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G. Attolino, G. Catelani and F. D’Andrea, “Regiospecific Synthesis of 4-Deoxy-d-threo-Hex-3-enopyranosides by Simultaneous Activation–Elimination of the Talopyranoside Axial 4-OH with the NaH/Im2SO2 System: Manifestation of the Stereoelectronic Effect,” European Journal of Organic Chemistry, Vol. 2006, No. 23, pp. 5279-5292. http://dx.doi.org/10.1002/ejoc.200600526

has been cited by the following article:

• TITLE: Improvement on the Synthesis of Primary Amino Sugar Derivatives via N-Benzyl Intermediates

  AUTHORS: Massimo Corsi, Marco Bonanni, Giorgio Catelani, Felicia D’Andrea, Tiziana Gragnani, Roberto Bianchini

  KEYWORDS: Amino Sugars; Nucleophilic Substitution; Benzylamine; Primary Tosylates

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.3 No.3A, November 6, 2013

  ABSTRACT: Primary tosylates 1a-d were converted to the corresponding amino species 3a-d. Benzylamine was proved effective for the substitution of tosylates, using acetonitrile (MeCN) as the solvent of choice and citric acid to remove excess of the reagent from crude products 2a-d. Debenzylation was carried out at circa (ca.) atmospheric pressure of hydrogen gas in the presence of acetic acid (AcOH). The method was also demonstrated in a demo batch experiment for the synthesis of compound 3a on a 50 g scale of 1a.