158634-64-1Relevant articles and documents
Synthesis of-lactams from acids and imines using thiocarbonyldiimidazole
Zarei, Maaroof,Karimi-Jaberi, Zahed,Movahedi, Amin
, p. 728 - 734 (2013/01/15)
Thiocarbonyldiimidazole has been found to be an efficient acid activator for the synthesis of-lactams by ketene-imine cycloaddition at room temperature. The experimental procedure is simple and results in excellent yields of the products. All products wer
Synthesis of structurally diverse 2-azetidinones via staudinger reaction on a solid support
Jarrahpour, Aliasghar,Fadavi, Abdolhamid,Zarei, Maaroof
experimental part, p. 320 - 327 (2011/05/14)
Trimellitic anhydride was attached to Merrifield resin and a ketene was generated from polymer-bound phthaloylglycine. Then this polymer reacted with imines in the presence of Vilsmeier reagent and triethylamine to afford the solid-phase-tethered β-lactam products. Selective cleavage of supported β-lactams by trifluoroacetic acid and methylhydrazine gave 4-carboxyphthalimido- and 3-amino-β-lactams, respectively. The trans-stereochemistry was found in all products.
The Vilsmeier reagent: a useful and versatile reagent for the synthesis of 2-azetidinones
Jarrahpour, Aliasghar,Zarei, Maaroof
experimental part, p. 2927 - 2934 (2009/05/30)
(Chloromethylene)dimethylammonium chloride (Vilsmeier reagent), prepared easily from N,N-dimethylformamide and oxalyl chloride or thionyl chloride, works as a versatile acid activator reagent for the direct [2+2] ketene-imine cycloaddition of substituted