Mild, Efficient, One-Pot Synthesis of Imidazolones Promoted by N,O-Bistrimethylsilylacetamide (BSA) - Normandie Université Accéder directement au contenu
Article Dans Une Revue SYNLETT Année : 2016

Mild, Efficient, One-Pot Synthesis of Imidazolones Promoted by N,O-Bistrimethylsilylacetamide (BSA)

L. Colombeau
J. Hédouin
  • Fonction : Auteur

Résumé

The formation of imidazolones by means of dehydrative cyclization was developed, using bistrimethylsilylacetamide. This highly versatile, friendly, safe, and cost-effective reagent exhibited a very large scope of starting materials, since it can promote the formation of 4-benzylidene imidazolones, 4,4-dialkyl-imidazolones, bearing alkyl, aryl, or even no substituent at C2, the latter being unavailable by classical methods. This reagent also afforded clean and high-yielding one-pot reactions in the presence of amine or imine reagents.

Domaines

Chimie
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Dates et versions

hal-02046228 , version 1 (22-02-2019)

Identifiants

Citer

M. Muselli, L. Colombeau, J. Hédouin, Christophe Hoarau, Laurent Bischoff. Mild, Efficient, One-Pot Synthesis of Imidazolones Promoted by N,O-Bistrimethylsilylacetamide (BSA). SYNLETT, 2016, 27 (20), pp.2819-2825. ⟨10.1055/s-0035-1562524⟩. ⟨hal-02046228⟩
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