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Volumn 65, Issue 19, 2000, Pages 6167-6172

Laser flash photolysis evidence for styryl radical cation cyclization in the SET-induced photorearrangement of a p-methoxy-substituted 2-phenylallyl phosphite

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ANTHRACENE DERIVATIVE; BIPHENYL DERIVATIVE; PHOSPHITE; PHOSPHONIC ACID DERIVATIVE;

EID: 0034703319     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0006775     Document Type: Article
Times cited : (20)

References (43)
  • 1
    • 0003176219 scopus 로고
    • Ganapathy, S.; Dockery, K. P.; Sopchik, A. E.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 8863. The stereochemistry at phosphorus for this rearrangement has recently been reported: Hager, D. C.; Sopchik, A. E.; Bentrude, W. G. J. Org. Chem. 2000, 65, 2778.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 8863
    • Ganapathy, S.1    Dockery, K.P.2    Sopchik, A.E.3    Bentrude, W.G.4
  • 2
    • 0034607837 scopus 로고    scopus 로고
    • Ganapathy, S.; Dockery, K. P.; Sopchik, A. E.; Bentrude, W. G. J. Am. Chem. Soc. 1993, 115, 8863. The stereochemistry at phosphorus for this rearrangement has recently been reported: Hager, D. C.; Sopchik, A. E.; Bentrude, W. G. J. Org. Chem. 2000, 65, 2778.
    • (2000) J. Org. Chem. , vol.65 , pp. 2778
    • Hager, D.C.1    Sopchik, A.E.2    Bentrude, W.G.3
  • 22
    • 0034607677 scopus 로고    scopus 로고
    • (d) Bentrude, W. G.; Lee, S.-G.; Akutagawa, K.; Ye, W.; Charbonnel, Y.; Omelanczuk, J. Phosphorus Sulfur 1987, 30, 105. The stereochemistry at phosphorus of this rearrangement has recently been reported: Hager, D. C.; Bentrude, W. G. J. Org. Chem. 2000, 65, 2786.
    • (2000) J. Org. Chem. , vol.65 , pp. 2786
    • Hager, D.C.1    Bentrude, W.G.2
  • 23
    • 0343778359 scopus 로고    scopus 로고
    • 6d,10 of alkene radical cations have been reported
    • 6d,10 of alkene radical cations have been reported.
  • 26
    • 0342907609 scopus 로고    scopus 로고
    • 13
    • 13
  • 32
    • 0011578436 scopus 로고
    • 1DCA* to generate biphenyl radical cation leads to a quantum yield of cage escape to give free radical ions of 0.83. The high yield is due to the fact that back electron transfer between biphenyl radical cation and cyanoaromatic sensitizer radical anions is sufficiently exergonic to fall in the Marcus inverted region and is thus much slower than is typical for more easily oxidized donors. Gould, I. R.; Ege, D.; Mattes, S. L.; Farid, S. J. Am. Chem. Soc. 1987, 109, 3794.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 3794
    • Gould, I.R.1    Ege, D.2    Mattes, S.L.3    Farid, S.4
  • 33
    • 0342907608 scopus 로고
    • Ph.D. Dissertation, University of Utah
    • Dockery, K. P. Ph.D. Dissertation, University of Utah, 1995.
    • (1995)
    • Dockery, K.P.1
  • 37
    • 0343778357 scopus 로고    scopus 로고
    • note
    • 8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.