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Novel Nucleophilic Trifluoromethylation of Vicinal Diol Cyclic Sulfates
A novel method for highly regioselective and stereospecific nucleophilic trifluoromethylation of vicinal diol cyclic sulfates, using the reagent derived from reduction of trifluoromethyl iodide by tetrakis(dimethylamino)ethylene (TDAE), is presented.
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Published in: | Organic letters 2002-12, Vol.4 (26), p.4671-4672 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
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cites | cdi_FETCH-LOGICAL-a311t-983006c0df21cc20f384664dd2fd7dd0a9dd1c17a4d6e32bd5304d1632d3268e3 |
container_end_page | 4672 |
container_issue | 26 |
container_start_page | 4671 |
container_title | Organic letters |
container_volume | 4 |
creator | Takechi, Naoto Ait-Mohand, Samia Medebielle, Maurice Dolbier, William R |
description | A novel method for highly regioselective and stereospecific nucleophilic trifluoromethylation of vicinal diol cyclic sulfates, using the reagent derived from reduction of trifluoromethyl iodide by tetrakis(dimethylamino)ethylene (TDAE), is presented. |
doi_str_mv | 10.1021/ol0270374 |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Novel Nucleophilic Trifluoromethylation of Vicinal Diol Cyclic Sulfates |
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