724705-45-7Relevant academic research and scientific papers
Synthesis of 1,2-cis -homoiminosugars derived from GlcNAc and GaLNAc exploiting a β-amino alcohol skeletal rearrangement
Blriot, Yves,Auberger, Nicolas,Jagadeesh, Yerri,Gauthier, Charles,Prencipe, Giuseppe,Tran, Anh Tuan,Marrot, Jrme,Dsir, Jrme,Yamamoto, Arisa,Kato, Atsushi,Sollogoub, Matthieu
, p. 5512 - 5515 (2014)
The synthesis of 1,2-cis-homoiminosugars bearing an NHAc group at the C-2 position is described. The key step to prepare these α-d-GlcNAc and α-d-GalNAc mimics utilizes a β-amino alcohol skeletal rearrangement applied to an azepane precursor. This strateg
The first synthesis of substituted azepanes mimicking monosaccharides: A new class of potent glycosidase inhibitors
Li, Hongqing,Bleriot, Yves,Chantereau, Caroline,Mallet, Jean-Maurice,Sollogoub, Matthieu,Zhang, Yongmin,Rodriguez-Garcia, Eliazar,Vogel, Pierre,Jimenez-Barbero, Jesus,Sinay, Pierre
, p. 1492 - 1499 (2007/10/03)
The synthesis of the first examples of seven-membered ring iminoalditols, molecules displaying an extra hydroxymethyl substituent on their seven-membered ring compared to the previously reported polyhydroxylated azepanes, has been achieved from D-arabinos
