Synthesis of structurally diverse 2-azetidinones via Staudinger reaction on a solid support

A Jarrahpour, A Fadavi, M Zarei

Index: Jarrahpour, Aliasghar; Fadavi, Abdolhamid; Zarei, Maaroof Bulletin of the Chemical Society of Japan, 2011 , vol. 84, # 3 p. 320 - 327

Full Text: HTML

Citation Number: 25

Abstract

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 ...