PREPARATION, THIN LAYER CHROMATOGRAPHY, AND ULTRAVIOLET SPECTRA OF SOME O-BENZYL DERIVATIVES OF D-GLUCOSE

1963 ◽  
Vol 41 (7) ◽  
pp. 1801-1806 ◽  
Author(s):  
M. E. Tate ◽  
C. T. Bishop

A new method for benzylation of carbohydrates has been developed which facilitated complete substitution of hydroxyl groups in one of the compounds prepared. Thin layer chromatography provides a good criterion of purity and is also a preparative method for separation of identifiable amounts of O-benzyl derivatives of carbohydrates. The number of benzyl groups in a compound can be determined by ultraviolet absorption spectroscopy. The following compounds were prepared, some of which have not been reported previously: benzyl-2,3,4,6-tetra-O-benzyl-α-D-glucoside; benzyl 2,3,4,6-tetra-O-benzyl-β-D-glucoside; methyl 2,3,4,6-tetra-O-benzyl-α-D-glucoside; 2,3,4,6-tetra-O-benzyl-α-D-glucose; l-O-(p-nitro-benzoyl)-2,3,4,6-tetra-O-benzyl-α-D-glucose; octa-O-benzyl sucrose; 3,5-di-O-benzyl-1,2-O-cyclohexylidene-α-D-xylose.

1966 ◽  
Vol 49 (4) ◽  
pp. 774-778
Author(s):  
Fred E Hearth ◽  
Daniel E Ott ◽  
Francis A Gunther

Abstract A new method combining oscillopolarography and thin layer chromatography is described for the microdetermination of residual Morestan in Valencia orange rind; 0.5 ppm is readily detectable, but accurate quantitation is difficult below 1.0 ppm. Data obtained by this method are comparable to those from a colorimetric method.


Screening ◽  
1995 ◽  
Vol 4 (1) ◽  
pp. 17-26 ◽  
Author(s):  
H. Ohtake ◽  
Y. Hase ◽  
K. Sakemoto ◽  
T. Oura ◽  
Y. Wada ◽  
...  

1967 ◽  
Vol 102 (3) ◽  
pp. 815-824 ◽  
Author(s):  
J. C. Fletcher

1. A system of separation using buffered Celite columns is described that enables the pipsyl derivatives of most of the common amino acids to be separated. 2. The reaction of pipsyl chloride with several amino acids not included in previous studies has been investigated. In particular, knowledge of the acid-soluble pipsyl derivatives of arginine, histidine, lysine, tyrosine and cysteic acid has been extended. 3. Reproducible factors have been obtained that enable corrections to be applied for the breakdown of pipsylamino acids on acid hydrolysis. 4. The reaction of pipsyl chloride with peptides has been studied under various conditions. 5. The extent of the reaction between pipsyl chloride and insulin depends on the nature of the solvent-buffer system, and under the best conditions so far found is about 75% complete. 6. In an Appendix, the separation of pipsylamino acids by thin-layer chromatography is described.


Sign in / Sign up

Export Citation Format

Share Document