| Literature DB >> 35095338 |
Oleksandr S Olifir1,2, Anton V Chernykh1, Alexey V Dobrydnev1,2, Oleksandr O Grygorenko1,2, Yuriy S Moroz2,3, Zoia V Voitenko2, Dmytro S Radchenko1.
Abstract
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).Entities:
Keywords: building blocks; cyclization; organofluorine compounds; small rings; spiro compounds
Year: 2020 PMID: 35095338 PMCID: PMC8791643 DOI: 10.1002/ejoc.202000432
Source DB: PubMed Journal: European J Org Chem ISSN: 1099-0690