Enantioselective synthesis of the gibbane framework

Seiichi Takano, Chiyoshi Kasahara, Kunio Ogasawara

Journal of the Chemical Society Chemical Communications · 1981 · 22 citations · 0 references

Concepts

Abstract

The triketone (1), possessing a mirror plane of symmetry, prepared from indane-1,3-dione, has been transformed into the gibbane framework enantioselectively by asymmetric aldolization catalysed by L-proline.