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Stereoselective Total Synthesis of (−)-Cleistenolide
[Image: see text] A facile stereoselective total synthesis of cleistenolide (1) from natural chiral template D-arabinose has been achieved in eight steps and 49% overall yield, employing key steps including, Wittig olefination, selective 1,3-trans-acetal formation, and modified Yamaguchi esterificat...
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| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2921661/ https://ncbi.nlm.nih.gov/pubmed/20704451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo101059e |
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