Halogenoborane mediated allene cyclooligomerization

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Abstract

The halogenoboranes XB(C6F5)2 (X: Cl, Br) react with allene to give a mixture of the cyclotrimer 1,3,5-trimethylenecyclohexane (1) and the related halogenoborylated cyclotetramerization products 3a and 3b. Alkyl-substituted allenes were catalytically cyclotrimerized metal-free by XB(C6F5)2 (X: Cl, Br) to give cis,trans-2,4,6-trialkyl-1,3,5-trimethylenecyclohexanes under mild conditions.

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Tao, X., Wölke, C., Daniliuc, C. G., Kehr, G., & Erker, G. (2019). Halogenoborane mediated allene cyclooligomerization. Chemical Science, 10(8), 2478–2482. https://doi.org/10.1039/C8SC04790A

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