Eur. J. Org. Chem. 2021, 2021 (47), 6541-6550
DOI: 10.1002/ejoc.202000432
Olifir O.; Chernykh A.; Dobrydnev A.; Grygorenko O.; Moroz Y.; Voitenko Z.; Radchenko D.
A convenient methodology for constructing 6,6‐difluorospiro[3.3]heptane scaffold – a conformationally restricted isostere of gem ‐difluorocycloalkanes – is developed. Alarge array of novel 2‐mono‐ and 2,2‐bifunctionalized difluorospiro[3.3]heptane building blocks was obtained through the convergent synthesis strategy using a common synthetic precursor – 1,1‐bis(bromomethyl)‐3,3‐difluorocyclobutane. The target compounds and intermediates were prepared by short reaction sequences (6–10 steps) on multigram scale (up to 0.47 kg).