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Synthesis of new diverse macrocycles from diol precursors
Authors:Charlotte M. Madsen
Affiliation:Department of Chemistry, Technical University of Denmark, Kemitorvet, Building 201, DK-2800 Kgs. Lyngby, Denmark
Abstract:
The formation of a library of diverse macrocycles with different ring sizes from two easily accessible building blocks is presented. Reacting diol precursors with electrophilic reagents lead to 17-membered sulfites and 19-membered malonates in 34-79% yield. Double-reductive amination of dialdehyde analogs of the diol precursors leads to 15-membered amines in yields ranging from 9 to 60%, reflecting large differences in reactivity based on steric environment.
Keywords:Macrocyclization   Cyclic esters   Reductive amination   Diversity-oriented synthesis
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