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Practical Synthesis of Aryl Triflates under Aqueous Conditions
A practical and efficient synthesis of aryl triflates under biphasic basic aqueous conditions is described. The current methodology provides entry into these valuable substrates that omits the use of amine bases and allows facile isolation by simple solvent evaporation after phase separation. Good y...
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Published in: | Organic letters 2002-12, Vol.4 (26), p.4717-4718 |
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Main Authors: | , , , , |
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Language: | English |
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cites | cdi_FETCH-LOGICAL-a309t-90270a5999e0df97cba4d6234af79c8061f996e20c87e09dacb4537b963fada93 |
container_end_page | 4718 |
container_issue | 26 |
container_start_page | 4717 |
container_title | Organic letters |
container_volume | 4 |
creator | Frantz, Doug E Weaver, Damian G Carey, James P Kress, Michael H Dolling, Ulf H |
description | A practical and efficient synthesis of aryl triflates under biphasic basic aqueous conditions is described. The current methodology provides entry into these valuable substrates that omits the use of amine bases and allows facile isolation by simple solvent evaporation after phase separation. Good yields can also be obtained without the use of organic solvent. |
doi_str_mv | 10.1021/ol027154z |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Practical Synthesis of Aryl Triflates under Aqueous Conditions |
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