An Improved Procedure for the Synthesis of Bicyclo[2.2.2]octane- 2,6-dione
Författare
Summary, in English
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 used as substrate for the baker's yeast reduction to (IR, 4S, 6S)-bicyclo[2.2.2]octane-6-ol-2-one.
Avdelning/ar
Publiceringsår
1993
Språk
Engelska
Sidor
1499-1505
Publikation/Tidskrift/Serie
Synthetic Communications
Volym
23
Issue
11
Dokumenttyp
Artikel i tidskrift
Förlag
Marcel Dekker
Ämne
- Organic Chemistry
Status
Published
ISBN/ISSN/Övrigt
- ISSN: 0039-7911