13143-95-8Relevant academic research and scientific papers
Investigations into the decomposition of aminoacyl-substituted monosaccharide scaffolds from a drug discovery library
He,Wimmer,Verquin,Meutermans,Ferro
, p. 4070 - 4079 (2015/03/30)
This study investigated the unexpected decomposition and associated intermediates of compound 1, a specific member of a drug discovery library based on a monosaccharide scaffold. LC/MS and NMR spectroscopic analyses indicated that, under acidic conditions
Efficient synthesis of 4-amino-4-deoxy-L-arabinose and spacer-equipped 4-amino-4-deoxy-L-arabinopyranosides by transglycosylation reactions
Mueller, Bernhard,Blaukopf, Markus,Hofinger, Andreas,Zamyatina, Alla,Brade, Helmut,Kosma, Paul
experimental part, p. 3143 - 3151 (2010/10/21)
Methyl 4-azido-4-deoxy-l-arabinopyranoside has been synthesized in five steps starting from methyl-d-xylopyranoside in a multigram scale without chromatographic purification in 78% overall yield. The transformation relied on selective tosylation/nosylatio
IDENTIFICATION OF THE 2-HYDROXYMETHYL-3,4-DIHYDROXYPYRROLIDINE (OR 1,4-DIDEOXY-1,4-IMINOPENTITOL) FROM ANGYLOCALYX BOUTIQUEANUS AND FROM ARACHNIODES STANDISHII AS THE (2R, 3R, 4S)-ISOMER BY THE SYNTHESIS OF ITS ENANTIOMER.
Jones, D. Wyn C.,Nash, Robert J.,Bell, E. Arthur,Williams, J. Michael
, p. 3125 - 3126 (2007/10/02)
The D-xylo and L-arabino isomers of 1,4-dideoxy-1,4-iminopentitol have been synthesised from L-arabinose, and the L-arabino isomer was found to be the enantiomer of the alkaloid from Angylocalyx Boutiqueanus.The alkaloid from Arachniodes Standishii, recently reported to have the xylo configuration, was also shown to be the D-arabino isomer.
