E. Alonso, C. Del Pozo and J. Gonzalez, “Staudinger Reactions of Unsymmetrical Cyclic Ketenes: A Synthetically Useful Approach to Spiro β-Lactams and Derivatives. Reaction Mechanism and Theoretical Studies,” Journal of the Chemical Society, Perkin Transactions, Vol. 1, No. 4, 2002, pp. 571-576. doi:10.1039/b103279h

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.