Mild and Efficient Synthesis of B-Amino Alcohols by Bismuthtrichloride Catalysed Opening of Epoxides
A. Thirupathaiah1*, S. Ramanna2 and G. Venkateswar Rao2
1Department of Chemistry, Satavahana University, Karimnagar - 505 001 (India).
2Department of Chemistry, Kakatiya University, Warangal - 506 009 (India).
Nucleophilic opening of epoxides with aniline derivatives in the presence of catalytic amount of bismuthtrichloride in acetonitrile at room temperature afforded the corresponding b-amino alcohols in excellent to very good yield.
KEYWORDS:Epoxide; bismuthtrichloride; nucleophilic opening; aromatic amine; b-aminoalcohols
Download this article as:Copy the following to cite this article: Thirupathaiah A, Ramanna S, Rao G. V. Mild and Efficient Synthesis of B-Amino Alcohols by Bismuthtrichloride Catalysed Opening of Epoxides. Orient J Chem 2009;25(1). |
Copy the following to cite this URL: Thirupathaiah A, Ramanna S, Rao G. V. Mild and Efficient Synthesis of B-Amino Alcohols by Bismuthtrichloride Catalysed Opening of Epoxides. Orient J Chem 2009;25(1). Available from: http://www.orientjchem.org/?p=23367 |
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