Photochemical reactions of cyclopropyl ketones by electron transfer

Schmoldt P, Kirschberg T, Fagnoni M, Mattay J (1998)
JOURNAL OF INFORMATION RECORDING 24(3-4): 249-252.

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Abstract
Photoinduced electron transfer (PET) from triethylamine (TEA) to cyclopropyl ketones initiated a cyclopropylcarbinyl-homoallyl rearrangement. Attack of the so formed homoallyl radicals on a terminally unsaturated side chain gave various bicyclic products the structure of which depends on the position and length of that side chain.
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Schmoldt P, Kirschberg T, Fagnoni M, Mattay J. Photochemical reactions of cyclopropyl ketones by electron transfer. JOURNAL OF INFORMATION RECORDING. 1998;24(3-4):249-252.
Schmoldt, P., Kirschberg, T., Fagnoni, M., & Mattay, J. (1998). Photochemical reactions of cyclopropyl ketones by electron transfer. JOURNAL OF INFORMATION RECORDING, 24(3-4), 249-252.
Schmoldt, P., Kirschberg, T., Fagnoni, M., and Mattay, J. (1998). Photochemical reactions of cyclopropyl ketones by electron transfer. JOURNAL OF INFORMATION RECORDING 24, 249-252.
Schmoldt, P., et al., 1998. Photochemical reactions of cyclopropyl ketones by electron transfer. JOURNAL OF INFORMATION RECORDING, 24(3-4), p 249-252.
P. Schmoldt, et al., “Photochemical reactions of cyclopropyl ketones by electron transfer”, JOURNAL OF INFORMATION RECORDING, vol. 24, 1998, pp. 249-252.
Schmoldt, P., Kirschberg, T., Fagnoni, M., Mattay, J.: Photochemical reactions of cyclopropyl ketones by electron transfer. JOURNAL OF INFORMATION RECORDING. 24, 249-252 (1998).
Schmoldt, P, Kirschberg, T, Fagnoni, M, and Mattay, Jochen. “Photochemical reactions of cyclopropyl ketones by electron transfer”. JOURNAL OF INFORMATION RECORDING 24.3-4 (1998): 249-252.
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