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Updated: Apr 30, 2026

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols
Published on: April 4, 2014
Synthetic and computational evaluation of regiodivergent epoxide opening for diol and polyol synthesis
Andreas Gansäuer1, Peter Karbaum, David Schmauch
1Kekulé-Institut für Organische Chemie und Biochemie, Universität Bonn, Gerhard Domagk Str. 1, 53121 Bonn (Germany), Fax: (+49) 0228-73-5683. andreas.gansaeuer@uni-bonn.de.
Abstract:
In a combined synthetic and computational study, the factors governing the selectivity of the titanocene(III)-catalyzed regiodivergent epoxide opening (REO) with Kagan's complex via electron transfer leading to derivatives of 1,2-, 1,3-, and 1,4-diols were investigated. In this manner, valuable building blocks for the synthesis of 1,3- and 1,4-diols were identified. The computational study provides crucial structural features and energies of the transition states of ring opening that are important for the design of more selective catalysts.
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