Keywords
1,2-dienes
1Z,5Z-1,5-dienes
cytotoxicity
homo-cyclomagnesiation
macrodiolides
substituted tetrahydrofurans
Abstract
A novel strategy for synthesizing new polyfunctional macrodiolides based on the oxidative cyclization of (1Z,5Z)-diene bonds to form 2,5-disubstituted tetrahydrofurans has been developed. The unsaturated macrodiolide was obtained using an original catalytic homo-cyclomagnesiation of O-containing 1,2-dienes (the Dzhemilev reaction). The macrocyclic compounds demonstrated cytotoxic activity in tests on Jurkat, A549, and HEK293 cell lines.
Funders
Ministry of Education and Science of the Russian Federation
FMRS-2025-0047
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