Issue 76, 2016

Formal total synthesis of (±)-strictamine – the [2,3]-Stevens rearrangement for construction of octahydro-2H-2,8-methanoquinolizines

Abstract

For decades, akuammiline alkaloids have attracted synthetic chemists due to their intriguing molecular architecture. Among the different structural elements embedded in their carboskeleton, the methanoquinolizidine system constitutes the signature structural element of this alkaloid family. Herein, we describe a novel synthetic access to this system which relies on a [2,3]-Stevens rearrangement and results in the formal synthesis of strictamine.

Graphical abstract: Formal total synthesis of (±)-strictamine – the [2,3]-Stevens rearrangement for construction of octahydro-2H-2,8-methanoquinolizines

Supplementary files

Article information

Article type
Communication
Submitted
25 Jul 2016
Accepted
16 Aug 2016
First published
16 Aug 2016
This article is Open Access
Creative Commons BY license

Chem. Commun., 2016,52, 11363-11365

Formal total synthesis of (±)-strictamine – the [2,3]-Stevens rearrangement for construction of octahydro-2H-2,8-methanoquinolizines

R. Eckermann, M. Breunig and T. Gaich, Chem. Commun., 2016, 52, 11363 DOI: 10.1039/C6CC06125G

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