Abstract
New bicyclic aryloxypropynyl alcohols were prepared from stereoisomeric ketones of the phosphabicyclodecane series. Their steric structure was determined from the 1H and 13C NMR data. The stereochemistry of ethynylation of the bicyclic ketones was studied in relation to their structure.
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Logunov, A.P., Mukanova, M.S., Butin, B.M., and Erzhanov, K.B., Abstracts of Papers, Mezhdunarodnyi nauchnyi seminar “Perspektivy razvitiya khimii fosfora v XXI veke” (Int. Scientific Workshop “Prospects for the Development of Phosphorus Chemistry in the XXI Century”), Kokshetau-Almaty-Moscow, 2000, pp. 23–24.
Logunov, A.P., Mukanova, M.S., Erzhanov, K.B., and Butin, B.M., in Trudy Mezhdunarodnoi konferentsii “Sostoyanie i perspektivy razvitiya organicheskoi khimii v Respublike Kazakhstan” (Proc. Int. Conf. “State and Prospects for the Development of Organic Chemistry in the Republic of Kazakhstan”), Almaty-Shimkent, 2002, pp. 179–182.
Logunov, A.P., Mukanova, M.S., Butin, B.M., and Erzhanov, K.B., Zh. Obshch. Khim., 2002, vol. 72, no. 3, p. 469.
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Original Russian Text © M.S. Mukanova, A.P. Logunov, B.M. Butin, K.B. Erzhanov, 2006, published in Zhurnal Obshchei Khimii, 2006, Vol. 76, No. 2, pp. 224–228.
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Mukanova, M.S., Logunov, A.P., Butin, B.M. et al. Stereochemistry of aryloxypropynyl alcohols of the phosphabicyclodecane series. Russ J Gen Chem 76, 211–215 (2006). https://doi.org/10.1134/S1070363206020083
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DOI: https://doi.org/10.1134/S1070363206020083