ChemInform Abstract: SYNTHESIS OF D-GLUCURONIC ACID DERIVATIVES OF 5-FLUOROURACIL HAVING O-GLYCOSIDIC LINKAGE

1978 ◽  
Vol 9 (2) ◽  
Author(s):  
M. KANEKO ◽  
H. TANAKA ◽  
M. KIMURA ◽  
B. SHIMIZU
1977 ◽  
Vol 25 (9) ◽  
pp. 2458-2460 ◽  
Author(s):  
MASAKATSU KANEKO ◽  
HIROYUKI TANAKA ◽  
MISAKO KIMURA ◽  
BUNJI SHIMIZU

1933 ◽  
Vol 100 (3) ◽  
pp. 743-748 ◽  
Author(s):  
Walther F. Goebel ◽  
Frank H. Babers

1938 ◽  
Vol 124 (1) ◽  
pp. 207-220
Author(s):  
Walther F. Goebel ◽  
Richard E. Reeves

Molecules ◽  
2000 ◽  
Vol 5 (12) ◽  
pp. 600-601
Author(s):  
Mariano Castro ◽  
Natalia Salmaso ◽  
José Kovensky ◽  
Alicia Cirelli

2003 ◽  
Vol 81 (5) ◽  
pp. 364-375 ◽  
Author(s):  
Jonathan Watts ◽  
Jesús Jiménez-Barbero ◽  
Ana Poveda ◽  
T Bruce Grindley

The conformations of a series of derivatives of the disaccharide α-L-fucopyranosyl-(1[Formula: see text]3)-2-acetamido-2-deoxy-D-glucopyranoside, part of the Lex determinant, were studied by molecular modelling using the MM3* forcefield and by 1H NMR spectroscopy. Unusually shielded O-benzyl protons were observed in the 1H NMR spectrum of phenyl 2,3,4-tri-O-benzyl-α-L-fucopyranosyl-(1[Formula: see text]3)-2-deoxy-2-phthalimido-1-thio-α-D-glucopyranoside and assigned to the 2-O-benzyl group. This observation was explained by a shift in the population of the conformational mixture present about the glycosidic linkage from the positive Ψ region in the unsubstituted disaccharide to the negative Ψ region induced by π-stacking between the phthalimide and the 2-O-benzyl phenyl ring. The experimental nuclear Overhauser enhancements confirm the accuracy of the calculations.Key words: disaccharide, conformation, π-stacking, Lex determinant, NOE measurements, MM3 calculations.


1967 ◽  
Vol 105 (3) ◽  
pp. 1269-1274 ◽  
Author(s):  
M M Abou-el-Makarem ◽  
P Millburn ◽  
R L Smith ◽  
R T Williams

1. The extent of the excretion in the bile of the rat of benzene and 21 of its simple derivatives was studied. 2. Some 16 compounds of molecular weight less than 200, and including neutral molecules (benzene and toluene), aromatic acids, aromatic amines and phenols, were injected in solution intraperitoneally into biliary-cannulated rats. Metabolites in the bile were identified and estimated. The extent of biliary excretion of these compounds was low, i.e. 0–10% of the dose in 24hr., and most appeared in the bile mainly as conjugates. 3. The biliary excretion of six conjugates of molecular weight less than 300, including three glycine conjugates, one sulphate conjugate, one glucuronic acid conjugate and two acetyl derivatives, was low (less than 3% of the dose). 4. It is concluded that simple benzene derivatives of molecular weight less than about 300 are poorly excreted in rat bile.


1962 ◽  
Vol 82 (4) ◽  
pp. 578-583 ◽  
Author(s):  
Yoshihiro Nitta ◽  
Junji Ide ◽  
Atsushi Momose ◽  
Yasuo Nakajima

2000 ◽  
Vol 131 (11) ◽  
pp. 1197-1205 ◽  
Author(s):  
Monika Poláková ◽  
Dušan Joniak ◽  
Miloslav Ďuriš

1933 ◽  
Vol 100 (2) ◽  
pp. 573-581
Author(s):  
Walther F. Goebel ◽  
Frank H. Babers

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