Synthesis of new 4-methyl-3-piperidones via an iron-catalyzed intramolecular tandem isomerization-aldolisation process - Université de Rennes Accéder directement au contenu
Article Dans Une Revue Tetrahedron Année : 2012

Synthesis of new 4-methyl-3-piperidones via an iron-catalyzed intramolecular tandem isomerization-aldolisation process

Résumé

A new versatile synthesis of 3-piperidones is described, starting from amino acids. It uses, as a key step, an iron carbonyl-mediated intramolecular tandem isomerization-aldolisation reaction. These new heterocycles appear as useful scaffolds for the total synthesis of various types of bioactive molecules.

Domaines

Chimie organique

Dates et versions

hal-00842352 , version 1 (08-07-2013)

Identifiants

Citer

Dinh Hung Mac, Abdul Sattar, Srivari Chandrasekhar, Jhillu Singh Yadav, René Grée. Synthesis of new 4-methyl-3-piperidones via an iron-catalyzed intramolecular tandem isomerization-aldolisation process. Tetrahedron, 2012, 68 (43), pp.8863-8868. ⟨10.1016/j.tet.2012.08.048⟩. ⟨hal-00842352⟩
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