Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction"

Schiel C, Oelgemoller M, Mattay J (2001)
SYNTHESIS-STUTTGART (8): 1275-1279.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Abstract / Bemerkung
Irradiation of substituted 1,4-benzo- or 1,4-naphthoquinones in the presence of several aldehydes resulted in the formation of acylated hydroquinones in good yields. In the case of 5-acetyloxy naphthoquinone 8, both regioisomers were formed, but the 2,8-isomer was favored in all cases examined. Even acylated tetrahydroxy naphthalenes became available in good yields by this method.
Erscheinungsjahr
Zeitschriftentitel
SYNTHESIS-STUTTGART
Zeitschriftennummer
8
Seite
1275-1279
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PUB-ID

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Schiel C, Oelgemoller M, Mattay J. Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction". SYNTHESIS-STUTTGART. 2001;(8):1275-1279.
Schiel, C., Oelgemoller, M., & Mattay, J. (2001). Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction". SYNTHESIS-STUTTGART(8), 1275-1279.
Schiel, C., Oelgemoller, M., and Mattay, J. (2001). Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction". SYNTHESIS-STUTTGART, 1275-1279.
Schiel, C., Oelgemoller, M., & Mattay, J., 2001. Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction". SYNTHESIS-STUTTGART, (8), p 1275-1279.
C. Schiel, M. Oelgemoller, and J. Mattay, “Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction"”, SYNTHESIS-STUTTGART, 2001, pp. 1275-1279.
Schiel, C., Oelgemoller, M., Mattay, J.: Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction". SYNTHESIS-STUTTGART. 1275-1279 (2001).
Schiel, C, Oelgemoller, M, and Mattay, Jochen. “Photoacylation of electron-rich quinones: An application of the "photo-Friedel-Crafts reaction"”. SYNTHESIS-STUTTGART 8 (2001): 1275-1279.