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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 15, 1985 - Issue 11
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Original Articles

An Improved Synthesis of Deslongchamps's Diketone by Direct Regioselective Functionalization of endo-Dicyclopentadiene

Elena Carceller Departament de Química Orgànica. Facultat de Química, Universitat de Barcelona, E-08028, Barcelona, Spain
,
M. Lluïsa García Departament de Química Orgànica. Facultat de Química, Universitat de Barcelona, E-08028, Barcelona, Spain
,
Albert Moyano Departament de Química Orgànica. Facultat de Química, Universitat de Barcelona, E-08028, Barcelona, Spain
&
Fèlix Serratosa Departament de Química Orgànica. Facultat de Química, Universitat de Barcelona, E-08028, Barcelona, Spain
Pages 951-958 | Published online: 19 Dec 2006
 
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Abstract

A high yield three-step synthesis of endo-tricyclo[5.2.1.02,6]deca-4,8-dione (Deslongchamps's diketone) by a stepwise regioselective oxymercuration of commercial endo-dicyclopentadiene is described.

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