Effect of ortho- and para-chlorine substitution on hydroxychlorochalcone

2021 ◽  
Vol 27 (2) ◽  
Author(s):  
Rogério F. Costa ◽  
Antônio S. N. Aguiar ◽  
Igor D. Borges ◽  
Ricardo Ternavisk ◽  
Clodoaldo Valverde ◽  
...  
1984 ◽  
Vol 39 (10) ◽  
pp. 1427-1432
Author(s):  
Edgar Streich ◽  
Anton Rieker

Chlorination of the di-tert-butylation product of 2-naphthol leads to 3,6-di-tert-butyl-1,1-dichloro- l,2-dihydronaphthalen-2-one (4a) instead of 1,6-di-tert-butyl-1,3-dichloro-1,2-dihydronaphthalen-2-one (2) as reported [2], The structural proof was mainly offered by 13C NMR spectroscopy. The influence of annelation and chlorine substitution in 1,2-dihydronaphthalen-2-ones on δ13c=o is discussed, which is of importance for the use of δ13c=o for a general discrimination between ortho- and para-quinolide structures.


1981 ◽  
Vol 59 (20) ◽  
pp. 2940-2949 ◽  
Author(s):  
R. Garth Kidd ◽  
H. Garth Spinney

The seven hexahaloantimonate anions in the series [SbClnBr6−n]− have been prepared and their antimony-121 nmr spectra show that for [SbCl4Br2]−, [SbCl3Br3]−, and [SbCl2Br4]−, only the cis isomers are present in acetonitrile solution. The pairwise additivity model for central atom shielding has been used for configuration assignments. Models relevant to the higher incidence of cis over trans isomers are discussed. The nuclear shielding of 121Sb is the most sensitive to halogen substitution of all the elements whose halide chemical shifts have been studied. Antimony shieldings exhibit normal halogen dependence, with bromine substitution causing upfield shifts relative to chlorine substitution.


2016 ◽  
Vol 113 ◽  
pp. 610-625 ◽  
Author(s):  
Franziska Naporra ◽  
Susanne Gobleder ◽  
Hans-Joachim Wittmann ◽  
Julia Spindler ◽  
Michael Bodensteiner ◽  
...  

MedChemComm ◽  
2018 ◽  
Vol 9 (7) ◽  
pp. 1164-1171 ◽  
Author(s):  
Chandrani Nath ◽  
Vishnu Nayak Badavath ◽  
Abhishek Thakur ◽  
Gulberk Ucar ◽  
Orlando Acevedo ◽  
...  

Chlorine substitution on a 3,5-diphenyl-pyrazoline derivative enabled potent and selective inhibition of hMAO-A; calculations suggest an “aromatic sandwich” orientation is responsible.


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