4.8 Article

Reversible-irreversible approach to Schiff base macrocycles: Access to isomeric macrocycles with multiple salphen pockets

Journal

ORGANIC LETTERS
Volume 10, Issue 6, Pages 1255-1258

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol8001317

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We have developed methodology for the formation of a new family of metal-free Schiff base macrocycles utilizing the differential exchange rates of aldimines and ketimines. The more robust ketimine bond is kinetically inert under the milder conditions used for aldimine bond formation. In particular, this route enables access to the first conjugated macrocycles with four unsymmetrical N2O2 salphen-like pockets.

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