Royal Society of Chemistry, Organic and Biomolecular Chemistry, 16(20), p. 3263-3267, 2022
DOI: 10.1039/d2ob00498d
Full text: Unavailable
The synthesis of α-fluoroamines was achieved via deoxygenative geminal fluorosulfonimidation of 1,2-diketones using a dealkylation-resistant phosphoramidite under mild conditions that require neither excess reagents nor transition metal catalysts.