Issue 23, 1970

General methods of alkaloid synthesis. A new approach to the synthesis of the 5,10b-ethanophenanthridine Amaryllidaceae alkaloids. The total synthesis of (±)-3-epi-elwesine

Abstract

Methyl vinyl ketone annelation of the Δ2- pyrroline (5b) prepared by acid-catalysed thermal rearrangement of the cyclopropyl imine (7) has been exploited in an efficient eight-step stereoselective total synthesis of racemic 3-epi-elwesine (3b).

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1585-1586

General methods of alkaloid synthesis. A new approach to the synthesis of the 5,10b-ethanophenanthridine Amaryllidaceae alkaloids. The total synthesis of (±)-3-epi-elwesine

R. V. Stevens and L. E. DuPree, J. Chem. Soc. D, 1970, 1585 DOI: 10.1039/C29700001585

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