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Enantioselective Total Synthesis of (−)-Citrinadin A and Revision of its Stereochemical Structure
The first enantioselective total synthesis of (−)-citrinadin A has been accomplished in 20 steps from commercially available materials via an approach that minimizes refunctionalization and protection/deprotection operations. The cornerstone of this synthesis features an asymmetric vinylogous Mannic...
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| Главные авторы: | , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2013
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3748604/ https://ncbi.nlm.nih.gov/pubmed/23837457 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja405547f |
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