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B. M. Teresa, J. C. M. Adilia, C.D. Maycockd and T. Michaud, “Stereoselective Synthesis Of Optically Active Mono and Diaminoalcohols,” Tetrahedron, Vol. 61, No. 33, 2005, pp. 7960-7966. doi:10.1016/j.tet.2005.06.011

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.