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Updated: Jul 10, 2026

A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
Published on: September 9, 2016
A total synthesis of galbonolide B
Philip J Parsons1, Lewis Pennicott, James Eshelby
1Department of Chemistry, The University of Sussex, Falmer, Brighton, UK. P.J.Parsons@sussex.ac.uk
Abstract:
An ester enolate rearrangement/silicon mediated fragmentation cascade was used to convert 7 and 8 into the alcohol 9. The alcohol 9 was converted into the allylic alcohol 12 and then to the ester 14. A further ester enolate rearrangement furnished the stereochemical identity of galbonolide B 1. Base mediated macrocyclization of the acetate ester 16 followed by base mediated alkylation and acetal deprotection gave galbonolide B 1.
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