Wszystkie pola: Shah, M. - Katalog OPAC zbiorów

Skocz do pozycji: 1.

Tytuł:: Synthesis and Characterization of Cu(II), Ni(II) and Co(II) Based Schiff Base Complexes
Autorzy:: Bhalu, A.
Vilapara, K.
Maru, M.
Shah, M.
Powiązania:: https://bibliotekanauki.pl/articles/412444.pdf
Data publikacji:: 2014
Wydawca:: Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:: schiff base
metal complexes
Opis:: N-(3-Bromo-4-hydroxy-5-methoxybenzylidene)-4-Bromobenzenamine was synthesized. This was further used to synthesize Co(II), Ni(II) and Co(II) based metal complexes and characterized by FT-IR, Elemental analysis, ESI Mass and UV spectroscopy.
Źródło:: International Letters of Chemistry, Physics and Astronomy; 2014, 12; 51-55
2299-3843
Pojawia się w:: International Letters of Chemistry, Physics and Astronomy
Dostawca treści:: Biblioteka Nauki

Artykuł

Skocz do pozycji: 2.

Tytuł:: Reusable Nanocatalyst: Zirconia and Sulfated Zirconia
Autorzy:: Gondaliya, M. B.
Maheta, T.
Mamtora, M. J.
Shah, M. K.
Powiązania:: https://bibliotekanauki.pl/articles/411589.pdf
Data publikacji:: 2014
Wydawca:: Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:: Nanocatalyst
nanoparticles
Sulfated Zirconia
synthesis
Benzodiazepines
solid catalyst
solvent-free
green chemistry
Opis:: 1,5-benzodiazepines have been synthesized by Nano Zirconia and Nano Sulfated Zirconia in solvent free conditions. Synthesis was carried out by conventional as well as microwave method. Benzodiazepines were synthesized by reacting o-phenylenediamine and few ketones in the presence of catalytic amount of Nanoparticles. Particles used were sized in between 53-100 nm. Nanoparticles were characterized by FT-IR, DLS and powder XRD analysis.
Źródło:: International Letters of Chemistry, Physics and Astronomy; 2014, 17, 3; 295-302
2299-3843
Pojawia się w:: International Letters of Chemistry, Physics and Astronomy
Dostawca treści:: Biblioteka Nauki

Artykuł

Skocz do pozycji: 3.

Tytuł:: Synthesis and antimicrobial screening of some new pyrimido[1,2-a]benzimidazole derivatives
Autorzy:: Shah, N. M.
Joshi, H. S.
Powiązania:: https://bibliotekanauki.pl/articles/411967.pdf
Data publikacji:: 2014
Wydawca:: Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:: 2-aminobenzimidazole
pyrimido[1,2-a]benzimidazole
chalcone
antimicrobial activity azoloazine
Opis:: Some new pyrimido[1,2-a]benzimidazole derivatives were synthesized by reacting 2-amino benzimidazole and chalcones in n-butanol at reflux temperature. In our present study we have used various heterocyclic chalcones derived from furfural and substituted acetophenones. All synthesized compounds were characterized by IR, 1H NMR and Mass spectroscopy. All synthesized compounds were screened for their antimicrobial activity against gram positive and gram negative bacteria which showed moderate to good activity.
Źródło:: International Letters of Chemistry, Physics and Astronomy; 2014, 6; 56-60
2299-3843
Pojawia się w:: International Letters of Chemistry, Physics and Astronomy
Dostawca treści:: Biblioteka Nauki

Artykuł

Skocz do pozycji: 4.

Tytuł:: A rapid, convient and diversified-multicomponent synthesis and characterization of pyrano[2,3-b]indoles
Autorzy:: Ghodasara, H. B.
Singala, P. M.
Shah, V. H.
Powiązania:: https://bibliotekanauki.pl/articles/412134.pdf
Data publikacji:: 2014
Wydawca:: Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:: 1,3-bifunctional synthon
Pyrano[2,3-b]indoles
multi component reaction
non-chromatographic metod
Opis:: A series of pyrano[2,3-b]indoles, was efficiently synthesized via one-pot, multi component reaction (MCRs) of 1,3-bifunctional synthon(malononitrile/ethylcyano acetate), aromatic aldehydes and oxiindole in the presence of various basic catalyst. The key advantages of this process are high yields, shorter reaction times, easy work-up, and purification of products by non-chromatographic method.
Źródło:: International Letters of Chemistry, Physics and Astronomy; 2014, 7; 69-76
2299-3843
Pojawia się w:: International Letters of Chemistry, Physics and Astronomy
Dostawca treści:: Biblioteka Nauki

Artykuł

Skocz do pozycji: 5.

Tytuł:: Synthesis of novel 2-mercapto-4-(p-aminophenyl sulphonylamino)-6-(aryl)-pyrimidine-5-carboxamide derivatives via the Biginelli reaction
Autorzy:: Bhuva, N. H.
Gothalia, V. K.
Singala, P. M.
Talpara, P. K.
Faldu, V. J.
Shah, V. H.
Powiązania:: https://bibliotekanauki.pl/articles/412069.pdf
Data publikacji:: 2014
Wydawca:: Przedsiębiorstwo Wydawnictw Naukowych Darwin / Scientific Publishing House DARWIN
Tematy:: 2-mercapto-4-(p-aminophenylsulphonylamino)-6-(aryl)-pyrimidine-5-carboxamide
Biginelli condensation
Opis:: Series of 2-mercapto-4-(p-aminophenylsulphonylamino)-6-(aryl)-pyrimidine-5-carboxamide Aa-h were synthesized via the biginelli condensation. 2-mercapto-4-amino-6-(aryl)-pyrimidine-5-carboxamide react with p-acetamidophenylsulphonylchloride in the presence of pyridine 2 to form 2-mercapto-4-(p-acetamidophenylsulphonylamino)-6-(aryl)-pyrimidine-5-carboxamide 3. It was treated with diluted HCl under reflux afforded 2-mercapto-4-(p-aminophenylsulphonylamino)-6-(aryl)-pyrimidine-5-carboxamide A_a-h. The newly synthesized compounds were characterized by elemental analyses, infrared (IR), ¹H NMR and ¹³ C NMR spectroscopic investigation.
Źródło:: International Letters of Chemistry, Physics and Astronomy; 2014, 17, 2; 168-173
2299-3843
Pojawia się w:: International Letters of Chemistry, Physics and Astronomy
Dostawca treści:: Biblioteka Nauki

Artykuł

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