Abstract
An efficient method for the synthesis of spiro[3.3]heptanes and spiro[3.4]octanes of various structures has been developed using cycloalumination of substituted methylidenecyclobutanes with Et3Al in the presence of Cp2ZrCl2. A possibility of transformation of the in situ formed spiroaluminacyclopentanes to the corresponding thiophanes, selenophanes, and cyclopentanols in high yields and selectivity has been demonstrated.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 926–932, May, 2009.
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D’yakonov, V.A., Trapeznikova, O.A., Ibragimov, A.G. et al. Synthesis and transformations of metallacycles. Russ Chem Bull 58, 948–954 (2009). https://doi.org/10.1007/s11172-009-0121-4
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DOI: https://doi.org/10.1007/s11172-009-0121-4