1,2,5,10,11,14-hexaoxadispiro[5.2.5.2]hexadecanes: Novel Spirofused Bis-trioxane Peroxides

Overview

Journal Molecules

Publisher MDPI

Specialty Biology

Date 2008 Sep 17

PMID 18794783

Citations 4

Authors

Axel G Griesbeck

Lars-Oliver Hoinck

Johann Lex

Jorg Neudorfl

Dirk Blunk

Tamer T El-Idreesy

Affiliations

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Abstract

A set of new bis-spirofused 1,2,4-trioxanes 4a-d was obtained from the reaction of cyclohexane-1,4-dione with allylic hydroperoxides 2a-d, bearing an additional hydroxy group in the homoallylic position, by diastereoselective photooxygenation of allylic alcohols 1a-d and subsequent BF(3)-catalyzed peroxyacetalization with the diketone. From the reaction of a monoprotected cyclohexane-1,4-dione 5 with the allylic hydroperoxide 6 derived from the singlet oxygenation of methyl hydroxytiglate, one monospiro compound was obtained, the 1,2,4-trioxane ketone 7, as well as a mixture of the diastereoisomeric syn- and anti bis-1,2,4-trioxanes 8. The structures of bis-1,2,4-trioxanes were examined theoretically by DFT methods and compared with X-ray structural data in order to evaluate the preferential trioxane ring conformational orientation.

Citing Articles

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Synthesis of spiroannulated and 3-arylated 1,2,4-trioxanes from mesitylol and methyl 4-hydroxytiglate by photooxygenation and peroxyacetalization.

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