2009
DOI: 10.1016/j.tet.2009.08.053
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Reactivity of 1,2-cyclic sulfite xylosides towards nucleophiles

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Cited by 6 publications
(2 citation statements)
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References 21 publications
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“…Following our success in stabilising thionyl-and sulfuryl-chlorides in ILs thus enabling formation of sulfite and sulfate derivatives of carbohydrates with much improved yields. 14,15 We report here the use of ILs to modulate chlorination versus sulfonation of a range of diols. 2 H NMR was used to monitor the reactions and demonstrates how the chemoselectivity and product distribution can be controlled by using IL solvents.…”
Section: Introductionmentioning
confidence: 99%
“…Following our success in stabilising thionyl-and sulfuryl-chlorides in ILs thus enabling formation of sulfite and sulfate derivatives of carbohydrates with much improved yields. 14,15 We report here the use of ILs to modulate chlorination versus sulfonation of a range of diols. 2 H NMR was used to monitor the reactions and demonstrates how the chemoselectivity and product distribution can be controlled by using IL solvents.…”
Section: Introductionmentioning
confidence: 99%
“…As a consequence, in ILs cyclic sulfites and sulfates could find a wider range of applications in organic synthesis and large scale productions, in particular in C-nucleoside chemistry. 4…”
mentioning
confidence: 99%