Ramirez, M.A., Ortiz, G., Levin, G., McCormack, W., Blanco, M.M., Perillo, I.A. and Salerno, A. (2014) Rapid and Efficient Synthesis of Five- to Eight-Membered Cyclic Aminals under Ultrasound Irradiation. Tetrahedron Letters, 55, 4774-4776.
https://doi.org/10.1016/j.tetlet.2014.06.061

has been cited by the following article:

• TITLE: Ultrasound Promoted Synthesis and Antimicrobial Evaluation of Novel Seven and Eight-Membered 1,3-Disubstituted Cyclic Amidinium Salts

  AUTHORS: María M. Blanco, María A. Reamírez, María C. Caterina, Isabel A. Perillo, Guido A. Oppezzo, María S. Shmidt, Gabriel O. Gutkind, José Di Conza, Alejandra Salerno

  KEYWORDS: Medium Ring Amidinium Salts, Ultrasonic Assisted Synthesis, Antimicrobial, Green Chemistry

  JOURNAL NAME: Open Journal of Medicinal Chemistry, Vol.10 No.4, December 28, 2020

  ABSTRACT: Series of 1,3-dibenzyl-1H-4,5,6,7-tetrahydro-1,3-diazepinium and 1,4,5,6,7,8-hexahydro-1,3-diazocinium salts derivatives were efficiently synthesized in excellent yields by dehydrogenation of the corresponding N,N'-dibenzyl aminals employing N-bromosuccinimide (NBS) as dehydrogenating agent under ultrasound irradiation. The present methodology has proven to be simple, efficient and environmentally benign. All novel compounds were identified and characterized by 1H and 13C NMR spectra. The synthesized compounds were screened for their antimicrobial activities.