A convenient synthesis of 2,2-diphenyl-cyclohexanone and 6,6-diphenyl-2-cyclohexen-one

Article abstract of DOI:10.1080/00397919208019080

A short, convenient and large scale synthesis of 2,2-diphenyl-cyclohexanone and 6,6-diphenyl-2-cyclohexen-one using respectively the regioselective hydrogenolysis of 1,3-diketone (3) and the radical reduction of 3-bromo-2-enone (4) is reported.

Full text of DOI:10.1080/00397919208019080

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Convenient Synthesis of 2,2-
Diphenyl-Cyclohexanone and
6,6-Diphenyl-2-Cyclohexen-
One
Eric Bacqué a & Jean-Marc Paris a
a Centre de Recherche de Vitry-Alfortville, Rhône-
Poulenc Rorer , 13 Quai Jules Guesde BP, 14 94403,
Vitry sur Seine, Cedex, France
Published online: 24 Sep 2006.
To cite this article: Eric Bacqué & Jean-Marc Paris (1992) A Convenient Synthesis
of 2,2-Diphenyl-Cyclohexanone and 6,6-Diphenyl-2-Cyclohexen-One, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:15, 2259-2272, DOI: 10.1080/00397919208019080
To link to this article: http://dx.doi.org/10.1080/00397919208019080
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