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- W2024884790 endingPage "5606" @default.
- W2024884790 startingPage "5581" @default.
- W2024884790 abstract "Although the Burgess reagent (methoxycarbonylsulfamoyltriethylammonium hydroxide, inner salt) has found significant use in chemical synthesis as a dehydrating agent, almost no work has been directed towards its potential in other synthetic applications. As this article will detail, we have found that the Burgess reagent is remarkably effective at accomplishing a number of non-dehydrative synthetic tasks when applied to appropriate substrates, such as the formation of sulfamidates from 1,2-diols or epoxyalcohols, alpha- and beta-glycosylamines from carbohydrates, and cyclic sulfamides from 1,2-aminoalcohols. Beyond delineating the power of these new reaction manifolds, we also describe the construction of a group of alternative Burgess-type reagents that extends the scope of these new reactions even further." @default.
- W2024884790 created "2016-06-24" @default.
- W2024884790 creator A5049276572 @default.
- W2024884790 creator A5051119122 @default.
- W2024884790 creator A5065008454 @default.
- W2024884790 creator A5066329303 @default.
- W2024884790 creator A5085302439 @default.
- W2024884790 date "2004-11-19" @default.
- W2024884790 modified "2023-10-09" @default.
- W2024884790 title "New Uses for the Burgess Reagent in Chemical Synthesis: Methods for the Facile and Stereoselective Formation of Sulfamidates, Glycosylamines, and Sulfamides" @default.
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