Diastereoselective formal synthesis of the antifungal agent, (+)- Preussin. A new entry to chiral pyrrolidines

Pedro De Armas; Fernando García-Tellado; José J. Marrero-Tellado; Juana Robles

doi:10.1016/S0040-4039(97)10468-3

Diastereoselective formal synthesis of the antifungal agent, (+)- Preussin. A new entry to chiral pyrrolidines

Pedro De Armas, Fernando García-Tellado, José J. Marrero-Tellado, Juana Robles

Producción científica: Contribución a una revista › Artículo › revisión exhaustiva

33 Citas (Scopus)

Resumen

A formal total synthesis of (+)-Preussin was achieved by using D- mannose as the starting material. The key step involved diastereoselective addition of allyltrimethylsilane to the bicyclic ketal 5.

Idioma original	Inglés
Páginas (desde-hasta)	131-134
Número de páginas	4
Publicación	Tetrahedron Letters
Volumen	39
N.º	1-2
DOI	https://doi.org/10.1016/S0040-4039(97)10468-3
Estado	Publicada - 1 ene. 1998
Publicado de forma externa	Sí

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title = "Diastereoselective formal synthesis of the antifungal agent, (+)- Preussin. A new entry to chiral pyrrolidines",

abstract = "A formal total synthesis of (+)-Preussin was achieved by using D- mannose as the starting material. The key step involved diastereoselective addition of allyltrimethylsilane to the bicyclic ketal 5.",

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AU - Marrero-Tellado, José J.

AU - Robles, Juana

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AB - A formal total synthesis of (+)-Preussin was achieved by using D- mannose as the starting material. The key step involved diastereoselective addition of allyltrimethylsilane to the bicyclic ketal 5.

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U2 - 10.1016/S0040-4039(97)10468-3

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Diastereoselective formal synthesis of the antifungal agent, (+)- Preussin. A new entry to chiral pyrrolidines

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