Abstract
A novel reagent tetrabutylammonium halide has been utilized for the highly regioselective ring opening of oxiranes to halohydrins at room temperature in good yields involving β-cyclodextrin in aqueous medium.
Keywords: oxiranes, halohydrins, tetrabutylammonium halides, cyclodextrin, water
Letters in Organic Chemistry
Title: Regioselective Ring Opening of Oxiranes to Halohydrins with Tetrabutylammonium Halide in Water in the Presence of β-Cyclodextrin
Volume: 2 Issue: 7
Author(s): K. Surendra, N. S. Krishnaveni, V. P. Kumar, Y. V.D. Nageswar and K. R. Rao
Affiliation:
Keywords: oxiranes, halohydrins, tetrabutylammonium halides, cyclodextrin, water
Abstract: A novel reagent tetrabutylammonium halide has been utilized for the highly regioselective ring opening of oxiranes to halohydrins at room temperature in good yields involving β-cyclodextrin in aqueous medium.
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Cite this article as:
Surendra K., Krishnaveni S. N., Kumar P. V., Nageswar V.D. Y. and Rao R. K., Regioselective Ring Opening of Oxiranes to Halohydrins with Tetrabutylammonium Halide in Water in the Presence of β-Cyclodextrin, Letters in Organic Chemistry 2005; 2 (7) . https://dx.doi.org/10.2174/157017805774296821
DOI https://dx.doi.org/10.2174/157017805774296821 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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