Studies on the total synthesis of the saponaceolides. 1. Enantioselective synthesis of the spiroketal subunit

DOI: 10.1016/S0040-4039(99)00366-4

Source and publish data:

Tetrahedron Letters p. 3063 - 3066 (1999)

Update date:2022-08-03

Topics:

Authors:

Vidari, Giovanni

Lanfranchi, Gianluigi

Pazzi, Natalina

Serra, Stefano

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Article abstract of DOI:10.1016/S0040-4039(99)00366-4

An asymmetric synthesis of the tricyclic Spiroketal subunit of the saponaceolides is described in which the absolute stereochemistry at C-2' and C-6' is established through a conformationally and stereoelectronically controlled cyclization of a dihydroxyk

Full text of DOI:10.1016/S0040-4039(99)00366-4

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