New synthetic route to Pummerer's ketone

Article abstract of DOI:10.1080/00397919208020498

Pummerer's ketone 1 is obtained with an overall yield of 55% by the following sequence: Claisen rearrangement of an arylcyclohexylether 3; allylic oxidation of the methylcycloalkylphenolic derivative 4b, then spontaneous cyclisation during demethylation t

Full text of DOI:10.1080/00397919208020498

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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New Synthetic Route to
Pummerer's Ketone
J. M. Vierfond a , A. Reynet b , H. Moskowitz b & C.
Thal c
a Faculté de Pharmacie , 34 rue du Jardin des
Plantes, 86034, Poitiers, France
b Laboratoire de Chimie Organique , associé
au CNRS , Faculté de Pharmacie, 92290,
Ch[acaron]tenay-Malabry, France
c Institut de Chimie des Substances Naturelles,
CNRS , 91198, Gif-sur-Yvette, France
Published online: 23 Sep 2006.
To cite this article: J. M. Vierfond , A. Reynet , H. Moskowitz & C. Thal (1992) New
Synthetic Route to Pummerer's Ketone, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 22:12, 1783-1792,
DOI: 10.1080/00397919208020498
To link to this article: http://dx.doi.org/10.1080/00397919208020498
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