Novel 2-aryl-3,4,5-trihydroxypiperidines: Synthesis and glycosidase inhibition

Samankaltaisia teoksia

• Synthesis and glycosidase inhibition of the enantiomer of (-)-steviamine, the first example of a new class of indolizidine alkaloid.
  Tekijä: Hu, X, et al.
  Julkaistu: (2010)
• Synthesis and glycosidase inhibition of broussonetine M and its analogues
  Tekijä: Wu, Q, et al.
  Julkaistu: (2019)
• Synthesis of three branched iminosugars [(3R,4R,5S)-3-(hydroxymethyl)piperidine-3,4,5-triol, (3R,4R,5R)-3-(hydroxymethyl)piperidine-3,4,5-triol and (3S,4R,5R)-3-(hydroxymethyl)piperidine-3.4,5-triol] and a branched trihydroxynipecotic acid [(3R,4R,5R)-3,4,5-trihydroxypiperidine-3-carboxylic acid] from sugar lactones with a carbon substituent at C-2
  Tekijä: Simone, M, et al.
  Julkaistu: (2012)
• Synthesis and Glycosidase Inhibition of Broussonetine M and Its Analogues
  Tekijä: Qing-Kun Wu, et al.
  Julkaistu: (2019-10-01)
• Isolation synthesis and glycosidase inhibition profile of 3-epi-casuarine
  Tekijä: Van Ameijde, J, et al.
  Julkaistu: (2006)