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Volumn 72, Issue 25, 2007, Pages 9786-9789

Photoinduced C-Br homolysis of 2-bromobenzophenones and Pschorr ring closure of 2-aroylaryl radicals to fluorenones

Author keywords

[No Author keywords available]

Indexed keywords

BROMINE; CYCLIZATION; PHOTOCHEMICAL REACTIONS; STABILIZATION;

EID: 36849033921     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7017872     Document Type: Article
Times cited : (54)

References (20)
  • 2
    • 2942545129 scopus 로고    scopus 로고
    • Galli, C. Chem. Rev. 1988, 88, 765.
    • (b) Galli, C. Chem. Rev. 1988, 88, 765.
  • 17
    • 37049094616 scopus 로고    scopus 로고
    • Triplet energies are less likely to vary considerably for all ketones 3-8, see: Leigh, W. J.; Arnold, D. R. J. Chem. Soc., Chem. Commun. 1980, 406.
    • Triplet energies are less likely to vary considerably for all ketones 3-8, see: Leigh, W. J.; Arnold, D. R. J. Chem. Soc., Chem. Commun. 1980, 406.
  • 18
    • 0003804844 scopus 로고
    • State-switching for substituted benzophenones does not occur except for dialkylamino substituents, see:, Padwa, A, Ed, Marcel Dekker: New York, Ch. 4
    • State-switching for substituted benzophenones does not occur except for dialkylamino substituents, see: Wagner, P. J.; Park, B.-S. In Organic Photochemistry; Padwa, A., Ed.; Marcel Dekker: New York, 1991; Vol. II, Ch. 4.
    • (1991) Organic Photochemistry , vol.2
    • Wagner, P.J.1    Park, B.-S.2
  • 20
    • 36849031660 scopus 로고    scopus 로고
    • Preparative photolyses were run for an extended duration to maximize conversion of 2-bromoketones to products, as the products also absorb. Therefore, relative durations of irradiation should not be correlated with the reactivities of ketones.
    • Preparative photolyses were run for an extended duration to maximize conversion of 2-bromoketones to products, as the products also absorb. Therefore, relative durations of irradiation should not be correlated with the reactivities of ketones.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.