96291-89-3Relevant academic research and scientific papers
Total Synthesis of (+)-Pipoxide and (+)-β-Senepoxide and Their Diene Precursors
Ogawa, Seiichiro,Takagaki, Tohei
, p. 2356 - 2359 (2007/10/02)
(2R)-trans-2,3-Diacetoxy-1-cyclohexa-4,6-diene (6), a diene precursor in the biosynthesis of highly oxygenated cyclohexane epoxides, has first been totally synthesized from the bromo lactone 16 derived from (1S)-endo-7-oxabicyclo2.2.1
SYNTHESIS AND EPOXIDATION OF TRANS-5,6-DIACETOXY-1-BENZOYLOXYMETHYL-1,3-CYCLOHEXADIENE.
Ogawa,Toyokuni,Ara,Suetsugu,Suami
, p. 1710 - 1714 (2007/10/02)
The title substituted 1,3-cyclohexadiene was prepared in three steps from the readily available DL-1,2-di-O-acetyl-(1,3/2)-3-bromomethyl-5-cyclohexene-1,2-diol. Epoxidation of it with m-chloroperoxybenzoic acid in 1,2-dichloroethane afforded several stere
SYNTHESIS AND EPOXIDATION OF TRANS-5,6-DIACETOXY-1-BENZOYLOXYMETHYL-1,3-CYCLOHEXADIENE
Ogawa, Seiichiro,Toyokuni, Tatsushi,Ara, Masayasu,Suetsugu, Masaru,Suami, Tetsuo
, p. 379 - 382 (2007/10/02)
Epoxidation of a newly prepared trans-5,6-diacetoxy-1-benzoyloxymethyl-1,3-cyclohexadiene by m-chloroperbenzoic acid in dichloroethane gave several isomeric compounds of the biologically important highly oxygenated cyclohexane derivatives.
