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Molbank, Volume 2006, Issue 4 (June 2006)

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Open AccessShort Note Synthesis of novel 2-(2-(6-chloro-9H-purin-9-yl)ethoxy)-6-isobutoxy-tetrahydro-2H-pyran-3-ol as a potential antiviral agent
Molbank 2006, 2006(4), M481; doi:10.3390/M481
Received: 18 October 2005 / Accepted: 16 March 2006 / Published: 1 June 2006
PDF Full-text (195 KB) | Supplementary Files
Abstract In this paper we propose the synthesis of 2-(2-(6-chloro-9H-purin-9-yl)ethoxy)-6-isobutoxy-tetrahydro-2H-pyran-3-ol as a new potential antiviral agent Its structure has been confirmed by IR, 1H-NMR, 13C-NMR, UV and Mass spectroscopic data. Full article
Open AccessShort Note 1,1’-dibenzyl-5,5’-diphenyl-3,3’-bipyrazole
Molbank 2006, 2006(4), M482; doi:10.3390/M482
Received: 24 October 2005 / Accepted: 15 January 2006 / Published: 1 June 2006
PDF Full-text (148 KB) | Supplementary Files
Open AccessShort Note N,N-bis[(1,5-dimethylpyrazol-3-yl)methyl]para-toluidine
Molbank 2006, 2006(4), M483; doi:10.3390/M483
Received: 24 October 2005 / Accepted: 15 January 2006 / Published: 1 March 2006
PDF Full-text (135 KB) | Supplementary Files
Open AccessShort Note Synthesis, Physical Characterization, Antibacterial and Antifungal activities of a novel bis(3-((E)-1-(2-hydroxyphenyl)ethylideneamino)phenyl)methanone
Molbank 2006, 2006(4), M484; doi:10.3390/M484
Received: 13 January 2006 / Accepted: 3 March 2006 / Published: 1 June 2006
PDF Full-text (245 KB) | Supplementary Files
Abstract
Bis (3-((E)-1-(2-hydroxyphenyl) ethylideneamino) phenyl) methanone has been synthesized in this paper and its structure was confirmed by 1H-NMR, 13C-NMR, IR and Mass spectra. Its AM1 and B3LYP/6-31G* calculations to characterize the physical properties of this molecule has been also presented. Finally, the [...] Read more.
Bis (3-((E)-1-(2-hydroxyphenyl) ethylideneamino) phenyl) methanone has been synthesized in this paper and its structure was confirmed by 1H-NMR, 13C-NMR, IR and Mass spectra. Its AM1 and B3LYP/6-31G* calculations to characterize the physical properties of this molecule has been also presented. Finally, the antifungal and antibacterial activities of this derivative have been evaluated. Full article

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