Determination of the absolute chirality of tellurium using resonant diffraction with circularly polarized x-rays

2010 ◽  
Vol 22 (12) ◽  
pp. 122201 ◽  
Author(s):  
Y Tanaka ◽  
S P Collins ◽  
S W Lovesey ◽  
M Matsumami ◽  
T Moriwaki ◽  
...  
2012 ◽  
Vol 24 (15) ◽  
pp. 159501 ◽  
Author(s):  
Y Tanaka ◽  
S P Collins ◽  
S W Lovesey ◽  
M Matsunami ◽  
T Moriwaki ◽  
...  

2010 ◽  
Vol 81 (14) ◽  
Author(s):  
Yoshikazu Tanaka ◽  
Taro Kojima ◽  
Yasutaka Takata ◽  
Ashish Chainani ◽  
Stephen W. Lovesey ◽  
...  

2004 ◽  
Vol 43 (21) ◽  
pp. 2853-2856 ◽  
Author(s):  
Roman Fasel ◽  
Joachim Wider ◽  
Christoph Quitmann ◽  
Karl-Heinz Ernst ◽  
Thomas Greber

1992 ◽  
Vol 70 (10) ◽  
pp. 2664-2676 ◽  
Author(s):  
Wayne B. Severn ◽  
James C. Richards

The specific capsular polysaccharide produced by Rhodococcusequi serotype 3 was found to be a high-molecular-weight acidic polymer composed of D-glucose, D-galactose, D-glucuronic acid, 4-O-[(S)-1-carboxyethyl]-D-mannose, and pyruvic acid in equal molar proportions. Structural analysis, employing a combination of chemical and nuclear magnetic resonance techniques, established that the polysaccharide is composed of linear repeating tetrasaccharide units,[Formula: see text]in which (R)-1-carboxyethylidene groups bridge the O-2 and O-3 positions of the β-D-glucuronic acid residues. The 1H and 13C NMR resonances of the native and depyruvulated serotype 3 polysaccharides were fully assigned by homo- and heteronuclear chemical shift correlation methods. The absolute configurations of the lactate-substituted mannopyranosyl residues and the pyruvate acetals were determined from 1H–1H NOE measurements on the intact polysaccharide. Unequivocal determination of the absolute chirality of the 4-O-[(S)-1-carboxyethyl]-β-D-mannopyranose residues was achieved by 1H–1H NOE measurements on an acetylated lactone derivative of the glycose.


2011 ◽  
Vol 84 (21) ◽  
Author(s):  
Yoshikazu Tanaka ◽  
Taro Kojima ◽  
Yasutaka Takata ◽  
Ashish Chainani ◽  
Stephen W. Lovesey ◽  
...  

The importance of absolute, as opposed to relative, intensity measurements in X-ray crystal analysis has often been stressed, and such measurements may lead, with compounds where one sort of atom is of dominant importance, to a direct and unequivocal determination of the structure. Their value in the analysis of organic compounds, where usually no atoms are predominant in X-ray scattering power, is perhaps not so immediate; nevertheless, the absolute X-ray reflection of a given substance is at least as important a constant as, say, its thermal conductivity, and its determination is a necessary preliminary to any detailed study by the X-ray method. Hitherto such absolute measurements have been confined to inorganic substances e. g. , rock-salt, usually occurring in large crystals. It seemed to be worth while to make a determination of the absolute reflecting power of a typical organic crystal in conditions similar to those employed in the analysis of such crystals, i. e. , using a small crystal completely bathed in a monochromatic pencil of X-rays. A very suitable substance for such a measurement is anthracene , since it is easily obtained pure and in crystals which are reasonably permanent and simple to adjust, but more particularly because its structure is already known in considerable detain and relative intensity measurements described in this paper will enable workers with other crystals to standardize series of relative intensity measurements with the minimum of labour, by comparing directly one of their observed reflections with the (001) reflection from a small weighed crystal of anthracene. The comparison can be made without difficulty, either photographically using an integrating microphotometer or by the ionization method on an ordinary spectrometer.


Nature ◽  
1951 ◽  
Vol 168 (4268) ◽  
pp. 271-272 ◽  
Author(s):  
J. M. BIJVOET ◽  
A. F. PEERDEMAN ◽  
A. J. van BOMMEL

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