1286023-30-0Relevant academic research and scientific papers
Accelerated SuFEx Click Chemistry For Modular Synthesis**
Barrow, Andrew S.,Gialelis, Timothy L.,Homer, Joshua A.,Koelln, Rebecca A.,Moses, John E.,Smedley, Christopher J.
supporting information, (2021/12/10)
SuFEx click chemistry is a powerful method designed for the selective, rapid, and modular synthesis of functional molecules. Classical SuFEx reactions form stable S?O linkages upon exchange of S?F bonds with aryl silyl-ether substrates, and while near-per
Quantum Dot-Catalyzed Photoreductive Removal of Sulfonyl-Based Protecting Groups
Perez, Kaitlyn A.,Rogers, Cameron R.,Weiss, Emily A.
supporting information, p. 14091 - 14095 (2020/06/08)
This Communication describes the use of CuInS2/ZnS quantum dots (QDs) as photocatalysts for the reductive deprotection of aryl sulfonyl-protected phenols. For a series of aryl sulfonates with electron-withdrawing substituents, the rate of deprotection for the corresponding phenyl aryl sulfonates increases with decreasing electrochemical potential for the two electron transfers within the catalytic cycle. The rate of deprotection for a substrate that contains a carboxylic acid, a known QD-binding group, is accelerated by more than a factor of ten from that expected from the electrochemical potential for the transformation, a result that suggests that formation of metastable electron donor–acceptor complexes provides a significant kinetic advantage. This deprotection method does not perturb the common NHBoc or toluenesulfonyl protecting groups and, as demonstrated with an estrone substrate, does not perturb proximate ketones, which are generally vulnerable to many chemical reduction methods used for this class of reactions.
