Iron(II)-mediated rearrangement of 1,2,4-trioxanes into 1,2-diol monoesters via 1,5-hydrogen transfer
- 9 October 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (41) , 7551-7554
- https://doi.org/10.1016/0040-4039(95)01530-2
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Replacement of the nonperoxidic trioxane oxygen atom of artemisinin by carbon: Total synthesis of (+)-13-carbaartemisinin and related structuresTetrahedron Letters, 1995
- Synthesis, Structure, and Antimalarial Activity of Some Enantiomerically Pure, cis‐fused cyclopenteno‐1,2,4‐trioxanesHelvetica Chimica Acta, 1995
- Evidence for Fe(IV):O in the Molecular Mechanism of Action of the Trioxane Antimalarial ArtemisininJournal of the American Chemical Society, 1995
- The Decomposition of cis‐Fused Cyclopenteno‐1,2,4‐Trioxanes induced by Ferrous Salts and some oxophilic reagentsHelvetica Chimica Acta, 1995
- Mechanism-Based Design, Synthesis, and in vitro Antimalarial Testing of New 4-Methylated Trioxanes Structurally Related to Artemisinin: The Importance of a Carbon-Centered Radical for Antimalarial ActivityJournal of Medicinal Chemistry, 1994
- Regiospecifically oxygen-18 labeled 1,2,4-trioxane: a simple chemical model system to probe the mechanism(s) for the antimalarial activity of artemisinin (qinghaosu).Journal of the American Chemical Society, 1992
- Synthesis of 1,2,4-trioxanes via intramolecular oxymercuriationJournal of the Chemical Society, Chemical Communications, 1991
- Synthesis of a prostaglandin endoperoxide model compound and its reaction with electron transfer reagentsTetrahedron, 1988
- Chemistry of 1,2,4-trioxanes. Formation of 1,2-diol monoestersJournal of the Chemical Society, Chemical Communications, 1985