Facile synthesis of two diastereomeric indolizidines corresponding to the postulated structure of alkaloid 5,9E-259B from a Bufonid toad (Melanophryniscus)
A short synthesis of the postulated structure for indolizidine alkaloid 259B with the hydrogens at C5 and C9 entgegen has been achieved with complete control of stereochemistry at C5. Both diastereoisomers at C8 were obtained, but neither proved to be the natural product. The comparison of the mass...
Main Authors: | Angela Nelson, H. Martin Garraffo, Thomas F. Spande, John W. Daly, Paul J. Stevenson |
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Format: | Article |
Language: | English |
Published: |
Beilstein-Institut
2008-01-01
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Series: | Beilstein Journal of Organic Chemistry |
Online Access: | https://doi.org/10.1186/1860-5397-4-6 |
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