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Updated: Feb 9, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
Published on: February 6, 2020
Total Synthesis of (+)-Guadinomic Acid via Hydroxyl-Directed Guanidylation
Bradley T Reid1, Artur K Mailyan1, Armen Zakarian1
1Department of Chemistry and Biochemistry , University of California , Santa Barbara , California 93110 , United States.
Abstract:
Protecting-group-free total synthesis of (+)-guadinomic acid is reported using δ-valerolactone as a readily available starting material. The protocol utilizes the recent hydroxyl-directed guanidylation of unactivated alkenes as an approach for direct stereoselective incorporation of the guanidine unit furnishing the natural product in 7 steps.
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