Koller, Stephan G. and Bauer, Jonathan O. and Strohmann, Carsten (2017) Selective Si-C(sp(3)) Bond Cleavage in (Aminomethyl)silanes by Carbanionic Nucleophiles and Its Stereochemical Course. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 56 (27). pp. 7991-7994. ISSN 1433-7851, 1521-3773
Full text not available from this repository. (Request a copy)Abstract
Selective cleavage of a silicon-carbon bond in tetraorganosilanes is still a great challenge. A new type of Si-C(sp(3)) bond cleavage in bench-stable (aminomethyl)silanes with common organolithium reagents as nucleophiles has now been identified. Suitable leaving groups are benzyl, allyl, and phenylthiomethyl groups. A beta-donor function and polar solvents are essential for the reaction. Simple switching between alpha-deprotonation and substitution is possible through slight modifications of the reaction conditions. The stereochemical course of the reaction was elucidated by using a silicon-chiral benzylsilane. The new transformation proceeds stereospecifically with inversion of configuration and can be used for the targeted synthesis of enantiomerically pure tetraorganosilanes, which are otherwise difficult to access. Quantum chemical calculations provided insight into the mechanism of the new substitution.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | CARBON-SILICON BOND; CROSS-COUPLING REACTIONS; ENANTIOSELECTIVE SYNTHESIS; ASYMMETRIC-SYNTHESIS; STEREOGENIC SILANES; CENTERED CHIRALITY; CRYSTAL-STRUCTURES; SI BOND; ARYL; REAGENTS; alkyllithium compounds; chirality; density functional calculations; nucleophilic substitution; silanes |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Anorganische Chemie |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 14 Dec 2018 13:10 |
| Last Modified: | 11 Feb 2019 13:13 |
| URI: | https://pred.uni-regensburg.de/id/eprint/674 |
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