Cedric J. Stress; Basilius Sauter; Lukas A. Schneider; Timothy Sharpe; Dennis Gillingham
Angew. Chem. Int. Ed. Engl., 2019, 58(28), 9570-9574
https://doi.org/10.1002/anie.201902513

Abstract

Herein we perform a seven-step chemical synthesis of a DNA-encoded macrocycle library (DEML) on DNA. Inspired by polyketide and mixed peptide-polyketide natural products, the library was designed to incorporate rich backbone diversity. Achieving this diversity, however, comes at the cost of custom synthesis of bifunctional building block libraries. Our work outlines the importance of careful retrosynthetic design in DNA-encoded libraries, while revealing areas where new DNA synthetic methods are needed.