AN ENANTIOSELECTIVE ACCESS TO THE (-)-TUBOTAIWINE SKELETON

DOI: 10.1016/S0040-4039(00)95539-4

Source and publish data:

Tetrahedron Letters p. 3573 - 3576 (1987)

Update date:2022-08-03

Topics:

Authors:

Legseir, Belgacem

Henin, Jacques

Massiot, Georges

Vercauteren, Joseph

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Article abstract of DOI:10.1016/S0040-4039(00)95539-4

An efficient induction of chirality is obtained when using α-phenylethylamine as a chiral starting material to produce in few steps the skeleton of anilinoacrylic indole alkaloids.Ring enlargement is described to produce the complete five-ring system of tubotaiwine.

Full text of DOI:10.1016/S0040-4039(00)95539-4

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