Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bettina V. Ernholt"'
Autor:
Bettina V. Ernholt, Anders Lohse, Rita G. Hazell, I. Thomsen, Xifu Liang, Mikael Bols, Astrid Jakobsen, Igor W. Plesner, Kenneth B. Jensen
Publikováno v:
Chemistry - A European Journal. 6:278-287
For the first time the two enantiomeric forms of the glycosidase inhibitor 1-azafagomine have been synthesised starting from D- and L-xylose. D-Xylose was converted to the 2,3,5-tribenzylfuranose, which upon reductive amination with tert-butyl carbaz
Publikováno v:
Synlett. 1999:701-704
Publikováno v:
Tetrahedron. 53:9357-9364
(±)-5-fluoro-4-hydroxy-3-hydroxymethylhexahydropyridazine (7) and some other azafagomine analogues were synthesis ed with the aim of comparing their glycosidase inhibition to that of (±)-4,5-dihydroxy-3-hydroxymethylhexahydropyridazine (1-azafagomi
Publikováno v:
ChemInform. 28
(±)-5-fluoro-4-hydroxy-3-hydroxymethylhexahydropyridazine (7) and some other azafagomine analogues were synthesis ed with the aim of comparing their glycosidase inhibition to that of (±)-4,5-dihydroxy-3-hydroxymethylhexahydropyridazine (1-azafagomi
Publikováno v:
ChemInform. 30
Autor:
Anders Lohse, Bettina V. Ernholt, Mikael Bols, Olle Matsson, Jadwiga Trocha-Grimshaw, Ole Hammerich, Inger Søtofte, Bengt Långström
Publikováno v:
Acta chemica Scandinavica (Copenhagen, Denmark : 1989). 52(4)
(6R)-6-(Hydroxymethyl)piperazin-2-one (1), (6S)-6-(hydroxymethyl)piperazin-2-one (2) and (6S)-6-[(1R, 2S, 3R)-1,2,3,4-tetrahydroxybutyl]piperazin-2-one (3) have been prepared in optically pure forms starting from D-glucosamine hydrochloride (4). The