An improved procedure for the synthesis of bicyclo[2.2.2]octane-2.6-dione

Article abstract of DOI:10.1080/00397919308011243

Conjugate addition of Meldrum's acid to 2-cyclohexenone followed by direct cyclization in PPA/acetic acid constitutes a shorter, more reproducible and higher yielding route to bicyclo[2.2.2]octane-2,6-dione than previous methods. The crude dione could be

Full text of DOI:10.1080/00397919308011243

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Synthetic Communications: An
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An Improved Procedure
for the Synthesis of
Bicyclo[2.2.2]octane-2,6-dione
Fredrik Almqvist a , Lars Eklund a & Torbjöm Frejd a
a Department of Organic Chemistry , Umeå
University , S-901 87, Umeå, Sweden
Published online: 23 Sep 2006.
To cite this article: Fredrik Almqvist , Lars Eklund & Torbjöm Frejd (1993) An
Improved Procedure for the Synthesis of Bicyclo[2.2.2]octane-2,6-dione, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:11, 1499-1505, DOI: 10.1080/00397919308011243
To link to this article: http://dx.doi.org/10.1080/00397919308011243
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