Abstract
A reação de cicloadição [3+4] entre diferentes dienos (ciclopentadieno, 2-metilfurano e furano) e halocetonas levou aos cicloadutos correspondentes, cuja reação de ozonólise forneceu os ozonídeos 3a,5a-Dimetil-8,9,10-trioxatriciclo[5.2.1.12,6]undecan-4-ona (6), 2,3a,5a-Trimetil-8,9,10,11-tetraoxatriciclo[5.2.1.12,6]undecan-4-ona (9), 2,3b,5b-Trimetil-8,9,10,11-tetraoxatriciclo[5.2.1.12,6]undecan-4-ona (10, isômero exo), 2,3b,5b-Trimetil-8,9,10,11-tetraoxatriciclo [5.2.1.12,6]undecan-4-ona (11, isômero endo), 3a-Isopropil-8,9,10,11-tetraoxatriciclo[5.2.1.12,6]undecan-4-ona (14). A atividade antimalárica dos ozonídeos foi avaliada em testes "in vitro" contra cepas de Plasmodium falciparum, oriundos da Tailândia.
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