scholarly journals Synthesis of Novel S-Glucosides Containing 5-Methylisoxazole Substituted 1,2,4-Triazole

2013 ◽  
Vol 2013 ◽  
pp. 1-4
Author(s):  
Shujun Chao ◽  
Yingling Wang
Keyword(s):  
Spectral Data ◽  
Potassium Hydroxide ◽  
Elemental Analyses

Nine new S-β-D-glucosides containing 4-aryl-5-(5-methylisoxazol-3-yl)-1,2,4-triazol-3-thiols have been synthesized by the direct glycosylation of 4-aryl-5-(5-methylisoxazol-3-yl)-1,2,4-triazol-3-thiols with 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide in ethanol in the presence of potassium hydroxide followed by deacetylation using dry ammonia in dry methanol. All the compounds synthesized have been characterized by their elemental analyses and spectral data.

scholarly journals Synthesis and Biological Evaluation of Some New Chalcones Containing 2,5-Dimethylfuran Moiety

2011 ◽  
Vol 8 (2) ◽  
pp. 541-546 ◽  
Author(s):  
S. Sridhar ◽  
S. C. Dinda ◽  
Y. Rajendra Prasad
Keyword(s):  
Aqueous Solution ◽  
Spectral Data ◽  
Potassium Hydroxide ◽  
Room Temperature ◽  
Aromatic Aldehydes ◽  
Biological Evaluation ◽  
Significant Activity ◽  
H Nmr ◽  
Elemental Analyses ◽  
Synthesis And Biological Evaluation

A series of new chalcones(3a-g)were prepared by Claisen-Schmidt condensation of 3-acetyl-2,5-dimethylfuran with various substituted aromatic aldehydes in presence of aqueous solution of potassium hydroxide and ethanol at room temperature. The synthesized chalcones were characterized by means of their IR,1H NMRspectral data and elemental analyses. When these chalcones were evaluated for antimicrobial and anti-inflammatory activities, some of them were found to possess significant activity, when compared to standard drugs.

Azaoxa Macrocyclic and Acyclic Complexesof Lanthanides

1998 ◽  
Vol 63 (3) ◽  
pp. 363-370 ◽  
Author(s):  
Violetta Patroniak-Krzyminiewska ◽  
Wanda Radecka-Paryzek
Keyword(s):  
Schiff Base ◽  
Spectral Data ◽  
Macrocyclic Ligand ◽  
Lanthanide Ions ◽  
H Nmr ◽  
Elemental Analyses ◽  
Acyclic Complexes ◽  
Schiff Base Cyclocondensation

The template reactions of 2,6-diacetylpyridine with 3,6-dioxaoctane-1,8-diamine in the presence of dysprosium(III), thulium(III) and lutetium(III) chlorides and erbium(III) perchlorate produce the complexes of 15-membered macrocyclic ligand with an N3O2 set of donor atoms as a result of the [1+1] Schiff base cyclocondensation. In contrast, analogous reactions involving the lighter lanthanide ions (lanthanum(III), samarium(III) and europium(III)) yield the acyclic complexes with terminal acetylpyridyl groupings as products of the partial [2+1] condensation. The complexes were characterized by spectral data (IR, UV-VIS, 1H NMR, MS), and thermogravimetric and elemental analyses.

Synthesis of 4-(3-coumarinyl)-3-benzyl-4-thiazolin-2-one 4-methylbenzylidenehydrazone and determination of the isomeric structure by X-ray analysis

2003 ◽  
Vol 218 (12) ◽  
Author(s):  
Süheyla Özbey ◽  
Nilgün Karalı ◽  
Aysel Gürsoy
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Spectral Data ◽  
X Ray Diffraction ◽  
X Ray ◽  
Isomeric Structure ◽  
Elemental Analyses

AbstractIn this study 4-(3-coumarinyl)-3-benzyl-4-thi azolin-2-one 4-methylbenzylidenehydrazone 3 was synthesised. An independent proof of the thiazolylhydrazone structure of 3 was achieved by single crystal X-ray diffraction analysis. Elemental analyses and spectral data (IR,

scholarly journals Synthesis and Bio-Spectral Studies of Co(II) Complex of 5-Chloro-2,4-Dihydroxy Butyrophenoneoxime (CDHBOX)

2010 ◽  
Vol 6 (3) ◽  
pp. 1120-1133
Author(s):  
F. Rehman ◽  
M. Bhardwaj ◽  
U.K. Jetley
Keyword(s):  
Spectral Data ◽  
Standard Free Energy ◽  
Spectral Studies ◽  
Curvularia Lunata ◽  
Mass Spectral ◽  
Ir Studies ◽  
Free Energy Of Formation ◽  
Escherchia Coli ◽  
Elemental Analyses ◽  
Point Determination

Co(II) complex of 5-chloro-2,4-dihydroxy butyrophenoneoxime (CDHBOX) was synthesized from 5-chloro-2,4-dihydroxy butyrophenoneoxime by using standard protocol, and characterized by elemental analyses, melting point determination and spectral data. The ML2 (metal/ligand) stoichiometry of the complex was determined by spectrophotometric and potentiometric studies, and mass spectral data. The value of stability constant of the complex was found to be 6.94x 108 while its standard free energy of formation is 12.155 kcal/mol at 27ºC. Beer’s law is obeyed in the concentration range 2-15 ppm of Co. The value of molar extinction coefficient and sensitivity as per Sandell’s scale were found to 3.35x 103 L.mol-1cm-1and 0.017 μg Co/cm2 respectively. The value of activation energy and the Arrhenius constant Arrhenius constant were found as 4.949 kjmol-1, 74.39. The IR studies reveal that the phenolic proton is lost on complexation and the oxygen of the phenolic (–OH) and nitrogen of the oximino (=NOH) groups coordinate with Co(II) ion. The electronic spectra and magnetic susceptibility measurement indicate that the complex is paramagnetic and tetrahedral in nature. The antimicrobial activity of different concentrations of ligand and its Co(II)-complex  has been evaluated against Curvularia lunata, Fusarium oxysporum and Alternaria alternata fungi  and Streproproteus, Staph, Escherchia coli, Klebsella, and pseudomonas bacteria. The results indicated that the ligand (CDHBOX) and its Co(II) complex have good anti-microbial properties. 

Heterocyclic Synthesis Using Nitrilimines: Part 9. Synthesis of New 1,3,4-Thiadiazin-5-one Derivatives

2008 ◽  
Vol 63 (5) ◽  
pp. 585-590 ◽  
Author(s):  
Hany M. Dalloul ◽  
El-Hossain A. R. Mohamed ◽  
Ali Z. El-Shorafa
Keyword(s):  
Spectral Data ◽  
Intramolecular Cyclization ◽  
Heterocyclic Synthesis ◽  
Hydrazonoyl Halides ◽  
Elemental Analyses

A series of new 3,5,6-thiadiaza-4-hexenoates (4a - k) were synthesized from the reaction of the corresponding hydrazonoyl halides 1 with ethyl mercaptoacetate (3). These compounds underwent intramolecular cyclization to 1,3,4-thiadiazin-5-one derivatives (5a - k) in the presence of MeONa or LiH. The structures of the synthesized compounds were confirmed by their elemental analyses and spectral data.

Die oxidative Addition von NickeI(0)-KompIexen an Kohlenstoff-Kohlenstoff-Bindungen im Cyclobutadien. Zur Frage der Überführbarkeit von Cyclobutadien-Nickel(O)-Komplexen in Nickelaringe / Oxidative Addition of Nickel(O) Complexes to Carbon-Carbon Bonds in Cyclobutadiene. The Question of the Interconvertibility of Cyclobutadiene-nickel(O) Complexes and the Nickelaring Systems

1985 ◽  
Vol 40 (5) ◽  
pp. 624-635 ◽  
Author(s):  
John J. Eisch ◽  
Andrzej M. Piotrowski ◽  
Allen A. Aradi ◽  
Carl Krüger ◽  
Maria J. Romão
Keyword(s):  
Spectral Data ◽  
Structure Determination ◽  
Oxidative Addition ◽  
Subsequent Treatment ◽  
X Ray ◽  
X Ray Crystallography ◽  
Carbon Carbon Bonds ◽  
Elemental Analyses ◽  
Carbon Bonds

Abstract Bis(triethylphosphine)(η4-tetraphenylcyclobutadiene)nickel (4) was synthesized by the reduction of (η4-tetraphenylcyclobutadiene)nickel(II)bromide (3) with t-butyllithium in the presence of Et3P, and its structure was determined by X-ray crystallography. Furthermore, its reactivity towards CO, CH3CO2H, PhC≡CPh, LiAlH4 and O2 were investigated. 1,1-Bis(triethylphos-phine)-2,3,4,5-tetraphenylnickelole (14) was synthesized from (E,E)-1,4-dilithio-1,2,3,4-tetraphenyl-1,3-butadiene (15) and bis(triethylphosphine)nickel(II)bromide. Since the resulting crystals of the nickelole were not suitable for X-ray structure determination, the compound was characterized by elemental analyses, spectral data and carbonylation to yield tetraphenylcyclo-pentadienone (6).Analogous reductions of (η4 -tetraphenylcyclobutadiene)nickel(II)bromide (3) in the presence of Ph3P or Ph2PCH2CH2PPh2 , followed by carbonylation, led to 6 in 40% yield, demonstrating that about half of the cyclobutadiene rings in 3 undergo cleavage upon reduction to give the nickelole.Reactions of the dilithium reagent 15 with NiBr2 complexed with Me2PCH2CH2PMe2 ,Ph3P or Et2PCH2CH2PEt2 , led to the formation of thermolabile nickeloles, as demonstrated by carbonylàtion which yielded 6. Warming of the nickeloles and subsequent treatment with CH3CO2H led to the formation of 1,2,3,4,5,6,7,8-octaphenyl-1,3,5,7-octatetraene (8) and, in one case, octaphenyl-cyclooctatetraene (5).The relevance of these findings to the mechanism of the Reppe nickel-catalyzed oligomerization of alkynes is discussed.

Synthesis of 2-methyl-3-(1-aryl-1H-tetrazol-5-yl)-1,8-naphthyridines

1988 ◽  
Vol 53 (7) ◽  
pp. 1539-1542 ◽  
Author(s):  
Kaleru Mogilaiah ◽  
Kamreddy Rajendar Reddy ◽  
Gurram Rama Rao ◽  
Bathula Sreenivasulu
Keyword(s):  
Spectral Data ◽  
Phosphorus Pentachloride ◽  
Elemental Analyses ◽  
Imidoyl Chlorides

2-Methyl-3-(1-aryl-1H-tetrazol-5-yl)-1,8-naphthyridines III have been synthesized by the reaction of 2-methyl-N-aryl-1,8-naphthyridine-3-carboxyamides (I) with phosphorus pentachloride and azidolysis of the resulting imidoyl chlorides. Structures of these compounds have been established by means of their elemental analyses and spectral data.

Chelates of nickel(II) and copper(II) with tridentate Schiff base formed by the condensation of S-benzyldithiocarbazate with benzoin

1978 ◽  
Vol 56 (15) ◽  
pp. 2000-2002 ◽  
Author(s):  
M. T. H. Tarafder ◽  
M. Akbar Ali
Keyword(s):  
Schiff Base ◽  
Spectral Data ◽  
General Formula ◽  
Schiff Base Ligand ◽  
Nickel Complexes ◽  
Planar Structure ◽  
Spectral Studies ◽  
Square Planar ◽  
Elemental Analyses ◽  
Tridentate Schiff Base

New complexes with the Schiff base ligand derived from S-benzyldithiocarbazate (NH2—NH—CSSCH2C6H5) have been prepared and characterized by elemental analyses, magnetic, conductometric, ir, and electronic spectral studies. The tridentate ONS Schiff base S-benzyl-β-N-(phenyl, phenylhydroxymethyl)methylenedithiocarbazate gave mono-ligand complexes with Ni(II) and Cu(II) having the general formula [MligandX] (M = Ni(II) and Cu(II); X = NO3, Cl, Br, NCS). A proposed square-planar structure for the nickel complexes is supported by magnetic and spectral data. A square-planar structure is also suggested for Cu(II) complexes. The ir results give evidence of the different bondings present in the complexes.

scholarly journals First synthesis of meso-substituted pyrrolo[1,2-a]quinoxalinoporphyrins

2014 ◽  
Vol 10 ◽  
pp. 808-813 ◽  
Author(s):  
Dileep Kumar Singh ◽  
Mahendra Nath
Keyword(s):  
Nitro Group ◽  
Spectral Data ◽  
Aromatic Aldehydes ◽  
Elemental Analyses ◽  
Porphyrin Analogues

A synthetic protocol for the construction of new meso-substituted pyrrolo[1,2-a]quinoxalinoporphyrins is described starting from 5-(4-amino-3-nitrophenyl)-10,15,20-triphenylporphyrin. The reaction of this porphyrin with 2,5-dimethoxytetrahydrofuran, followed by the reduction of the nitro group in the presence of NiCl2/NaBH4 afforded 5-(3-amino-4-(pyrrol-1-yl)phenyl)-10,15,20-triphenylporphyrin. This triphenylporphyrin underwent a Pictet–Spengler cyclization after the reaction with various aromatic aldehydes followed by in situ KMnO4 oxidation to form target porphyrin analogues in good yields. The structures of all synthesized products were established on the basis of spectral data and elemental analyses.

scholarly journals Synthetic, structural and antifungal studies of coordination compounds of Ru(III), Rh(III) and Ir(III) with tetradentate schiff bases

2006 ◽  
Vol 71 (8-9) ◽  
pp. 917-928 ◽  
Author(s):  
V.K. Sharma ◽  
Ankita Srivastava ◽  
Shipra Srivastava
Keyword(s):  
Spectral Data ◽  
Schiff Bases ◽  
Magnetic Moment ◽  
Coordination Compounds ◽  
Mass Spectra ◽  
Thermal Analyses ◽  
Agar Plate ◽  
Plate Method ◽  
Elemental Analyses ◽  
Fab Mass Spectra

A series of octahedral Ru(III), Rh(III) and Ir(III) complexes have been prepared with tetradentate Schiff bases derived by condensing isatin with 1,2-diaminoethane, 1,3-diaminopropane, 1,4-diaminobutane, 1,2-diaminobenzene and 1,3-diaminobenzene. The obtained complexes were characterized on the basis of their elemental analyses, magnetic moment, conductance, IR electronic, 1HNMR and FAB mass spectra, as well as thermal analyses. The Ru(III) complexes are low spin paramagnetic, while Rh(III) and Ir(III) behave as diamagnetic complexes. The IR spectral data revealed that all the Schiff bases behave as tetradentate and are coordinated to Ru(III), Rh(III) and Ir(III) via nitrogen and oxygen. Antifungal studies of the ligands as well as their complexes were carried out by the agar plate method.

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