Article citationsMore>>

B. Alcaide, P. Almendros, T. M. Del Campo, R. Rodríguez-Acebes, “Diversity-Oriented Preparation of Enantiopure Spirocyclic 2-Azetidinones from α-Oxo-β-Lactams through Barbier-Type Reactions Followed by Metal-Catalyzed Cyclizations,” Advanced Synthesis & Catalysis, Vol. 349, No. 4-5, 2007, pp. 749-758. doi:10.1002/adsc.200600502

has been cited by the following article:

• TITLE: Synthesis of Some New Spiro β-Lactams and Thiazolidinones Compounds Containing Sulfur Incorporating Quinon Compounds

  AUTHORS: Nadia Ali Ahmed Elkanzi

  KEYWORDS: β-Lactam; Spiro Thiazolidinone; Synthesized; Cycloaddition

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.2 No.4, December 27, 2012

  ABSTRACT: A series of spiro, β-Lactams, and thiazolidinones incorporating compounds 4 have been synthesized by cycloaddition reaction of, chloroacetyl chloride and mercaptoacetic acid with the synthesized Shiff,s bases 5a-c to give new spiro β- Lactam 6a-c and spiro thiazolidinone 7a-c the cycloaddition were characterized by spectral data including HNMR, 13C-NMR, IR and elemental analysis.