Results 101 to 110 of about 669 (167)
Phosphite ozonides as singlet oxygen sources for organic synthesis and the preparation of novel endoperoxide-containing antimalarials [PDF]
Rawe, Sarah-Louise
core +1 more source
Contemporary approaches to malaria chemotherapy : novel quinoline and peroxide-based antimalarial frugs [PDF]
Mukhtar, Amira
core +1 more source
An evaluation of the cytotoxicity of the dihydroartemisinin-acridine hybrids and tetra-oxane dimmers against leukaemia and colon cancer cells lines ‘1’ [PDF]
Rinki, Rinki
core
Some of the next articles are maybe not open access.
Related searches:
Related searches:
New orally active spiro 1,2,4-trioxanes with high antimalarial potency
Bioorganic and Medicinal Chemistry Letters, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
Chandan, Singh +2 more
exaly +3 more sources
Piperidine dispiro-1,2,4-trioxane analogues
Bioorganic & Medicinal Chemistry Letters, 2008Dispiro N-Boc-protected 1,2,4-trioxane 2 was synthesised via Mo(acac)(2) catalysed perhydrolysis of N-Boc spirooxirane followed by condensation of the resulting beta-hydroperoxy alcohol 10 with 2-adamantanone. N-Boc 1,2,4-trioxane 2 was converted to the amine 1,2,4-trioxane hydrochloride salt 3 which was subsequently used to prepare derivatives (4-7 ...
Sunil, Sabbani +6 more
openaire +3 more sources
Tetrahedron Letters, 1994
Abstract Allylic hydroperoxides CH 2 :C(Ph)CH(OOH)CH 2 OX (X H, CONHPh, Ac), from regiospecific photooxygenation of allylic alcohols CH 3 C(Ph):CHCH 2 OX, form hemiperoxyacetals with aldehydes or ketones which upon cyclisation with mercury(II) trifluoroacetate then reduction with sodium borohydride diastereoselectively afford 1,2,4-trioxanes with ...
A.J. Bloodworth, Karen A. Johnson
+4 more sources
Abstract Allylic hydroperoxides CH 2 :C(Ph)CH(OOH)CH 2 OX (X H, CONHPh, Ac), from regiospecific photooxygenation of allylic alcohols CH 3 C(Ph):CHCH 2 OX, form hemiperoxyacetals with aldehydes or ketones which upon cyclisation with mercury(II) trifluoroacetate then reduction with sodium borohydride diastereoselectively afford 1,2,4-trioxanes with ...
A.J. Bloodworth, Karen A. Johnson
+4 more sources
Journal of the Chemical Society, Chemical Communications, 1981
The reaction of a mixture of α-hydroxydecyl hydroperoxide [or bis(α-hydroxyalkyl) peroxides] and epoxides in the presence of tungstic anhydride and catalytic amounts ofchlorosulphonic acid gave the corresponding 1,2,4-trioxans in 7–63% yield.
Masahiro Miura +2 more
openaire +1 more source
The reaction of a mixture of α-hydroxydecyl hydroperoxide [or bis(α-hydroxyalkyl) peroxides] and epoxides in the presence of tungstic anhydride and catalytic amounts ofchlorosulphonic acid gave the corresponding 1,2,4-trioxans in 7–63% yield.
Masahiro Miura +2 more
openaire +1 more source
1,2,4-Trioxanes as potential antimalarial agents
Journal of Medicinal Chemistry, 1988A number of 1,2,4-trioxanes were prepared and tested for antimalarial activity in search of a simplified analogue of the naturally occurring antimalarial qinghaosu. The compounds were assayed in an in vitro system for antimalarial activity against chloroquine-susceptible and chloroquine-resistant strains of Plasmodium falciparum.
J A, Kepler +4 more
openaire +2 more sources

