Regio- and stereochemical stability induced by anomeric and gauche effects in difluorinated pyrrolidines

• Ana Flávia Candida Silva,
• Francisco A. Martins and
• Matheus P. Freitas

Beilstein J. Org. Chem. 2024, 20, 1572–1579, doi:10.3762/bjoc.20.140

• N–H bond was the most stable conformer, allowing for an intramolecular F∙∙∙H hydrogen bond. However, 3-fluoropyrrolidine displayed extensive conformational diversity (ΔG0 among conformers ≤1.6 kcal⋅mol−1) as the intramolecular interactions were not sufficiently stabilizing to dictate a dominant

Synthesis of 4-(2-fluorophenyl)-7-methoxycoumarin: experimental and computational evidence for intramolecular and intermolecular C–F···H–C bonds

• Vuyisa Mzozoyana,
• Fanie R. van Heerden and
• Craig Grimmer

Beilstein J. Org. Chem. 2020, 16, 190–199, doi:10.3762/bjoc.16.22

• : DFT; F···H hydrogen bond; fluorinated phenylcoumarin; Pechmann reaction; through-space coupling; Introduction Coumarins constitute one of the big classes of naturally occurring compounds. The first coumarin was isolated from the tonka bean (Dipteryx odorata) in 1820 and, to date, more than 1300