Studies on the total synthesis of the saponaceolides. 2. Enantioselective synthesis of 2-epi-saponaceolide B

DOI: 10.1016/S0040-4039(99)00367-6

Source and publish data:

Tetrahedron Letters p. 3067 - 3070 (1999)

Update date:2022-08-04

Topics:

Authors:

Vidari, Giovanni

Pazzi, Natalina

Lanfranchi, Gianluigi

Serra, Stefano

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Article abstract of DOI:10.1016/S0040-4039(99)00367-6

The paper describes an asymmetric convergent synthesis of 2-epi- saponaceolide B, illustrating a general approach to the construction of the saponaceolide structure. The strategic C10'-C11' bond was formed by coupling a lithium salt containing the left pa

Full text of DOI:10.1016/S0040-4039(99)00367-6

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