Furanose Bicyclophosphites as Synthons of Modified Nucleoside Diphosphates

Abstract

Previously we synthesized and examined in detail 1,2- alkylideneglucofuanose 3,5,6-bicyclophosphites; mono- and bicyclophosphates with peculiar chemical and physiological activity were obtained on their base [1]. During the study of their structural dependence, we modified the hydrocarbonic moiety, synthesiz-ed 1,2,3- and 3,5,6-bicyclophosphites and cyclophosphates of gulofuanose, and correlated their features with those of glucose analogues. Furthermore, an additional phosphonate moiety (obtained by a stereoselective reaction of an appropriate ketonic sugar with silylphosphites) was introduced into the glucofuranose 3,5,6-bicyclophosphite molecule to the third carbon atom. As a result, the monosaccharide matrix gained two functional groups containing tri- and fourcoordinated phosphorus.     

One-dimensional coherent four-wave mixing as a way to image the spatial distribution of atoms in a laser-produced plasma

An experimental technique based on coherent one-dimensional hyper-Raman-resonant four-wave mixing in broad cylindrically focused light beams has been developed for line-by-line imaging of spatial distribution of excited atoms in a low-temperature plasma of optical breakdown. The technique was applied to map excited lead atoms in a low-temperature laser-produced plasma.     

Reactivity of the Hydroxy Groups in Melezitose and Their Selective Protection

The reactivity of melezitose hydroxy groups was studied by tritylation in pyridine with subsequent acetylation. After partial detritylation of the products, acetyl group transfer from position 4 to 6 was observed. The structure of the prepared melezitose derivatives was established on the basis of their IR, ¹H, ¹³C, and ¹H-¹H COSY NMR, and mass spectra (fast atom bombardment), as well as from the results of model calculations performed with the aid of SGI Indigo Molecule-Pattern-Work-Station software package (Biosym) where the potential energy function was approximated with the CVFF potential. The reactivity of primary hydroxy groups in melezitose was found to decrease in the following order: 6' > 6 6' > 1'.     

Synthesis and structure of 1,2-O-isopropylidene-α-D-glucofuranose 3,5-phenylcyclophosphonate

L. Ya. Karpov Scientific-Research Physical Chemistry Institute. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 3, pp. 67–73, May–June, 1991.     

Binuclear heterometallic {M-Ln} pivalate complexes (M = Co, Ni, Cu; Ln = Sm, Gd): synthesis, structure, and thermolysis

Binuclear heterometallic complexes (??²-bpy)CoLn(Piv)₅(H₂O), (??²-bpy)NiLn(Piv)₅(H₂O), and (??²-bpy)CuLn(Piv)₅(HPiv) (Ln = Sm or Gd, Piv- is the pivalate anion) were synthesized. A comparative study of the structural characteristics and the thermolysis of the resulting compounds was performed.