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Triptycene cyclopentenedione

Triptycene cyclopentenedione 47 underwent 1,3-DC with nitrile oxides affording polycyclic isoxazolines 48 bearing the triptycene moiety. The adducts 48 exist in solution in their two enolic forms 49 and 50, in equimolecular amounts <02JOC4612>. [Pg.265]

Spyroudis S, Xanthopoulou N. Triptycene quinones in synthesis preparation of triptycene cyclopentenedione and its reactivity as a dienophile. J. Org. Chem. 2002 67 4612-4614. [Pg.519]


See also in sourсe #XX -- [ Pg.265 ]




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