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Updated: Jun 10, 2026

A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
Published on: September 9, 2016
Stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin
Ahmed M Zaed1, Andrew Sutherland
1WestCHEM, Department of Chemistry, The Joseph Black Building, University of Glasgow, Glasgow, UKG12 8QQ.
Abstract:
A new approach for the stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin has been developed using a palladium(ii)-catalysed MOM-ether directed Overman rearrangement to establish the second stereogenic centre and a cross metathesis reaction to generate the carbon backbone. In the final stage, a one-pot acid mediated deprotection of aldehyde, guanidine and hydroxyl groups gave an intermediate that underwent facile cyclisation to (+)-monanchorin.
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