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Rapid Access to Conformational Analogues of (+)-Peloruside A
[Image: see text] An efficient synthetic strategy for rapid access to analogues of peloruside A has been demonstrated. The synthetic route was highlighted by a simple esterification-based fragment coupling and a late stage ring-closing metathesis reaction. This convergent route has provided access t...
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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/PMC3272296/ https://ncbi.nlm.nih.gov/pubmed/22235754 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol203268t |
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