Antimalarial endoperoxides that are potent and easily synthesized

[1] Anders M.W., 1985, BIOACTIVATION FOREIG, P121

[2] Structure-activity relationships of the antimalarial agent artemisinin .3. Total synthesis of (+)-13-carbaartemisinin and related tetra- and tricyclic structures [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (09) : 1885 - 1897

[3] CUMMING JN, 1996, ADV PHARMACOL, V37, P253

[4] THE TOXICITY OF ARTEMISININ AND RELATED-COMPOUNDS ON NEURONAL AND GLIAL-CELLS IN CULTURE [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 1995, 96 (03) : 263 - 271

[5] GOLDSMITH RS, 1992, BASIC CLIN PHARM, P735

[6] Artemisinin and the antimalarial endoperoxides: From herbal remedy to targeted chemotherapy [J]. MICROBIOLOGICAL REVIEWS, 1996, 60 (02) : 301 - +

[7] OU-YANG K, 1990, Antimicrobial Agents and Chemotherapy, V34, P1961

[8] THE CHEMOTHERAPY OF RODENT MALARIA .50. THE ACTIVITIES OF SOME SYNTHETIC 1,2,4-TRIOXANES AGAINST CHLOROQUINE-SENSITIVE AND CHLOROQUINE-RESISTANT PARASITES .3. OBSERVATIONS ON FENOZAN-50F, A DIFLUORINATED 3,3'-SPIROCYCLOPENTANE 1,2,4-TRIOXANE [J]. ANNALS OF TROPICAL MEDICINE AND PARASITOLOGY, 1993, 87 (02): : 111 - 123

[9] Mechanism-based design of simple, symmetrical, easily prepared, potent antimalarial endoperoxides [J]. TETRAHEDRON LETTERS, 1996, 37 (06) : 815 - 818

[10] EVIDENCE FOR FE(IV)=O IN THE MOLECULAR MECHANISM OF ACTION OF THE TRIOXANE ANTIMALARIAL ARTEMISININ [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (21) : 5885 - 5886

[1] Anders M.W., 1985, BIOACTIVATION FOREIG, P121

[2] Structure-activity relationships of the antimalarial agent artemisinin .3. Total synthesis of (+)-13-carbaartemisinin and related tetra- and tricyclic structures [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (09) : 1885 - 1897

[3] CUMMING JN, 1996, ADV PHARMACOL, V37, P253

[4] THE TOXICITY OF ARTEMISININ AND RELATED-COMPOUNDS ON NEURONAL AND GLIAL-CELLS IN CULTURE [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 1995, 96 (03) : 263 - 271

[5] GOLDSMITH RS, 1992, BASIC CLIN PHARM, P735

[6] Artemisinin and the antimalarial endoperoxides: From herbal remedy to targeted chemotherapy [J]. MICROBIOLOGICAL REVIEWS, 1996, 60 (02) : 301 - +

[7] OU-YANG K, 1990, Antimicrobial Agents and Chemotherapy, V34, P1961

[8] THE CHEMOTHERAPY OF RODENT MALARIA .50. THE ACTIVITIES OF SOME SYNTHETIC 1,2,4-TRIOXANES AGAINST CHLOROQUINE-SENSITIVE AND CHLOROQUINE-RESISTANT PARASITES .3. OBSERVATIONS ON FENOZAN-50F, A DIFLUORINATED 3,3'-SPIROCYCLOPENTANE 1,2,4-TRIOXANE [J]. ANNALS OF TROPICAL MEDICINE AND PARASITOLOGY, 1993, 87 (02): : 111 - 123

[9] Mechanism-based design of simple, symmetrical, easily prepared, potent antimalarial endoperoxides [J]. TETRAHEDRON LETTERS, 1996, 37 (06) : 815 - 818

[10] EVIDENCE FOR FE(IV)=O IN THE MOLECULAR MECHANISM OF ACTION OF THE TRIOXANE ANTIMALARIAL ARTEMISININ [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (21) : 5885 - 5886