Seitz, Michael and Reiser, Oliver (2005) Synthetic approaches towards structurally diverse gamma-butyrolactone natural-product-like compounds. CURRENT OPINION IN CHEMICAL BIOLOGY, 9 (3). pp. 285-292. ISSN 1367-5931, 1879-0402
Full text not available from this repository. (Request a copy)Abstract
Natural products containing a gamma-butyrolactone ring are abundant in nature; however, few general synthetic approaches to their stereoselective synthesis with broad structural variety are known. In this article, recent developments towards mono- and polycyclic gamma-butyrolactone natural products and analogs are discussed. A special focus is given to asymmetric methods applying transition metal or organocatalysts that allow not only the efficient introduction of a broad variety of functional groups but ideally also the flexible construction of various natural-product-like, polycyclic scaffolds from common precursors.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | ENANTIOSELECTIVE TOTAL-SYNTHESIS; STEREOSELECTIVE-SYNTHESIS; CATALYZED CYCLOCARBONYLATION; PARACONIC ACIDS; LACTONES; LIBRARIES; ALDEHYDES; KETONES; (+)-BLASTMYCINONE; DIAZOACETATES |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser |
| Depositing User: | Petra Gürster |
| Date Deposited: | 23 Mar 2022 07:51 |
| Last Modified: | 23 Mar 2022 07:51 |
| URI: | https://pred.uni-regensburg.de/id/eprint/36036 |
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