84543-36-2Relevant articles and documents
Synthesis of enantiomerically pure (2S)-2-endo-hydroxymethyl-5- norbornene by Diels-Alder reaction based on a new fructose-derived auxiliary
Nouguier,Mignon,Gras
, p. 1412 - 1414 (2007/10/03)
-
Preparation and catalytic hydrogenolysis of some ω-halogenoalkyl β-D-fructopyranosides; a convenient route to simple alkyl β-D-fructopyranosides
Raaijmakers, Harry W. C.,Eveleens, Susan M.,Arnouts, Esther G.,Zwanenburg, Binne,Chittenden, Gordon J. F.
, p. 511 - 514 (2007/10/02)
The acid-catalysed reactions of D-fructose, sucrose and inulin with ω-halogenoalkyl alcohols yield the corresponding β-D-fructopyranosides.Catalytic hydrogenolysis of these glycosides provides a simple route to some crystalline alkyl β-D-fructopyranosides of potential biological interest.
Chiral Syntheses of (R)-Spirobi-1,4-dioxan and Related Compounds from D-Fructose
Chan, Jonathan Y. C.,Hough, Leslie,Richardson, Anthony C.
, p. 1151 - 1153 (2007/10/02)
Syntheses of (R)-1,4,7,10-tetraoxaspiroundecane (spirobi-1,4-dioxan), (R)-1,4,7-trioxa-10-thiaspiroundecane, and (R)-1,4,7-trioxa-10-azaspiroundecane from 2'-chloroethyl β-D-fructopyranoside are reported, in which the chirality of the spiro-ring junction is defined by the configuration of the anomeric carbon atom of the glycoside.