Synthetic progress toward the marine natural product zamamiphidin A

An asymmetric synthetic approach to the octahydrofuro[3,4-b]pyridine framework of marine natural product zamamiphidin A has been described. The key steps include an asymmetric Michael addition of (R)-N-tert-butanesulfinyl imidate with enamidomalonate to install the C10 stereocenter, an intramolecula...

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Detalles Bibliográficos
Autores principales: Wang, Hao, Tian, Di, Meng, Zhaoxiang, Chen, Zhihao, Xue, Fei, Liu, Xiao-Yu, Song, Hao, Qin, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050630/
https://www.ncbi.nlm.nih.gov/pubmed/35496609
http://dx.doi.org/10.1039/d0ra01580f

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050630/
https://www.ncbi.nlm.nih.gov/pubmed/35496609
http://dx.doi.org/10.1039/d0ra01580f

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