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.
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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