“…The reactions were studied on the example of symmetrical cyclic diynes, cyclododeca 1,7 diyne (1a), cyclotetradeca 1,8 diyne (1b), and cyclohexadeca 1,9 diyne (1c). 23 Herein, based on the results obtained previously on cycloalumination of disubstituted acetylenes, 3 we devel oped conditions (cycloalkadiyne : Et 3 Al : [Zr] = 1 : 6 : 0.1, 20-22 °C, hexane, 6 h) for cycloalumination of cyclotet radeca 1,8 diyne (1b) as a model compound. Under these conditions, 1b underwent cycloalumination involving both triple bonds to give isomeric tricyclic bisaluminacyclo pentenes 2b and 3b in the ratio of 1 : 1 in 91% total yield (Scheme 2).…”