Project Details
Description
Chiral saturated carbacyclic and heterocyclic structures are very frequent fragments of many natural products of high interest. Unsymmetrically substituted aromatics or hetero-aromatics could serve as very reasonable starting materials for a variety of synthons in the field of natural product synthesis, if there were a method available to render the hydrogenation of the respective aromatic precursor to the wanted saturated cyclic compound enantioselective. Several different strategies to solve this hitherto untackled problem are being developed .
| Status | Finished |
|---|---|
| Effective start/end date | 1/01/95 → 31/01/02 |
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Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.
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Transfer Hydrogenation in Ionic Liquids under Microwave Irradiation
Berthold, H., Schotten, T. & Hönig, H., 2002, In: Synthesis. p. 1607-1610Research output: Contribution to journal › Article › peer-review
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Enantioselective Synthesis of Ethyl Nipecotinate Using Cinchona Modified Heterogeneous Catalysts
Blaser, H.-U., Hönig, H., Studer, M. & Wedemeyer-Exl, C., 1999, In: Journal of Molecular Catalysis A. 139, p. 253-257Research output: Contribution to journal › Article › peer-review
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Enzymatic Resolution of Biologically Active Precursors versus Asymmetric Induction in Heterogeneous Catalysis
Hönig, H., Rogi-Kohlenprath, R. & Weber, H., 1995, Chiral Reactions in Heterogeneaous Catalysis. New York: Plenum Publ. Corp., p. 135-139Research output: Chapter in Book/Report/Conference proceeding › Chapter