28034-58-4

Upstream product

• 388-37-4 Trifluoro-acetic acid 2-methoxy-3,5-bis-(2,2,2-trifluoro-acetoxy)-6-(2,2,2-trifluoro-acetoxymethyl)-tetrahydro-pyran-4-yl ester 

Downstream Products

• 388-37-4 Trifluoro-acetic acid (2R,3R,4S,5S,6R)-2-methoxy-3,5-bis-(2,2,2-trifluoro-acetoxy)-6-(2,2,2-trifluoro-acetoxymethyl)-tetrahydro-pyran-4-yl ester 
• 388-37-4 Trifluoro-acetic acid (2S,3S,4R,5R,6S)-2-methoxy-3,5-bis-(2,2,2-trifluoro-acetoxy)-6-(2,2,2-trifluoro-acetoxymethyl)-tetrahydro-pyran-4-yl ester 
• 388-37-4 Trifluoro-acetic acid (2R,3S,4R,5R,6S)-2-methoxy-3,5-bis-(2,2,2-trifluoro-acetoxy)-6-(2,2,2-trifluoro-acetoxymethyl)-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

IMPROVED GAS CHROMATOGRAPHIC SEPARATION OF ENANTIOMERIC CARBOHYDRATE DERIVATIVES USING A NEW CHIRAL STATIONARY PHASE

Pentylated cyclomaltohexaose ( α-cyclodextrin ) can be used as a chiral stationary phase for cappilary g.l.c. in the range 40 deg to > 200 deg.Strong enantioselective molecular interactions are observed towards trifluoroacetylated carbohydrates, methyl glycosides, 1,4- and 1,5-anhydroalditols, polyols, and polyhydroxy acid methyl esters.Base-line resolution of enantiomers is achieved after only a few minutes.