1H and 13C NMR spectra and solution structures of novel derivatives of 5-substituted creatinines

Author(s):  
Hanna Krawczyk ◽  
Agnieszka Pietras ◽  
Anna Kraska
1995 ◽  
Vol 60 (2) ◽  
pp. 311-323 ◽  
Author(s):  
Miloš Buděšínský ◽  
Miloslav Černý ◽  
Ivan Černý ◽  
Stanislav Sámek ◽  
Tomáš Trnka

The corresponding acetylated and free 2-O- and 4-O-glucosyl derivatives of dianhydrohexoses Ib - VIIb and Ic - VIIc have been obtained by the reactions of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide (IX) with 1,6:3,4- and 1,6:2,3-dianhydro-β-D-hexopyranoses (Ia - VIIa). Structure of the products and the effects of glycosylation upon chemical shifts and conformations of the disaccharides prepared have been studied using 1H and 13C NMR spectra.


1990 ◽  
Vol 55 (10) ◽  
pp. 2493-2501 ◽  
Author(s):  
Karel Dlabal ◽  
Karel Palát ◽  
Antonín Lyčka ◽  
Želmíra Odlerová

Homolytic amidations of 2-chloropyrazine and 6-chloropyrazine-2-carbonitrile have been carried out to obtain products which have been used to prepare sulfur derivatives of pyrazine as potential tuberculostatic agents. The 1H and 13C NMR spectra of the products have been measured and interpreted, and the antituberculotic activity has been evaluated.


ChemInform ◽  
2010 ◽  
Vol 29 (3) ◽  
pp. no-no
Author(s):  
J. W. TIMMERMANS ◽  
P. M. P. BOGAERT ◽  
D. DE WIT ◽  
J. F. G. VLIEGENTHART

2018 ◽  
Vol 69 (1) ◽  
pp. 64-69
Author(s):  
Liviu Birzan ◽  
Mihaela Cristea ◽  
Constantin C. Draghici ◽  
Alexandru C. Razus

The 1H and 13C NMR spectra of several 2,6-diheteroarylvinyl heterocycles containing 4-azulenyl moiety were recorded and their proton and carbon chemical shifts were compared with those of the compounds without double bond between the heterocycles. The influence of the nature of central and side heterocycles, molecule polarization and anisotropic effects were revealed. The highest chemical shifts were recorded for the pyrylium salts and the lowest at pyridines, but in the case of the pyridinium salts, the protons chemical shifts at the central heterocycle are more shielded due to a peculiar anisotropy of the attached vinyl groups.


1994 ◽  
Vol 262 (2) ◽  
pp. 173-184 ◽  
Author(s):  
Tadasu Urashima ◽  
William A. Bubb ◽  
Michael Messer ◽  
Yuhnagi Tsuji ◽  
Yasuko Taneda

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