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Formal and total synthesis of (±)-cycloclavine
A ring fragmentation and intramolecular azomethine ylide 1,3-dipolar cycloaddition sequence of reactions was successfully used in the preparation of a known (±)-cycloclavine precursor in good overall yield. Results of efforts to incorporate the tetrasubstituted cyclopropane ring present in cycloclav...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3915717/ https://ncbi.nlm.nih.gov/pubmed/24511164 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2013.10.152 |
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