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   https://doi.org/10.1016/j.cub.2023.06.057  

   O’Banion, Bridget S; Jones, Piet; Demetros, Alexander A; Kelley, Brittni R; Knoor, Leah H; Wagner, Andrew S; Chen, Jin-Gui; Muchero, Wellington; Reynolds, Todd B; Jacobson, Daniel; et al (August 2023, Current Biology)
2. Supramolecular traps for highly phosphorylated inositol sources of phosphorus

   https://doi.org/10.1039/C9CC09321D  

   Pramanik, Subhamay; Day, Victor W.; Bowman-James, Kristin (March 2020, Chemical Communications)

   Structurally elusive inositol hexakisphosphates have been trapped in host–guest sandwiches between two picolinamide macrocycles that remain intact in solution, aided by hydrogen bonds and electrostatic interactions. This first report of macrocyclic complexes of inositol hexakisphosphates provides structural insight to significant biosources of phosphorus that impact the global phosphorus cycle. 

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3. Ferrier Carbocyclization-Mediated Synthesis of Enantiopure Azido Inositol Analogues

   https://doi.org/10.1021/acs.joc.9b03064  

   Ausmus, Alex P.; Hogue, Maxwell; Snyder, Justin L.; Rundell, Sarah R.; Bednarz, Krestina M.; Banahene, Nicholas; Swarts, Benjamin M. (March 2020, The Journal of Organic Chemistry)
4. Liposome triggered content release through molecular recognition of inositol trisphosphate

   https://doi.org/10.1039/d2cc00951j  

   Bottcher, Sydney E.; Lou, Jinchao; Best, Michael D. (April 2022, Chemical Communications)

   A stimuli-responsive liposomal platform that is selectively activated by inositol 1,4,5-trisphosphate (IP 3 ) over eleven other phosphorylated metabolites is reported. Dye release assays validated dose-dependent release of both hydrophilic and hydrophobic cargo driven by IP 3 , showcasing the potential of this platform for triggered release and sensing applications. 

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5. Snapshots of “crystalline” salt-water solutions of inositol hexaphosphate conformers

   https://doi.org/10.1039/d0dt03775  

   Kaur, S.; Pramanik, S.; Day, V. W.; Bowman-James, K. (June 2021, Dalton transactions)

   null (Ed.)

   Supramolecular insight to intra- and inter-ionic interactions in two inositol hexaphosphate conformers as a function of pH was enabled by NMR and crystallographic studies. These findings also shed light on the complex interactive roles of extended salt-water arrays through the crystal “solution” lattice. 

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