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M. Chini, P. Crotti, L. Favero, F. Machhia and M. Pine-schi, “Lanthanide(III) Trifluoromethanesulfonates as Ex- Traordinarily Effective New Catalysts for the Aminolysis of 1,2-Epoxides,” Tetrahedron Letters, Vol. 35, No. 3, 1994, pp. 433-436. doi:10.1016/0040-4039(94)85073-9

has been cited by the following article:

• TITLE: Highly Regio-Selective Synthesis of β-Amino Alcohol by Reaction with Aniline and Propylene Carbonate in Self Solvent System over Large Pore Zeolite Catalyst

  AUTHORS: Anil K. Kinage, Pravin P. Upare, Anandkumar B. Shivarkar, Sunil P. Gupte

  KEYWORDS: β-Amino Alcohol, Proplylene Carbonate, Zeolite, Catalyst, Chemo-Selectivity

  JOURNAL NAME: Green and Sustainable Chemistry, Vol.1 No.3, August 31, 2011

  ABSTRACT: The nucleophilic ring opening of epoxides with amines is a well known route for the synthesis of β-amino alcohols. The use of carbonates offers significant advantages over epoxides as they are far less hazardous materials, safe for handling, do not require high-pressure equipment and most notably the possibility of solvent less reactions. In this work, utilization of zeolite as host catalyst in the reaction media for synthesis of β-amino alcohols without using solvent is reported.