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A. D. Borthwick, G. Weingarte, T. M. Haley, M. Tomaszewski, W. Wang, Z. Hu, J. Bedard, H. Jin, L. Yuen and T. S. Mansour, “Design and Synthesis of Monocyclic β-Lactams as Mechanismbased Inhibitors of Human Cytomegalovirus Protease,” Bioorganic & Medicinal Chemistry Letters, Vol. 8, No. 4, 1998, pp. 365-370. doi:10.1016/S0960-894X(98)00032-8

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.