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Total Synthesis and Structure-Activity Investigation of the Marine Natural Product Neopeltolide

The total synthesis and biological evaluation of neopeltolide and analogs are reported. The key bond-forming step utilizes a Lewis acid-catalyzed intramolecular macrocyclization that installs the tetrahydropyran ring and macrocycle simultaneously. Independent of each other, neither the macrolide nor...

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Detalhes bibliográficos
Main Authors: Custar, Daniel W., Zabawa, Thomas P., Hines, John, Crews, Craig M., Scheidt, Karl A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2735232/
https://ncbi.nlm.nih.gov/pubmed/19663512
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ja904604x
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