Preparative, mechanistic and tautomeric investigation of 1-phenyl and 1-methyl derivative of 3-methyl-5-pyrazolone

2021 ◽  
Vol 133 (2) ◽  
Author(s):  
Hossein Fakhraian ◽  
Yaser Nafari
Keyword(s):  
1988 ◽  
Vol 53 (8) ◽  
pp. 1806-1811 ◽  
Author(s):  
Zdeněk Polívka ◽  
Jan Metyš ◽  
Miroslav Protiva

Reactions of 11-chloro-6,11-dihydrodibenzo[b,e]thiepin and its 2-methyl derivative, and further of the methanesulfonates of 2-chloro- and 2-bromo-6,11-dihydrodibenzo[b,e]thiepin-11-ol with 3-quinuclidinol afforded the title ethers I-IV. The 2-methyl compound II (VÚFB-17 088) showed significant antihistamine activity and the 2-chloro compound III (VÚFB-17 089), having antireserpine and anticataleptic activity, proved a potential antidepressant agent.


Author(s):  
Jeroen A. van Bokhoven ◽  
Andrea N. Blankenship ◽  
Manoj Ravi ◽  
Mark A. Newton

Langmuir ◽  
1996 ◽  
Vol 12 (20) ◽  
pp. 4966-4968 ◽  
Author(s):  
Jan Czapkiewicz ◽  
Patrycja Dynarowicz ◽  
Piotr Milart

1992 ◽  
Vol 33 (20) ◽  
pp. 2825-2828 ◽  
Author(s):  
Shigeyasu Kuroda ◽  
Jun-ichi Yazaki ◽  
Sunao Maeda ◽  
Kazuo Yamazaki ◽  
Masaki Yamada ◽  
...  
Keyword(s):  

1977 ◽  
Vol 8 (46) ◽  
pp. no-no
Author(s):  
P. K. BRIDSON ◽  
W. MARKIEWICZ ◽  
C. B. REESE
Keyword(s):  

1977 ◽  
Vol 8 (31) ◽  
pp. no-no
Author(s):  
P. HASSANALY ◽  
H. J. M. DOU ◽  
J. METZGER ◽  
G. ASSEF ◽  
J. KISTER

2009 ◽  
Vol 62 (9) ◽  
pp. 1062 ◽  
Author(s):  
Jiong Ran ◽  
Ming Wah Wong

Conformations of 4,4-bisphenylsulfonyl-N,N-dimethylbutylamine (BSDBA) were examined by ab initio calculations. Intramolecular C–H···N, C–H···O, and π···π interactions are found to play an important role in governing the conformational properties. This finding is supported by charge density analysis based on the theory of atoms in molecules. The calculated molecular structure and 1H chemical shifts of the methyl derivative (BSTBA) are in excellent agreement with experimental findings. The intramolecular C–H···N hydrogen bond in BSDBA is estimated to have a significant interaction energy of 25 kJ mol–1. The sulfonyl oxygens in BSDBA interact readily with neighbouring methylene, methyl and phenyl hydrogens via C–H···O=S hydrogen bonds. In agreement with experiment, solvent effect calculations indicate that these weaker intramolecular interactions prevail in an aprotic polar medium.


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