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| SHORTPAPER | Synthesis 2007: 666-668 DOI: 10.1055/s-2007-965921 |
© Georg Thieme Verlag Stuttgart · New York
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Catalyst-Free Highly Regio- and Stereoselective Ring Opening of Epoxides and Aziridines with Sodium Azide Using Poly(ethylene glycol) as an Efficient Reaction Medium
[1]
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| Biswanath Das*, Vtukuri Saidi Reddy, Fouzia Tehseen, Maddeboina Krishnaiah |
Organic Chemistry Division - I, Indian Institute of Chemical Technology, Hyderabad 500 007, India Fax: +91(40)7160512; e-Mail: biswanathdas@yahoo.com;
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Received
10 November 2006 |
Abstract
Ring opening of epoxides and aziridines has readily been carried out at room temperature using poly(ethylene glycol) (PEG-400) as the efficient reaction medium to form the corresponding 2-azido alcohols and 2-azido amines, respectively, in excellent yields (95-99%) within 30-45 minutes and with high regio- and streoselectivity. Key words
epoxide - aziridine - PEG-400 - 2-azido alcohol - 2-azido amine
1 Part 103 in the series ‘Studies on Novel Synthetic Methodologies'; IICT Communication no. 061206.
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