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Studies Towards the Synthesis of Amphidinolide C1: Stereoselective Construction of the C(1) – C(15) Segment
An enantioselective synthesis of the C(1)–C(15) segment of the marine natural product amphidinolide C has been accomplished by a route that includes a stereoselective boron-Wittig reaction to furnish a trisubstituted alkenylboronate. In addition, the route employs enantioselective alkene diboration...
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| Publicado no: | Org Lett |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7982962/ https://ncbi.nlm.nih.gov/pubmed/33180502 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.0c03134 |
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