Regioselective Ring Opening of Oxiranes to Halohydrins with Tetrabutylammonium Halide in Water in the Presence of β-Cyclodextrin

K. Surendra; N. S. Krishnaveni; V. P. Kumar; Y. V.D. Nageswar; K. R. Rao

doi:10.2174/157017805774296821

ISSN: 1570-1786
E-ISSN: 1875-6255

Regioselective Ring Opening of Oxiranes to Halohydrins with Tetrabutylammonium Halide in Water in the Presence of β-Cyclodextrin
Authors: K. Surendra¹, N. S. Krishnaveni², V. P. Kumar³, Y. V.D. Nageswar⁴ and K. R. Rao⁵
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¹ Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India. ² Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India. ³ Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India. ⁴ Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India. ⁵ Organic Chemistry Division-I, Indian Institute of Chemical Technology, Hyderabad-500 007, India.
Source: Letters in Organic Chemistry, Volume 2, Issue 7, Nov 2005, p. 652 - 658
DOI: https://doi.org/10.2174/157017805774296821
- Available online: 01 Nov 2005

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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2005-11-01

2025-10-27

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Article Type: Review Article

Keyword(s): cyclodextrin; halohydrins; oxiranes; tetrabutylammonium halides; water

Regioselective Ring Opening of Oxiranes to Halohydrins with Tetrabutylammonium Halide in Water in the Presence of β-Cyclodextrin

Abstract

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