Title of article :
Regioselective Ring Opening of Oxiranes to Halohydrins with Tetrabutylammonium Halide in Water in the Presence of -Cyclodextrin†
Author/Authors :
Surendra, K. Indian Institute of Chemical Technology - Organic Chemistry Division, India , Krishnaveni, N. Srilakshmi Indian Institute of Chemical Technology - Organic Chemistry Division, India , Kumar, V. Pavan Indian Institute of Chemical Technology - Organic Chemistry Division, India , Nageswar, Y.V.D. Indian Institute of Chemical Technology - Organic Chemistry Division, India , Rao, K. Rama Indian Institute of Chemical Technology - Organic Chemistry Division, India
From page :
652
To page :
658
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 b-cyclodextrin in aqueous medium.
Keywords :
Oxiranes , halohydrins , tetrabutylammonium halides , beta , cyclodextrin , water.
Journal title :
letters in organic chemistry
Journal title :
letters in organic chemistry
Record number :
2717909
Link To Document :
https://search.isc.ac/dl/search/defaultta.aspx?DTC=10&DC=2717909
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