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Updated: Apr 26, 2026

Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
Synthetic studies on lemonomycin: construction of the tetracyclic core
Alberto Jiménez-Somarribas1, Robert M Williams2
1Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523-1872, United States.
Abstract:
A substrate-induced stereocontrol strategy was used to gain access to the tetracyclic core of (-)-lemonomycin. An advanced intermediate was prepared from a known substituted tyrosinol through a 16-step sequence, which involved a Pictet-Spengler reaction, a [3+2] dipolar cycloaddition and an enamide hydrogenation.
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