| Literature DB >> 26768697 |
Christiana Kitsiou1, Jordan J Hindes1, Phillip I'Anson1, Paula Jackson1, Thomas C Wilson1, Eleanor K Daly1, Hannah R Felstead1, Peter Hearnshaw1, William P Unsworth2.
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
Year: 2015 PMID: 26768697 DOI: 10.1002/anie.201509153
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336