An X-ray crystallographic, 1H nuclear magnetic resonance, and MNDO SCF-MO conformational study of o-substituted N-benzylbenzothiohydroxamic acids

Author(s):  
Ana M. Lobo ◽  
Sundaresan Prabhakar ◽  
M. Amelia Santos ◽  
Henry S. Rzepa ◽  
David J. Williams
1988 ◽  
Vol 66 (7) ◽  
pp. 1546-1551 ◽  
Author(s):  
Vanga S. Rao ◽  
Jean-Paul Daris ◽  
Marcel Menard

The phenyl group is shown as a useful probe in sensing the environment in the 1H nuclear magnetic resonance conformational study of a variety of quaternary heteroaromatic carbapenem derivatives. The influence of the -SCH2- substituent in determining the site of quaternization in nitrogen-containing heteroaromatic compounds is demonstrated through the acidity measurements of these methylene protons.


2021 ◽  
Author(s):  
Guang-Wei Zhang ◽  
Jia-Yin XIANG ◽  
Tao-Tao Zhong ◽  
Xin-Ru ZHI ◽  
Chuang Gao ◽  
...  

This article reports a pair of rigid iodide ion macrocyclic receptors of syn/anti configurations. Single crystal X-ray analysis confirms the structure of the syn-isomers, 1H Nuclear Magnetic Resonance (1H NMR)...


1976 ◽  
Vol 54 (7) ◽  
pp. 1135-1138 ◽  
Author(s):  
José Elguero ◽  
Alain Fruchier ◽  
Georges Llouquet ◽  
Claude Marzin

From a 1H nmr study it has been possible to show that the eight-membered ring of the N,N′-disubstituted 3,4-dihydro-1,6-benzodiazocine-2,5-diones has a boat conformation, the interconversion barrier of which is slightly over 100 kJ/mol.


1979 ◽  
Vol 34 ◽  
pp. 87-90 ◽  
Author(s):  
Gerard Folcher ◽  
Pierrette Charpin ◽  
Rose-Marie Costes ◽  
Nelly Keller ◽  
George C.de Villardi

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