引用本文:
Jun XUE. Synthesis of D-Fructofuranosides Using Phenyl Thioglycosides as Glycosyl Donors[J]. Chinese Chemical Letters,
1997, 8(12): 1029-1030.
Citation: Jun XUE. Synthesis of D-Fructofuranosides Using Phenyl Thioglycosides as Glycosyl Donors[J]. Chinese Chemical Letters, 1997, 8(12): 1029-1030.
Citation: Jun XUE. Synthesis of D-Fructofuranosides Using Phenyl Thioglycosides as Glycosyl Donors[J]. Chinese Chemical Letters, 1997, 8(12): 1029-1030.
Synthesis of D-Fructofuranosides Using Phenyl Thioglycosides as Glycosyl Donors
摘要:
Benzoylated phenyl α-and β-2-thio-D-fructofuranosides were synthesized and firstly used as donors in coupling with sucrose acceptor.α-Fructofuranoside was stereospecifically synthesized by employing NIS (N-iodosuccinimide)/AgOTf as catalysts.The structure of all products was confirmed by 13C-NMR or 1H-NMR spectrum.
English
Synthesis of D-Fructofuranosides Using Phenyl Thioglycosides as Glycosyl Donors
Abstract:
Benzoylated phenyl α-and β-2-thio-D-fructofuranosides were synthesized and firstly used as donors in coupling with sucrose acceptor.α-Fructofuranoside was stereospecifically synthesized by employing NIS (N-iodosuccinimide)/AgOTf as catalysts.The structure of all products was confirmed by 13C-NMR or 1H-NMR spectrum.
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