95475-65-3

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 7585-39-9 β‐cyclodextrin 
• 7585-39-9 β-cyclodextrin 

Downstream Products

• 98853-90-8 C₅₇H₈₅N₅O₃₆S₂ 
• 98126-99-9 6^I,6^IV-dideoxy-6^I,6^IV-diazido-β-cyclodextrin 
• 95475-66-4 C₅₄H₇₈O₃₃S₂ 
• 123834-11-7 6^A,6^B,6^D-tri(O-tosyl) β-cyclodextrin 
• 123809-99-4 6^A,6^C,6^D-tri(O-tosyl) β-cyclodextrin 
• 123782-06-9 6^A,6^B,6^C-tri(O-tosyl) β-cyclodextrin 
• 123810-00-4 6^A,6^C,6^E-tri(O-tosyl) β-cyclodextrin 
• 123810-01-5 6^A,6^B,6^E-tri-O-(p-tosyl)-β-cyclodextrin 

Relevant academic research and scientific papers

Homo- and hetero-difunctionalized β-cyclodextrins: Short direct synthesis in gram scale and analysis of regiochemistry

The regioselective difunctionalization of cyclodextrins (CDs) leading to derivatives amenable to further transformations is a daunting task due to challenging purification and unambiguous characterization of the obtained regioisomers with similar physico-

Novel fluorinated amphiphilic cyclodextrin derivatives: Synthesis of mono-, di- and heptakis-(6-deoxy-6-perfluoroalkylthio)-β-cyclodextrins

A new series of fluorinated amphiphilic β-cyclodextrin derivatives has been synthesized. The strategy is based on the modification of the C-6 position of the mono-6-deoxy-6A-para-tolylsulfonyl, di-6A, 6D-deoxy-6A, 6D-(para-tolylsulfonyl) and heptakis-(6-deoxy-6-iodo)-β-cyclodextrin precursors. The synthesis lead to mono-perfluoroalkylthio-, di-perfluoroalkylthio- and heptakis-perfluoroalkylthio-β-cyclodextrin in excellent yields (90-99%).

6A6B, 6A6C, AND 6A6D-DITOSYLATES OF β-CYCLODEXTRIN

Regio-isomers, 6A6B, 6A6C, and 6A6D-ditosylates of β-cyclodextrin prepared by the reaction of β-cyclodextrin with tosyl chloride easily and effetively separated through reversed phase column chromatography and assigned.