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C. Palomo, J. M. Aizpurua, I. Ganboa and M. Oiarbide, “Asymmetric Synthesis of β-Lactams through the Staudinger Reaction and Their Use as Building Blocks of Natural and Nonnatural Products,” Current Medicinal Chemistry, Vol. 11, No. 14, 2004, pp. 1837-1872. doi:10.2174/0929867043364900

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.