Synthesis of new diverse macrocycles from diol precursors |
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Authors: | Charlotte M. Madsen |
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Affiliation: | Department of Chemistry, Technical University of Denmark, Kemitorvet, Building 201, DK-2800 Kgs. Lyngby, Denmark |
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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. |
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Keywords: | Macrocyclization Cyclic esters Reductive amination Diversity-oriented synthesis |
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