 0001216647 scopus 로고
    • ed. B. M. Trost and I. Fleming, Pergamon Press, Oxford
    • D. P. Curran, Comprehensive Organic Synthesis, ed. B. M. Trost and I. Fleming, Pergamon Press, Oxford, 1991, vol. 4, p. 715;
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 715
    • Curran, D.P.1
  • 63
    • 33845183598 scopus 로고
    • L. Graine and M. Raban, Chem. Rev., 1989, 89, 689. Even aliphatic sulfenimides are sometimes difficult to obtain: see ref. 8(o).
    • (1989) Chem. Rev. , vol.89 , pp. 689
    • Graine, L.1    Raban, M.2
  • 66
    • 33748585833 scopus 로고    scopus 로고
    • The yields of 9 were not affected by dilution; this is consistent with cage recombination of 8 and tert-butoxyl radicals [see ref. 5(b) and references cited therein]
    • The yields of 9 were not affected by dilution; this is consistent with cage recombination of 8 and tert-butoxyl radicals [see ref. 5(b) and references cited therein].
  • 67
    • 33748628129 scopus 로고    scopus 로고
    • On the other hand, due to the complete absence of the corresponding acids in the starting peresters 6b,c, we can exclude that imines 12b,c might arise from those acids through a concerted mechanism similar to the one observed in the mass spectrometer
    • On the other hand, due to the complete absence of the corresponding acids in the starting peresters 6b,c, we can exclude that imines 12b,c might arise from those acids through a concerted mechanism similar to the one observed in the mass spectrometer.
  • 78
    • 0000777413 scopus 로고
    • It is worth noting that when the oxime 41 was treated with lead tetraacetate in boiling benzene - a well-known source of iminoxyl radicals (G. Just and K. Dahl, Tetrahedron, 1968, 24, 5251;
    • (1968) Tetrahedron , vol.24 , pp. 5251
    • Just, G.1    Dahl, K.2
  • 80
    • 33845471158 scopus 로고
    • - the reaction furnished small amounts of acridines 15 and 201, together with major amounts of ketone 31 (see: R. N. Butler, Chem. Rev., 1984, 84, 249)
    • (1984) Chem. Rev. , vol.84 , pp. 249
    • Butler, R.N.1
  • 81
    • 84970586185 scopus 로고
    • and other unidentified products. This result suggests that iminoxyl radicals 24 might be intermediates in the formation of the acridine derivatives. As far as the intermediacy of a carbenic species is concerned, it should be noted that acridine compounds have been obtained by intramolecular insertion of o-(arylamino)-phenylcarbenes in the gas phase (W. D. Crow and H. McNab, Aust. J. Chem., 1981, 34, 1037). The possibility that the acridines could also arise from cyclisation of other electrophilic species obtained by further oxidation of 24 should however be taken into account.
    • (1981) Aust. J. Chem. , vol.34 , pp. 1037
    • Crow, W.D.1    McNab, H.2
  • 87
    • 33748618847 scopus 로고
    • [Chem. Abstr., 1958, 52, 9006h].
    • (1958) Chem. Abstr. , vol.52
  • 89
    • 33748607351 scopus 로고
    • [Chem. Abstr., 1955, 49, 5373h].
    • (1955) Chem. Abstr. , vol.49
  • 102
    • 84917846702 scopus 로고
    • [Chem. Abstr., 1958, 52, 3719b].
    • (1958) Chem. Abstr. , vol.52
  • 104
    • 33748626427 scopus 로고    scopus 로고
    • Commercially available compound (Aldrich)
    • Commercially available compound (Aldrich).
  • 113
    • 33646767009 scopus 로고    scopus 로고
    • The ORTEP representation in Fig. 1 was obtained with ORTEP-3 for Windows. See: L. J. Farrugia, J. Appl. Crystallogr., 1997, 30, 565.
    • (1997) J. Appl. Crystallogr. , vol.30 , pp. 565
    • Farrugia, L.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.