Isolation and structural analyses of positional isomers of 61,6m-di-O-α-d-mannopyranosyl-cyclomaltooctaose (m=2–5) and 6-O-α-(n-O-α-d-mannopyranosyl)-α-d-mannopyranosyl-cyclomaltooctaose (n=2, 3, 4, and 6)

This publication has 8 references indexed in Scilit:

• Isolation by HPLC of the positional isomers of 61,2n-di-O-α-d-galactopyranosylcyclomaltohexaose (n = 1–6) and determination of their structures by enzymatic degradation
  Carbohydrate Research, 1997
• Enzymatic Synthesis of Mannosyl-cyclodextrin by α-Mannosidase from Jack Bean
  Bioscience, Biotechnology, and Biochemistry, 1997
• Isolation by HPLC of the positional isomers of heterogeneous doubly branched cyclomaltohexaose having one α-d-galactosyl and one α-d-glucosyl side chain and determination of their structures by enzymatic degradation
  Carbohydrate Research, 1996
• Isolation and characterization of novel heterogeneous branched cyclomalto-oligosaccharides (cyclodextrins) produced by transgalactosylation with α-galactosidase from coffee bean
  Carbohydrate Research, 1995
• Separation and characterization of five positional isomers of trimaltosyl-cyclomaltoheptaose (trimaltosyl-β-cyclodextrin)
  Carbohydrate Research, 1994
• Preparation, isolation, and characterization of novel heterogeneous branched cyclomalto-oligosaccharides having β-d-galactosyl residue(s) on the side chain
  Carbohydrate Research, 1993
• Assignment of proton-decoupled carbon-13 spectra of complex molecules by using polarization transfer spectroscopy. A superior method to off-resonance decoupling
  Journal of the American Chemical Society, 1980
• 13C nuclear magnetic resonance spectra of glucobioses, glucotrioses, and glucans
  Journal of the Chemical Society, Perkin Transactions 1, 1973