Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Anne Marie Horneman"'
Publikováno v:
Bioorganic & Medicinal Chemistry. 8:2803-2812
The synthesis of a series of 2-aryl substituted hetero annulated 1,3-oxazin-4-ones and their evaluation as specific inhibitors of the tissue factor (TF)/factor VIIa (FVIIa)-induced pathway of coagulation is reported. Inhibitory activities (IC50 value
Autor:
Inge Lundt, Anne Marie Horneman
Publikováno v:
Synthesis. 1999:317-325
Autor:
Anne Marie Horneman, Inge Lundt
Publikováno v:
The Journal of Organic Chemistry. 63:1919-1928
A novel type of carbasugars, carbaaldohexofuranoses, has been prepared using a 5-exo-trig radical cyclization of C-2 substituted 2,3-unsaturated 7-bromoheptono-1,4-lactones as the key step. During the cyclization step, two stereogenic centers were fo
Autor:
Inge Lundt, Anne Marie Horneman
Publikováno v:
Tetrahedron. 53:6879-6892
Three carbasugars: 5-Deoxycarba-α-L-xylo-hexofuranose, 5-deoxycarba-α-L-lyxo-hexofuranose and 5-deoxycarba-β-D-lyxo-hexofuranose have been prepared starting from readily available 2,7-dibromo-2,7-dideoxy-D-glycero-D-ido-heptono-1,4-lactone and 2,7
Autor:
Anne Marie Horneman, Inge Lundt
Publikováno v:
Journal of Carbohydrate Chemistry. 14:1-8
6-Bromo-6-deoxy-α-d-glucopyranosyl fluoride (2) was prepared in good yield from α-d-glucopyranosyl fluoride (1) by treatment with PPh3 and CBr4 in pyridine. Catalytic reduction of 2 gave the corresponding 6-deoxy-α-d-glucopyranosyl fluoride (3) wh
Autor:
Inge Lundt, Anne Marie Horneman
Publikováno v:
ChemInform. 26
6-Bromo-6-deoxy-α-d-glucopyranosyl fluoride (2) was prepared in good yield from α-d-glucopyranosyl fluoride (1) by treatment with PPh3 and CBr4 in pyridine. Catalytic reduction of 2 gave the corresponding 6-deoxy-α-d-glucopyranosyl fluoride (3) wh
Autor:
Inge Lundt, Anne Marie Horneman
Publikováno v:
ChemInform. 30
Publikováno v:
Synlett. 1995:918-920