Regioselective photoacylation of substituted naphthoquinones

Schiel C, Oelgemoller M, Mattay J (1998)
JOURNAL OF INFORMATION RECORDING 24(3-4): 257-260.

Journal Article | Published | English

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Abstract
Photoreactions of aldehydes with quinones exhibit acylated hydroquinones in good yields. In the case of substituted naphthoquinones (pos. 5-8) two regioisomers are formed. However, lithium perchlorate as additive affords only one regioisomer. This effect is discussed on the basis of semiempirical calculations.
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Schiel C, Oelgemoller M, Mattay J. Regioselective photoacylation of substituted naphthoquinones. JOURNAL OF INFORMATION RECORDING. 1998;24(3-4):257-260.
Schiel, C., Oelgemoller, M., & Mattay, J. (1998). Regioselective photoacylation of substituted naphthoquinones. JOURNAL OF INFORMATION RECORDING, 24(3-4), 257-260.
Schiel, C., Oelgemoller, M., and Mattay, J. (1998). Regioselective photoacylation of substituted naphthoquinones. JOURNAL OF INFORMATION RECORDING 24, 257-260.
Schiel, C., Oelgemoller, M., & Mattay, J., 1998. Regioselective photoacylation of substituted naphthoquinones. JOURNAL OF INFORMATION RECORDING, 24(3-4), p 257-260.
C. Schiel, M. Oelgemoller, and J. Mattay, “Regioselective photoacylation of substituted naphthoquinones”, JOURNAL OF INFORMATION RECORDING, vol. 24, 1998, pp. 257-260.
Schiel, C., Oelgemoller, M., Mattay, J.: Regioselective photoacylation of substituted naphthoquinones. JOURNAL OF INFORMATION RECORDING. 24, 257-260 (1998).
Schiel, C, Oelgemoller, M, and Mattay, Jochen. “Regioselective photoacylation of substituted naphthoquinones”. JOURNAL OF INFORMATION RECORDING 24.3-4 (1998): 257-260.
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