Abstract
Aromatic ring isosteres and rigidified saturated hydrocarbons are important motifs to enable drug discovery. Herein we disclose [2]-ladderanes as a class of meta-substituted aromatic ring isosteres and rigidified cyclohexanes. A straightforward synthesis of the building blocks is presented along with representative derivatization. Preliminary studies reveal that the [2]-ladderanes offer similar metabolic and physicochemical properties thus establishing this class of molecules as interesting motifs.
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CITATION STYLE
Epplin, R. C., Paul, S., Herter, L., Salome, C., Hancock, E. N., Larrow, J. F., … Brown, M. K. (2022). [2]-Ladderanes as isosteres for meta-substituted aromatic rings and rigidified cyclohexanes. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-33827-3
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