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Stereoselective total synthesis and structural revision of the diacetylenic diol natural products strongylodiols H and I

The stereoselective total synthesis of strongylodiol H and I has been accomplished. The synthetic procedure comprised the stereoselective reduction of a ketone functionality in an ene–yne–one employing CBS as a catalyst and a Cadiot–Chodkiewicz coupling reaction as the key reaction steps. A common a...

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Detalles Bibliográficos
Autores principales:	Gangadhar, Pamarthi, Ramakrishna, Sayini, Venkateswarlu, Ponneri, Srihari, Pabbaraja
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Beilstein-Institut 2018
Materias:	Full Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142741/ https://www.ncbi.nlm.nih.gov/pubmed/30254695 http://dx.doi.org/10.3762/bjoc.14.206

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