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Synlett 2011(1): 69-72
DOI: 10.1055/s-0030-1259082
DOI: 10.1055/s-0030-1259082
LETTER
© Georg Thieme Verlag
Stuttgart ˙ New York
Efficient Ring Opening of Protected and Unprotected Aziridines Promoted by Stable Zinc Selenolate in Ionic Liquid
Further Information
Received
1 October 2010
Publication Date:
07 December 2010 (online)
Publication History
Publication Date:
07 December 2010 (online)
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Abstract
A highly efficient protocol is reported for the synthesis of chiral β-seleno amines via the ring-opening reaction of aziridines. Under neutral conditions, employing a stable phenyl selenolate specie (PhSeZnBr) and (BMIM)BF4 as solvent, β-seleno amines were obtained in good to excellent yields. Reuse of the ionic liquid was also possible, and four runs were performed with no decrease in the yields.
Key words
chiral β-seleno amines - ring opening reaction - aziridine - ionic liquid
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- Supporting Information
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References and Notes
Detailed procedure in the Supporting Information.