327172-69-0Relevant academic research and scientific papers
Catalytic, stereoselective glycosylation - spiroketalization of 3,4,5-tri-o-benzyl-β-d-fructopyranose generating di-d-fructo-pyranose-1,2′:2,1′-dianhydride
Kaji, Eisuke,Saiga, Reiko,Kurimoto, Emiko,Nishino, Takashi
, p. 385 - 393 (2008/02/13)
α-D-Fructopyranose β-D-fructopyranose-1,2′:2,1′- dianhydride has been stereoselectively synthesized by tandem catalytic glycosylation-spiroketalization of 3,4,5-tri-O-benzyl-β-D-fructo- pyranose. Of the several protic acid catalysts which exist
Carbohydrate-derived spiroketals. Stereoselective synthesis of Di-d-fructose dianhydrides by boron trifluoride promoted glycosylation-spiroketalization of acetal precursors
Benito, Juan M.,Gomez-Garcia, Marta,Ortiz Mellet, Carmen,Garcia Fernandez, Jose M.,Defaye, Jacques
, p. 549 - 552 (2007/10/03)
(Matrix presented) Di-D-fructose 1,2′:2,1′-dianhydrides, dispiro-tricyclic disaccharides widely found in food materials, have been stereoselectively prepared in one-pot reaction from O-protected D-fructose 1,2-acetonide precursors by treatment with boron
