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Volumn 62, Issue 7, 2006, Pages 1467-1473

Photooxygenations of 1-naphthols: An environmentally friendly access to 1,4-naphthoquinones

Author keywords

Green chemistry; Photochemistry; Photooxygenations; Quinones

Indexed keywords

1 NAPHTHOL DERIVATIVE; 1,4 NAPHTHOQUINONE DERIVATIVE; 1,5 NAPHTHALENEDIOL; 5 ACETAMIDO 1,4 NAPHTHOQUINONE; DYE; JUGLONE; NAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 30744437408     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.11.021     Document Type: Article
Times cited : (52)

References (62)
  • 35
    • 1442326812 scopus 로고    scopus 로고
    • For general overviews on 'Green Photochemistry', see: (a) A. Albini, and M. Fagnoni Green Chem. 6 2004 1
    • (2004) Green Chem. , vol.6 , pp. 1
    • Albini, A.1    Fagnoni, M.2
  • 39
  • 49
    • 30744463615 scopus 로고    scopus 로고
    • Radiation Chemistry Data Center
    • 2 lifetimes in various solvents, see the Radiation Chemistry Data Center: http://allen.rad.nd. edu/compilations/SingOx/table1/t1.htm.
  • 50
    • 30744469455 scopus 로고    scopus 로고
    • Unpublished results.
    • Much higher yields were obtained in acetone when quartz vessels were used and this phenomenon is currently investigated. Suchard, O.; Waske, P. A.; Mattay, J.; Oelgemöller M. Unpublished results.
    • Suchard, O.1    Waske, P.A.2    Mattay, J.3    Oelgemöller, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.