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Total Synthesis and Structural Reassignment of Laingolide A
The asymmetric total synthesis of four diastereomers of laingolide A was achieved, which led to the unambiguous assignment of the stereochemistry of the natural product. The salient features of the convergent, fully stereocontrolled approach were a copper-catalysed stereospecific Kumada-type couplin...
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| Pubblicato in: | Mar Drugs |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8145716/ https://ncbi.nlm.nih.gov/pubmed/33925490 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/md19050247 |
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