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Volumn 68, Issue 3, 2003, Pages 1067-1074

Phenonium ions from the addition of phenyl cations to alkenes. Photochemical synthesis of (rearranged) aminoalkylanilines from haloanilines in the presence of alkenes and amines

Author keywords

[No Author keywords available]

Indexed keywords

PHOTOELECTROLYSIS;

EID: 0037423165     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo026516d     Document Type: Article
Times cited : (36)

References (74)
  • 30
    • 0346194628 scopus 로고    scopus 로고
    • note
    • (a) Phenylium cations (ref 8b,c) have been obtained in solution only under particular conditions, allowing for little exploration of the chemistry, such as solvolysis of some perfluoroalkylsulfonic aryl esters (ref 8d-g), by solvolytic cyclization of (trifluoromethanesulfonyl)-oxydienynes (ref 8h-j), and by controlled (photo)decomposition af diazonium salts (ref 8k-q).
  • 31
    • 0000144392 scopus 로고    scopus 로고
    • Rappoport, Z., Stang, P. J., Eds.; Wiley: New York
    • (b) Stang, P. J. In Dicordinated Carbocations; Rappoport, Z., Stang, P. J., Eds.; Wiley: New York, 1997; p 451.
    • (1997) Dicordinated Carbocations , pp. 451
    • Stang, P.J.1
  • 51
    • 0002346717 scopus 로고    scopus 로고
    • Rappoport, Z., Stang, P. J., Eds.; Wiley: New York
    • (e) Speranza, M. In Dicordinated Carbocations; Rappoport, Z., Stang, P. J., Eds.; Wiley: New York, 1997; p 157.
    • (1997) Dicordinated Carbocations , pp. 157
    • Speranza, M.1
  • 64
    • 0346825244 scopus 로고    scopus 로고
    • note
    • Computation performed by Dr: M. Freccero in this Department; see Experimental Section.
  • 66
    • 84914643416 scopus 로고
    • See, e.g.: Sharpe, C. J.; Palmer, P. J.; Evans, D. E.; Brown, G. R.; King, G.; Shadholt, R. S.; Trigg, R. B.; Ward, R. J.; Ashford, A.; Ross, J. W. J. Med. Chem. 1972, 15, 523. Milligan, B.; Holt, L. A. J. Soc. Dyers Colour. 1978, 94, 352. Mathison, I. W.; Solomon, W. E. In Isoquinolines; Kathawala, F. G., Coppola, G. M., Schuster, H. F., Eds; Wiley: New York, 1990; Vol. 2, p 367.
    • (1978) Soc. Dyers Colour. , vol.94 , pp. 352
    • Milligan, B.1    Holt, L.A.J.2
  • 67
    • 0347456056 scopus 로고
    • Kathawala, F. G., Coppola, G. M., Schuster, H. F., Eds; Wiley: New York
    • See, e.g.: Sharpe, C. J.; Palmer, P. J.; Evans, D. E.; Brown, G. R.; King, G.; Shadholt, R. S.; Trigg, R. B.; Ward, R. J.; Ashford, A.; Ross, J. W. J. Med. Chem. 1972, 15, 523. Milligan, B.; Holt, L. A. J. Soc. Dyers Colour. 1978, 94, 352. Mathison, I. W.; Solomon, W. E. In Isoquinolines; Kathawala, F. G., Coppola, G. M., Schuster, H. F., Eds; Wiley: New York, 1990; Vol. 2, p 367.
    • (1990) Isoquinolines , vol.2 , pp. 367
    • Mathison, I.W.1    Solomon, W.E.2
  • 71
    • 84981945551 scopus 로고
    • Olah, G. A. Angew. Chem., Int. Ed. Engl. 1973, 12, 173; Angew. Chem. 1973, 85, 183. Olah, G. A. Carbocations and Electrophilic Reactions; Verlag Chemie: Weinheim, New York, 1974.
    • (1973) Angew. Chem., Int. Ed. Engl. , vol.12 , pp. 173
    • Olah, G.A.1
  • 72
    • 84981945551 scopus 로고
    • Olah, G. A. Angew. Chem., Int. Ed. Engl. 1973, 12, 173; Angew. Chem. 1973, 85, 183. Olah, G. A. Carbocations and Electrophilic Reactions; Verlag Chemie: Weinheim, New York, 1974.
    • (1973) Angew. Chem. , vol.85 , pp. 183
  • 73
    • 84981945551 scopus 로고
    • Verlag Chemie: Weinheim, New York
    • Olah, G. A. Angew. Chem., Int. Ed. Engl. 1973, 12, 173; Angew. Chem. 1973, 85, 183. Olah, G. A. Carbocations and Electrophilic Reactions; Verlag Chemie: Weinheim, New York, 1974.
    • (1974) Carbocations and Electrophilic Reactions
    • Olah, G.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.