927809-65-2Relevant academic research and scientific papers
Synthesis of a poly-hydroxypyrolidine-based inhibitor of Mycobacterium tuberculosis GlgE
Veleti, Sri Kumar,Lindenberger, Jared J.,Thanna, Sandeep,Ronning, Donald R.,Sucheck, Steven J.
, p. 9444 - 9450 (2014)
(Chemical Equation Presented). Long treatment times, poor drug compliance, and natural selection during treatment of Mycobacterium tuberculosis (Mtb) have given rise to extensively drug-resistant tuberculosis (XDR-TB). As a result, there is a need to iden
Polyhydroxylated pyrrolidines: synthesis from d-fructose of new tri-orthogonally protected 2,5-dideoxy-2,5-iminohexitols
Izquierdo, Isidoro,Plaza, María T.,Yá?ez, Victor
, p. 1440 - 1447 (2007/10/03)
The readily available 3-O-benzyl-1,2-O-isopropylidene-β-d-fructopyranose (2) was transformed into its 5-O- (3) and 4-O-benzoyl (4) derivative. Compound 4 was straightforwardly transformed into 5-azido-4-O-benzoyl-3-O-benzyl-5-deoxy-1,2-O-isopropylidene-β-
