2009
DOI: 10.1016/j.tet.2009.08.053
|View full text |Cite
|
Sign up to set email alerts
|

Reactivity of 1,2-cyclic sulfite xylosides towards nucleophiles

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
2
0

Year Published

2010
2010
2022
2022

Publication Types

Select...
3
2
1

Relationship

1
5

Authors

Journals

citations
Cited by 6 publications
(2 citation statements)
references
References 21 publications
0
2
0
Order By: Relevance
“…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%