Abstract
The reaction of 1,2-dibromoethane with α-carbanions of lithium acylates generated from acetic, butyric, isobutyric, and capronic acids with lithium diisopropylamide has been studied. Anion-radical and anionic pathways of the products formation have been discussed.
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Original Russian Text © A.V. Zorin, A.T. Zaynashev, A.R. Chanysheva, V.V. Zorin, 2015, published in Zhurnal Obshchei Khimii, 2015, Vol. 85, No. 6, pp. 914–917.
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Zorin, A.V., Zaynashev, A.T., Chanysheva, A.R. et al. Reaction of α-carbanions of lithium acylates with 1,2-dibromoethane. Russ J Gen Chem 85, 1382–1385 (2015). https://doi.org/10.1134/S1070363215060043
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DOI: https://doi.org/10.1134/S1070363215060043