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Regioselectivity in the Ring Opening of Epoxides for the Synthesis of Aminocyclitols from D-(−)-Quinic Acid

Efficient syntheses of four aminocyclitols are reported. Each synthesis is accomplished in eight steps starting from D-(−)-quinic acid. The key step involves a highly regioselective ring opening of epoxides by sodium azide.

Detalles Bibliográficos
Autores principales:	Shih, Tzenge-Lien, Yang, Shu-Yu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2012
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268476/ https://www.ncbi.nlm.nih.gov/pubmed/22508330 http://dx.doi.org/10.3390/molecules17044498

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