Analysis shows efficient methodologies for synthesizing organofluorine compounds, implying improved access to value-added products.
The discovery of convenient and efficient methodologies for preparing optically active organofluorine compounds has received much attention from the synthetic community. Herein, we report an organoiodine-catalyzed desymmetric fluorolactonization of α,α-diallylcarboxylic acids in the presence of Et₃N·3HF and Selectfluor, providing a straightforward access to value-added chiral α-quaternary fluorinated lactone. The reaction features moderate to good yields and broad functional group compatibility. Notably, the development of novel chiral organoiodine catalysts promotes the enantio- and diastereoselective fluorolactonization of aliphatic alkenes for the first time.
No takes yet. Share an insight, caveat, or question.
Chen et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: