메뉴 건너뛰기




Volumn 2002, Issue 2, 2002, Pages 109-122

Electron transfer vs. heterolytic reactions. Behaviour of N-benzylaziridine towards (aqua)xCuII and batho2CuII ions

Author keywords

Aziridines; Cyclen; Electron transfer; Heterolytic reactions; Radical cations

Indexed keywords

2,9 DIMETHYL 4,7 DIPHENYL 1,10 PHENANTHROLINEDISULFONATE COPPER; AZIRIDINE DERIVATIVE; BENZYL DERIVATIVE; COPPER DERIVATIVE; DIBENZYLPIPERAZINE; N BENZYLAZIRIDINE; PIPERAZINE DERIVATIVE; TETRABENZYLCYCLEN; UNCLASSIFIED DRUG;

EID: 3242806034     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (48)
  • 5
    • 0011053661 scopus 로고
    • Dick, C.R. J. Org. Chem., 1967, 32, 72 and 1970, 35, 3950.
    • (1970) J. Org. Chem. , vol.35 , pp. 3950
  • 8
  • 9
    • 3242756411 scopus 로고    scopus 로고
    • For a survey of literature data on the oxidation of aziridines see ref. 3
    • For a survey of literature data on the oxidation of aziridines see ref. 3.
  • 16
    • 0000057077 scopus 로고
    • Such a possibility was only suggested in a footnote, but no experimental details were ever presented in order to support it; see Kossai, R.; Simonet, J.; Dauphin, G. Tetrahedron Lett., 1980, 21, 3575.
    • (1980) Tetrahedron Lett. , vol.21 , pp. 3575
    • Kossai, R.1    Simonet, J.2    Dauphin, G.3
  • 23
    • 3242797959 scopus 로고    scopus 로고
    • Work in progress
    • Work in progress.
  • 24
    • 3242773507 scopus 로고    scopus 로고
    • note
    • v) are in the same order (9.10 and 8.47 eV, respectively).
  • 28
    • 3242760429 scopus 로고    scopus 로고
    • Both 2 and 3 are more easily oxidizable than 1; see ref. 2
    • Both 2 and 3 are more easily oxidizable than 1; see ref. 2.
  • 31
    • 0000749388 scopus 로고
    • Rozeboom, M.D.; Houk, K.N.; Searles, S.; Seyedrezai, S.E. J. Am. Chem. Soc., 1982, 104, 3448. The N-unsubstituted aziridines have lower values (cf. Lamaty, G.; Sanchez, J.-Y.; Sivade, A.; Wylde, J. Bull. Soc. Chim. France, 1985, 1261).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 3448
    • Rozeboom, M.D.1    Houk, K.N.2    Searles, S.3    Seyedrezai, S.E.4
  • 32
    • 0000749388 scopus 로고
    • Rozeboom, M.D.; Houk, K.N.; Searles, S.; Seyedrezai, S.E. J. Am. Chem. Soc., 1982, 104, 3448. The N-unsubstituted aziridines have lower values (cf. Lamaty, G.; Sanchez, J.-Y.; Sivade, A.; Wylde, J. Bull. Soc. Chim. France, 1985, 1261).
    • (1985) Bull. Soc. Chim. France , pp. 1261
    • Lamaty, G.1    Sanchez, J.-Y.2    Sivade, A.3    Wylde, J.4
  • 36
    • 3242761215 scopus 로고    scopus 로고
    • See ref. 2 and literature therein reported
    • See ref. 2 and literature therein reported.
  • 37
  • 41
    • 3242761216 scopus 로고
    • -1 were determined [a) Kodama, M.; Kimura, E. J. Chem. Soc., Dalton Trans., 1977, 2269 and 1978, 1083;
    • (1978) J. Chem. Soc., Dalton Trans. , pp. 1083
  • 43
    • 3242759606 scopus 로고    scopus 로고
    • Clay, R.M.; McCormac, H.
    • c) Clay, R.M.; McCormac, H.;
  • 48
    • 3242800251 scopus 로고    scopus 로고
    • note
    • 3 solution, but attempts to quantify them by NMR gave irreproducible results, due to uncontrollable losses during the evaporation process. Both compounds can be precisely determined using the gas chromatographic method.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.