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Asymmetric Total Synthesis and Absolute Stereochemistry of the Neuroactive Marine Macrolide Palmyrolide A()

[Image: see text] The first asymmetric total synthesis and determination of the absolute configuration for the neuroactive marine macrolide Palmyrolide A is described. The highlight of the synthesis is macrocyclization via trans-enamide formation catalyzed by copper (I) iodide and cesium carbonate....

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Detaylı Bibliyografya
Asıl Yazarlar: Tello-Aburto, Rodolfo, Johnson, Emily M., Valdez, Cheyenne K., Maio, William A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2012
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3352666/
https://ncbi.nlm.nih.gov/pubmed/22475318
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol300673m
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