Potential antipsychotic agents. 7. Synthesis and antidopaminergic properties of the atypical highly potent (S)-5-bromo-2,3-dimethoxy-N-[(1-ethyl-2-pyrrolidinyl)methyl]benzamide and related compounds. A comparative study

1990 ◽  
Vol 33 (8) ◽  
pp. 2305-2309 ◽  
Author(s):  
Thomas Hoegberg ◽  
Tomas De Paulis ◽  
Lars Johansson ◽  
Yatendra Kumar ◽  
Haakan Hall ◽  
...  
Keyword(s):  
Comparative Study ◽  
Antipsychotic Agents ◽  
Related Compounds

scholarly journals Comparative Study of Naphthoquinone Contents of Selected Greek Endemic Boraginaceae Plants - Antimicrobial Activities

2017 ◽  
Vol 12 (2) ◽  
pp. 1934578X1701200
Author(s):  
Teisa Tufa ◽  
Harilaos Damianakos ◽  
Konstantia Graikou ◽  
Ioanna Chinou
Keyword(s):  
Antimicrobial Activity ◽  
Nmr Spectroscopy ◽  
Comparative Study ◽  
Pathogenic Fungi ◽  
2D Nmr ◽  
Antimicrobial Activities ◽  
2D Nmr Spectroscopy ◽  
Chromatographic Separations ◽  
Esi Ms ◽  
Related Compounds

The cyclohexane (Ch) extracts of the roots of five Greek endemic Boraginaceae plants, Onosma kaheirei Teppner, O. graeca Boiss., O. erecta Sibth. & Sm., Alkanna sfikasiana Kit Tan, Vold and Strid and Cynoglossum columnae Ten, were investigated for the presence of alkannin/shikonin-related compounds. All species, s except C. columnae and O. erecta, were found to contain this type of compounds. Seven compounds were obtained after several chromatographic separations from the Ch extracts of the investigated plants: deoxyalkannin (1), 2″-( S)- α-methylbutyrylalkannin (2), isobutyrylalkannin (3), propionylalkannin (4), acetylalkannin (5), β-hydroxyisovalerylalkannin (6), and β,β-dimethylacrylalkannin (7). All structures were identified by 1D 1H-/13C- and 2D NMR spectroscopy, assisted also by ESI-MS. The extracts and the isolated compounds exhibiting an interesting antimicrobial profile when evaluated for their antimicrobial activity against six Gram-positive and -negative bacteria and three human pathogenic fungi.

Lignin and related compounds. I. A comparative study of catalysts for lignin hydrogenolysis

1969 ◽  
Vol 47 (5) ◽  
pp. 723-727 ◽  
Author(s):  
J. M. Pepper ◽  
Y. W. Lee
Keyword(s):  
Comparative Study ◽  
Raney Nickel ◽  
Lignin Degradation ◽  
Soluble Fraction ◽  
Degradation Products ◽  
Quantitative Estimation ◽  
Liquid Chromatographic Separation ◽  
Lignin Degradation Products ◽  
Liquid Chromatographic ◽  
Related Compounds

A detailed comparative study has been made of the effectiveness of various catalysts for the hydrogenolysis of spruce wood lignin. The catalysts studied were Raney nickel, 10% palladium–charcoal, 5% rhodium–charcoal, 5% rhodium–alumina, 5% ruthenium–charcoal, and 5% ruthenium–alumina. Lignin degradation products were obtained initially as a chloroform-soluble fraction which was then divided and studied as diethyl ether-soluble and -insoluble fractions. Gas–liquid chromatographic separation of the ether-soluble fraction made possible the characterization and quantitative estimation of many of the lower molecular weight lignin degradation products.The data indicate that rhodium, palladium, and a limited amount of Raney nickel produce similar results as do ruthenium and an excess of Raney nickel; however, with the latter catalysts the degradation is more severe. In particular, rhodium–charcoal and palladium–charcoal appear to offer interesting advantages as catalysts for lignin hydrogenolysis.

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