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Synthesis of (±)-trans-2,5-Diisopropylborolane
Department of Chemistry, University College Dublin, Belfield, Dublin 4, Ireland
* Author to whom correspondence should be addressed.
Received: 1 February 2001; in revised form: / Accepted: 3 February 2001 / Published: 28 February 2001
Abstract: The cyclic hydroboration of 2,7-dimethyl-2,6-octadiene (6) was studied. It was found that the stereochemical outcome of the reaction was dependent upon the solvent, temperature, time and the nature of the borane reagent. Pure racemic trans-2,5-diisopropylborolane (14) was isolated following selective complexation of the cis-2,5-diisopropylborolane (15) with 1-(2-hydroxyethyl)-pyrrolidine.
Keywords: Cyclic hydroboration; diisopropylborolane; complexation
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MDPI and ACS Style
Laschober, G.; Zorzi, M.; Hodgetts, K.J. Synthesis of (±)-trans-2,5-Diisopropylborolane. Molecules 2001, 6, 244-252.
Laschober G, Zorzi M, Hodgetts KJ. Synthesis of (±)-trans-2,5-Diisopropylborolane. Molecules. 2001; 6(3):244-252.
Laschober, Gerhard; Zorzi, Massimo; Hodgetts, Kevin J. 2001. "Synthesis of (±)-trans-2,5-Diisopropylborolane." Molecules 6, no. 3: 244-252.