A facile synthesis and carbon-13 nuclear magnetic resonance spectral properties of 7-ketocholesteryl benzoate

Lipids ◽  
1987 ◽  
Vol 22 (10) ◽  
pp. 760-763 ◽  
Author(s):  
Edward J. Parish ◽  
Tsao-Yi Wei ◽  
Peter Livant
1995 ◽  
Vol 76 (1) ◽  
pp. 129-133 ◽  
Author(s):  
Edward J. Parish ◽  
Stephen A. Kizito ◽  
Jian Peng ◽  
Robert W. Heidepriem ◽  
Peter Livant

2011 ◽  
Vol 7 (3) ◽  
pp. 1434-1439
Author(s):  
Mona Boukthir ◽  
Fathi Zribi ◽  
Mohamed Belhouchet ◽  
Fakher Chabchoub

A series of pyrimidoquinazoline are prepared via the reaction of ethyl 2,2-dicyano-1-arylvinylcarbamate derivatives 1a-b with methyl 2-aminobenzoate, 1-(2-aminophenyl)ethanone and 2-aminobenzonitrile. The reactivity of compounds 1a-b toward 3-amino-4,6-diphénylnicotinonitrile are studied. The structures of the synthesized compounds are elucidated by X-ray diffraction, IR spectroscopy and nuclear magnetic resonance. 


1972 ◽  
Vol 50 (11) ◽  
pp. 1786-1788 ◽  
Author(s):  
R. N. Butler

The n.m.r. spectral properties of a range of the title compounds are reported and discussed.


1968 ◽  
Vol 46 (17) ◽  
pp. 2855-2859 ◽  
Author(s):  
Robert R. Fraser ◽  
K. E. Haque

The nuclear magnetic resonance and mass spectral behavior of 5-phenyltetrazole, 5-p-nitrophenyl-tetrazole and the 1-methyl and 2-methyl derivatives of each have been determined. Characteristic differences between the spectra of the 1-methyl and 2-methyl isomers have been noted and found to be useful for the purpose of structural assignments. The synthesis of 1- and 2-methyl-5-phenyltetrazole containing 47.5 % of 15N in the 1- and 4-positions of the tetrazole ring aided interpretation of the mass spectra and also allowed measurement of a geminal and a vicinal 15N—H coupling constant.


1970 ◽  
Vol 48 (3) ◽  
pp. 451-458 ◽  
Author(s):  
L. D. Hall ◽  
P. R. Steiner

The facile synthesis of 3,6-anhydro-5-deoxy-5-fluoro-1,2-O-isopropylidene-α-L-idofuranose (4) from readily available precursors is described. The 1H and 19F nuclear magnetic resonance spectra of this derivative have been analyzed. Interestingly, the fluorine substituent exhibits detectable spin coupling with all ring protons except H-2. Both of the anomeric 1,2-di-O-acetyl derivatives of (4) have also been studied.


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