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Collect. Czech. Chem. Commun. 1989, 54, 3284-3293
https://doi.org/10.1135/cccc19893284

The hydroalumination-iodination of enyne α-alcohols: Synthesis of 3-methyl-2,4-alkadien-1-ols

Ashot P. Khrimyana, Oganes A. Gharibyana, Ludvík Streinzb, Zdeněk Wimmerb, Miroslav Romaňukb and Shaliko O. Badanyana

a Institute of Organic Chemistry, Armenian Academy of Sciences, 375 094 Yerevan, U.S.S.R.
b Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6, Czechoslovakia

Crossref Cited-by Linking

  • Gubbels Matthew A., Hulce Martin, Kum John M., Urick Andrew K., Villa Eric M.: Stereoselective synthesis of exocyclic allenes by double hydride reduction of 3-alkynyl-2-cycloalkenones. Tetrahedron 2016, 72, 6052. <https://doi.org/10.1016/j.tet.2016.07.058>
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  • KHRIMYAN A. P., GARIBYAN O. A., STREINZ L., WIMMER Z., ROMANUK M., BADANYAN SH. O.: ChemInform Abstract: Hydroalumination‐Iodination of Enyne α‐Alcohols: Synthesis of 3‐Methyl‐2,4‐alkadien‐1‐ols. ChemInform 1990, 21. <https://doi.org/10.1002/chin.199012106>