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Synthesis of (1E)-1-Chloroalk-1-en-4-ynes

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Abstract

A stereoselective method has been developed for the synthesis of (1E)-chloroalk-1-en-4-ynes, promising precursors to 1,4-enynes, on the basis of alkynylation of (E)-1,3-dichloropropene in the presence of copper(I) iodide and tetrabutylammonium bromide.

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Authors and Affiliations

  1. Ufa State Petroleum Technological University, 450062, Ufa, Russia

    R. N. Shakhmaev, M. G. Ignatishina & V. V. Zorin

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  1. R. N. Shakhmaev
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  2. M. G. Ignatishina
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  3. V. V. Zorin
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Correspondence to R. N. Shakhmaev.

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Shakhmaev, R.N., Ignatishina, M.G. & Zorin, V.V. Synthesis of (1E)-1-Chloroalk-1-en-4-ynes. Russ J Gen Chem 90, 1365–1367 (2020). https://doi.org/10.1134/S1070363220070270

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