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Expedient Enantioselective Synthesis of Cermizine D
[Image: see text] An efficient enantioselective synthesis of cermizine D has been developed that exploits the use of a common intermediate to access over 85% of the carbon backbone. Key steps include an organocatalyzed heteroatom Michael addition, a diastereoselective alkylation with α-iodomethyl ph...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3319147/ https://ncbi.nlm.nih.gov/pubmed/22372610 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol300342n |
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