Phenolic Analogs of Amino Carboxylic-Acid Ligands for Tc-99m. 1. Synthesis and Characterization of N,N'-Ethylenebis[2-(-O-Hydroxyphenyl)Glycines] (Ehpg)

1987 ◽  
Vol 40 (10) ◽  
pp. 1695 ◽  
Author(s):  
JG Wilson

Nine N,N'- ethylenebis [2-(o- hydroxyphenyl ) glycines ] ( ehpg ) have been prepared and characterized by conversion into their dimethyl ester dihydrochlorides. Their i.r ., 1H n.m.r. and f.a.b. mass spectral data are presented and discussed.

Author(s):  
Garima Shrivastava ◽  
Manjul Shrivastava

New Schiff base (2-[(1H-benzimidazol-2-ylimino) methyl]-4,6- diiodophenol) was synthesized by the condensation of aryl/hetero aromatic aldehyde (3,5diiodosalicylaldehyde) with 2- amino benzimidazole under conventional and microwave conditions and characterized through IR, HNMR and Mass spectral data and CHN analysis


1988 ◽  
Vol 41 (2) ◽  
pp. 173 ◽  
Author(s):  
JG Wilson

Ten N,N,- ethylenebis [N-(o- hydroxybenzyl ) glycines ] ( ehbg ), eight of them new, have been synthesized and characterized by their i.r ., 1H n.m.r . and f.a.b, mass spectra and by conversion of their dimethyl ester dihydrochlorides.


2020 ◽  
pp. 34-38
Author(s):  
Laxminarayana Eppakayala ◽  
Ravi Kumar Bommera ◽  
Sailaja Gummadelli ◽  
Thirumala Chary Maringanti

Some substituted benzoxazine derivatives have been synthesized in simple two steps. The structures of the synthesized compounds were confirmed by NMR and Mass spectral data.


1975 ◽  
Vol 53 (6) ◽  
pp. 939-944 ◽  
Author(s):  
Elmer C. Alyea ◽  
Abdul Malek

The synthesis and characterisation of several dibasic tridentate Schiff base ligands (H2SB) are described. Structural formulas for the isolated ligands are suggested on the basis of infrared, nuclear magnetic resonance, and mass spectral data.


1999 ◽  
Vol 54 (7-8) ◽  
pp. 534-541 ◽  
Author(s):  
Teruyuki Kobayashi ◽  
Yumiko Sasaki ◽  
Tetsuya Akamatsu ◽  
Toshihiro Ishii ◽  
Yoshiaki Oda ◽  
...  

Abstract The binuclear Co(II) and Mn(II) complexes with H5(HXTA). where H5(HXTA) repre­sents N,N′-(2-hydroxy-5-methyl-1,3-xylylene)bis(N-carboxymethylglycine), induced a strong ethylene evolution from 1-aminocyclopropane-l-carboxylic acid (ACC) in the presence of hydrogen peroxide, whereas activities of the corresponding Fe(III), Ni(II), and V(III) com­plexes were found negligible. Based on spectroscopic results and mass-spectral data it is proposed that a peroxide adduct of binuclear Co(II) (and Mn(II)) complex with η1-coordina­tion mode interacts with ACC, which is chelated to a binuclear cobalt complex leading to facile oxidative degradation of ACC and to evolution of ethylene.


Author(s):  
Nisheeth C. Desai ◽  
Tushar J. Karkar

The synthesis of a novel series of 6-((arylidene) amino)-2-oxo-1-((1-(2-oxo-2H-chromen-3-yl) ethylidene) amino)-4-phenyl-1,2-dihydropyridine-3,5-dicarbonitriles 4a-o were synthesized and structures of compounds have been elucidated by IR,1H NMR,13C NMR and mass spectral data. Antimicrobial activity was measured against certain strains of bacteria and fungi by serial broth dilution. Evaluation of antimicrobial activity shown that the compounds (4g, 4j, 4k and 4o) were found to be most active against selected bacterial strains and compounds (4d, 4m and 4n) were found to be most active against selected fungal strains.


2013 ◽  
Vol 1 (03) ◽  
pp. 12-19
Author(s):  
Alex Martin

The synthesis of 2-furyl-5-(substituted)-1,3,4-oxadiazoles was carried out by microwave irradiation of 2-furoic acid and ethanol followed by subsequent hydrazinolysis with hydrazine hydrate. Finally furan-2-acid hydrazide was treated with appropriate carboxylic acid in the presence of phosphorous oxychloride to produce title compounds. The structures of the newly synthesized compounds were established on the basis of spectral analysis such as IR, H1NMR and Mass spectral data. The synthesized compounds were screened for their anti-tubercular activity.


2018 ◽  
Vol 13 (4) ◽  
pp. 1934578X1801300
Author(s):  
Venkata Sai Prakash Chaturvedula ◽  
Srinivasa Rao Meneni

A new diterpene glycoside with six β-D-glucopyranosyl units was isolated from the extract of the leaves of Stevia rebaudiana Bertoni, which was identified as 13-[(2- O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy] ent-kaur-16-en-19-oic acid-[2- O-β-D-glucopyranosyl-3- O-(2- O-β-D-glucopyranosyl)-β-D-glucopyrano-syl -β-D-glucopyranosyl) ester (1) based on the extensive NMR (1H and 13C, COSY, HSQC, and HMBC) and mass spectral data as well as hydrolysis studies.


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