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Synthesis 2007(3): 348-350
DOI: 10.1055/s-2007-965885
DOI: 10.1055/s-2007-965885
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York
Facile One-Step Synthesis of Mono-2-(p-Tolylsulfonyl)-β-cyclodextrin under Aqueous Conditions
Further Information
Received
21 September 2006
Publication Date:
12 January 2007 (online)
Publication History
Publication Date:
12 January 2007 (online)
Abstract
A new and convenient method is presented for the synthesis of mono-2-(p-tolylsulfonyl)-β-cyclodextrin under aqueous conditions that does not require large amounts of polar organic solvents such as DMF, metal-containing reagents such as dibutyltin oxide, or flammable bases such as NaH. Yields are typically around 20%.
Key words
cyclodextrins - sulfonates - regioselectivity - host-guest systems
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References
The response factor of the RI detector for both compounds was determined independently and is close to 1.