297687-34-4Relevant academic research and scientific papers
1,5-Anhydro-D-fructose as chiral building block: A novel approach to 1-deoxymannojirimycin
Maier, Peter,Andersen, Soren Moller,Lundt, Inge
, p. 827 - 830 (2007/10/03)
A novel six-step synthesis of 1-deoxymannojirimycin from 1,5-anhydro-D-fructose in 35% overall yield is reported. The key steps are nucleophilic piperidine ring formation and subsequent Lewis acid induced pyran ether cleavage. Georg Thieme Verlag Stuttgart.
1,5-Anhydro-D-fructose: Stereoselective conversions to 1,5- anhydroalditols and deoxy/amino substituted analogues
Andersen, Soren M.,Lundt, Inge,Marcussen, Jan
, p. 717 - 725 (2007/10/03)
1,5-Anhydro-D-fructose (1) has been converted into crystalline oximes. 1,5-Anhydroalditols and 2-amino-2-deoxy-1,5-anhydroalditols have been prepared by stereoselective reduction procedures from 1 and from the oximes, respectively.
