Results 111 to 120 of about 669 (167)
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Orally active amino functionalized antimalarial 1,2,4-trioxanes

Bioorganic & Medicinal Chemistry Letters, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Chandan, Singh   +2 more
openaire   +2 more sources

A Vibrational Study of Some 1,2,4‐Trioxanes

Helvetica Chimica Acta, 1988
AbstractThe vibrational spectra of some 1,2,4‐trioxanes present two characteristic bands at 790 and 880 cm−1. On the basis of 18O‐isotopic substitution and comparison with analogous compounds, these bands have been assigned to coupled CO and OO stretching modes of the COO element.
Mohnhaupt, Martin Klaus   +6 more
openaire   +2 more sources

The Synthesis of 1,2,4‐Trioxan‐5‐ones

Helvetica Chimica Acta, 1991
AbstractSeveral 3,6‐substituted 1,2,4‐trioxan‐5‐ones have been prepared in good yield by condensing aldehydes and ketones with trimethylsilyl α‐[(trimethylsilyl)peroxy]alkanoates in the presence of trimethylsilyl trifluoromethane sulfonate as catalyst.
Jefford, Charles   +3 more
openaire   +2 more sources

Further explorations on bridged 1,2,4-trioxanes

Tetrahedron, 2007
Abstract Three new bicyclo[3.2.1]-type 1,2,4-trioxanes have been designed and synthesized. One of them demonstrates better tolerance of the intramolecular hemiketals to steric crowding in hydroperoxidation. The other represents a prototype for possible manipulation of the transient radicals generated in cleavage reactions.
Qi Zhang, Yikang Wu
openaire   +1 more source

A holegenocyclisation route to 1,2,4-trioxanes

Tetrahedron Letters, 1993
Hemiperoxyacetals derived from 2,3-dimethylbut-1-en-3-yl hydroperoxide and aliphatic aldehydes undergo cyclisation with NIS or NBS to afford the corresponding 3-alkyl-5-halogenomethyl-5,6,6-trimethyl-5,6,6-trimethyl-1,2,4-trioxanes in yields of 20–65%
A.J. Bloodworth, Aneela Shah
openaire   +1 more source

Synthesis and reaction of 1,2,4-trioxanes

Journal of the Chemical Society, Perkin Transactions 1, 1989
The peroxides (1a–e) and epoxides (2a–g) in methylene dichloride were treated with tungsten(VI) oxide and then with catalytic amounts of chlorosulphonic acid to give the corresponding 1,2,4-trioxanes (3a–r) in 10–63% yield. The mode of decomposition of the 1,2,4-trioxanes was studied by treating a number with the following reagents: triethylamine ...
Tomohiro Fujisaka   +3 more
openaire   +1 more source

ChemInform Abstract: SYNTHESIS OF 1,2,4‐TRIOXANES

Chemischer Informationsdienst, 1981
AbstractDas Peroxid (I) bildet in Gegenwart des Epoxids (II) das Trioxan (III).
M. MIURA, M. NOJIMA, S. KUSABAYASHI
openaire   +1 more source

Potent Antimalarial 1,2,4‐Trioxanes through Perhydrolysis of Epoxides

Chemistry – A European Journal, 2013
AbstractPerhydrolysis of a sterically congested multifunctional epoxide was achieved in ethereal H2O2 with the aid of a recently developed Mo catalyst. The resulting hydroperoxide cyclized to give a 1,2,4‐trioxane, which could be readily elaborated into qinghaosu and a range of novel analogues.
Hao, Hong-Dong   +2 more
openaire   +3 more sources

1,2,4-Trioxanes as Masked, Dual Purpose, Functional Groups

HETEROCYCLES, 1989
Scission reductrice de trioxannes-1,2,4 condenses en glycols et cetones ou aldehydes par Zn/acide ...
Jefford, Charles   +2 more
openaire   +2 more sources

ChemInform Abstract: cis‐Fused Dihydrofurano‐1,2,4‐trioxanes.

ChemInform, 1997
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
C. W. JEFFORD   +4 more
openaire   +1 more source

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