Reddy, Mullapudi Mohan’s team published research in ChemBioChem in 2021 | CAS: 1195-59-1

2,6-Pyridinedimethanol(cas: 1195-59-1) belongs to pyridine. The basicity and metallophilic high donor number of these π-deficient systems has long favored them as ligands in metal catalysis. The last decade saw pyridine assume a stronger role as functional group for directed C–H oxidation/activation.Application In Synthesis of 2,6-Pyridinedimethanol

Application In Synthesis of 2,6-PyridinedimethanolIn 2021 ,《A Universal Chemical Method for Rational Design of Protein-Based Nanoreactors》 appeared in ChemBioChem. The author of the article were Reddy, Mullapudi Mohan; Bathla, Punita; Sandanaraj, Britto S.. The article conveys some information:

Self-assembly of a monomeric protease to form a multi-subunit protein complex “”proteasome”” enables targeted protein degradation in living cells. Naturally occurring proteasomes serve as an inspiration and blueprint for the design of artificial protein-based nanoreactors. Here we disclose a general chem. strategy for the design of proteasome-like nanoreactors. Micelle-assisted protein labeling (MAPLab) technol. along with the N-terminal bioconjugation strategy is utilized for the synthesis of a well-defined monodisperse self-assembling semi-synthetic protease. The designed protein is programmed to self-assemble into a proteasome-like nanostructure which preserves the functional properties of native protease. In the experiment, the researchers used 2,6-Pyridinedimethanol(cas: 1195-59-1Application In Synthesis of 2,6-Pyridinedimethanol)

2,6-Pyridinedimethanol(cas: 1195-59-1) belongs to pyridine. The basicity and metallophilic high donor number of these π-deficient systems has long favored them as ligands in metal catalysis. The last decade saw pyridine assume a stronger role as functional group for directed C–H oxidation/activation.Application In Synthesis of 2,6-Pyridinedimethanol

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