Studies on anhydro-osazones. Structure and anomeric configuration of the 3,6-anhydro-osazone derivatives obtained from D-galacto-2-heptulose phenylosazone

Dehydration of D-galacto-2-heptulose phenylosazone with methanolic sulfuric acid afforded two 3,6-anhydro-osazone derivatives (2 and 3). Compound 2 was obtained as the preponderant isomer, without inversion at C-1 (C-3 of the starting osazone), and 3 was obtained with inversion. The anomeric configurations of 2 and 3 were determined by n.m.r. spectroscopy. Refluxing of 2 and 3 with copper sulfate afforded two C-nucleoside analogs, namely, 4-β- and 4-α- D-lyxofuranosyl-2-phenyl-1,2,3-triazole, 4 and 5, respectively. The anomeric configurations of 4 and 5 were determined by n.m.r and c.d. spectroscopy. Acetylation of 4 and 5 afforded the tri-O-acetyl derivatives. The mass spectra of these compounds were discussed.     

Granulocytopoiesis in children with acute lymphoblastic leukaemia.

Numbers, proliferative potential, and differentiative capacity of bone marrow granulocyte-macrophage precursor cells were studied in 130 children with acute lymphoblastic leukaemia (ALL), including 77 children in an acute phase of the disease and 53 in remission. Bone marrow samples from 65 children without haematopoietic abnormalities were used as controls. The numbers of clonogenic precursors were found to be below normal in all phases of ALL, particularly during the acute period when the bone marrow was heavily infiltrated with leukaemic cells. It is shown that the decreases in the numbers and proliferative potential of the precursor cells during the acute phases was associated with the effects of leukaemic blast cells, but that in remission the observed reduction in the precursor cell pool was due to the cytostatic effect of therapy. The differentiative capacity of clonogenic granulocyte and macrophage precursors was not altered in children with ALL.