Аннотация:
Novel fluorinated α-epoxycyclohexanes were synthesized in up to 96% yields by epoxidation of the Diels–Alder adducts of β-fluoro-β-nitrostyrenes and 2,3-dimethylbuta-1,3-diene. The epoxidation with m-chloroperoxybenzoic acid and subsequent hydrolysis into diols were found to proceed in a highly stereoselective manner.
Образец цитирования:
V. E. Shambalova, R. V. Larkovich, S. A. Ponomarev, A. S. Aldoshin, K. A. Lyssenko, V. G. Nenajdenko, “Stereoselective epoxidation of 4-fluoro-4-nitrocyclohexenes”, Mendeleev Commun., 33:4 (2023), 463–465