S. Sagava, H. Abe, Y. Hase and T. Inaba, “Catalytic Asymmetric Aminolysis of 3,5,8-Trioxabicyclo[5.1.0] Octane Providing an Optically Pure 2-Amino-1,3,4-buta- netriol Equivalent,” The Journal of Organic Chemistry, Vol. 64, No. 13, 1999, pp. 4962-4965. doi:10.1021/jo9900883

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.