Abstract
The reaction of car-3-ene-2,5-dione (1), an oxidation product of (+)-car-3-ene, with lithium acetylides proceeds stereospecifically, but not regioselectively, to give only mixtures of regioisomeric acetylenic alcohols with thesyn-orientation of the hydroxy group.
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Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 183–185, January, 1998.
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Galin, F.Z., Kashina, Y.A., Zainullin, R.A. et al. Reaction of lithium acetylides with car-3-ene-2,5-dione. Russ Chem Bull 47, 185–186 (1998). https://doi.org/10.1007/BF02495533
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DOI: https://doi.org/10.1007/BF02495533