Angewandte Chemie · 2015 · 33 citations · 67 references
PharmacyMedicinal ChemistryCombinatorial ChemistryDrug DiscoverySynthetic Medicinal ChemistryCombinatorial SynthesisDiversity-oriented SynthesisHeterocycle SynthesisMacrocycle SynthesisOrganic SynthesisRetrosynthetic AnalysisHeterocycle DiversificationMacrocycle DiversificationMacrocycle Library SynthesisMacrocycle Scaffold DesignMacrocyclic Library SynthesisRegioselective MacrocyclizationRing System DiversificationRing-forming Reactions
Abstract Structurally diverse macrocycles and medium‐sized rings (9–24 membered scaffolds, 22 examples) can be generated through a telescoped acylation/ring‐expansion sequence, leading to the insertion of linear fragments into cyclic β‐ketoesters without performing a discrete macrocyclization step. The key β‐ketoester motif is regenerated in the ring‐expanded product, meaning that the same sequence of steps can then be repeated (in theory indefinitely) with other linear fragments, allowing macrocycles with precise substitution patterns to be “grown” from smaller rings using the successive ring‐expansion (SuRE) method.
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DNA-Templated Organic Synthesis and Selection of a Library of Macrocycles
Zev J. Gartner, Brian N. Tse, Rozalina Grubina et al. · Science · 2004 · 516 citations · Full text
Elizabeth A. Villar, Dmitri Beglov, Spandan Chennamadhavuni et al. · Nature Chemical Biology · 2014 · 403 citations
David R. Spring · Organic & Biomolecular Chemistry · 2003 · 337 citations