The Synthesis of Structurally Diverse Macrocycles By Successive Ring Expansion

Angew Chem Int Ed Engl. 2015 Dec 21;54(52):15794-8. doi: 10.1002/anie.201509153. Epub 2015 Nov 13.

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.

Keywords: macrocycles; medium-sized rings; rearrangement; ring expansion; structural diversity.