Mahboobi, Siavosh and Wiegrebe, Wolfgang and Popp, Alfred (1999) Synthesis of enantiomerically pure (-)-(S)-brevicolline. JOURNAL OF NATURAL PRODUCTS, 62 (4). pp. 577-579. ISSN 0163-3864,
Full text not available from this repository. (Request a copy)Abstract
(-)-(S)-Brevicolline (1) and related beta-carbolines were synthesized using an enantiomerically pure Michael-acceptor synthon (3). Subsequent Pictet-Spengler reaction afforded the tetrahydro-beta-carboline skeleton, which, in turn, was transformed to the beta-carboline by catalytic dehydrogenation.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | MARINE ORIGIN; |
| Subjects: | 600 Technology > 615 Pharmacy |
| Divisions: | Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 08 Nov 2022 14:06 |
| Last Modified: | 08 Nov 2022 14:06 |
| URI: | https://pred.uni-regensburg.de/id/eprint/48408 |
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