| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275352 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
The reaction of triiodoisocyanuric acid (prepared from I2 and trichloroisocyanuric acid in 90% yield) with alkenes in the presence of oxygenated nucleophilic solvents (alcohols, AcOH and H2O) led to the corresponding β-iodoethers, β-iodoacetates and iodohydrins, in 66-98% isolated yield. Enolethers reacted with triiodoisocyanuric acid in MeOH to produce dialkylacetals (70-83%).
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Rodrigo da S. Ribeiro, Pierre M. Esteves, Marcio C.S. de Mattos,