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Molbank, Volume 2005, Issue 3 (September 2005)

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Open AccessShort Note 3-(2,5-Bis-dodecyl-4-iodo-phenylethynyl)-[1,10]-phenanthroline
Molbank 2005, 2005(3), M416; https://doi.org/10.3390/M416
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
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Abstract
The experimental procedure follows a protocol developed by Sonogashira [1].[...] Full article
Open AccessShort Note 3-(2,5-Bis-dodecyloxy-4-iodo-phenylethynyl)-[1,10]-phenanthroline
Molbank 2005, 2005(3), M417; https://doi.org/10.3390/M417
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (139 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Sonogashira [1].[...] Full article
Open AccessShort Note 3-(2,5-Bis-hexyloxy-4-iodo-phenylethynyl)-[1,10]-phenanthroline
Molbank 2005, 2005(3), M418; https://doi.org/10.3390/M418
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (136 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Sonogashira [1].[...] Full article
Open AccessShort Note 3-(2,5-Dibutoxy-4-iodo-phenylethynyl)-[1,10]-phenanthroline
Molbank 2005, 2005(3), M419; https://doi.org/10.3390/M419
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (143 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Sonogashira [1].[...] Full article
Open AccessShort Note 3-(2,5-Diethoxy-4-iodo-phenylethynyl)-[1,10]-phenanthroline
Molbank 2005, 2005(3), M420; https://doi.org/10.3390/M420
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (140 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Sonogashira [1].[...] Full article
Open AccessShort Note 3-(2,5-Diethyl-4-iodo-phenylethynyl)-[1,10]-phenanthroline
Molbank 2005, 2005(3), M421; https://doi.org/10.3390/M421
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (138 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Sonogashira [1].[...] Full article
Open AccessShort Note 3-(2,5-Dihexyl-4-iodo-phenylethynyl)-[1,10]-phenanthroline
Molbank 2005, 2005(3), M422; https://doi.org/10.3390/M422
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (137 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Sonogashira [1].[...] Full article
Open AccessShort Note 3,8-Bis-trimethylsilanylethynyl-[1,10]-phenanthroline
Molbank 2005, 2005(3), M423; https://doi.org/10.3390/M423
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (127 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Sonogashira [1] and recently used for the preparation of macrocyclic phenanthrolines [2].[...] Full article
Open AccessShort Note 3,8-Diethynyl-[1,10]-phenanthroline
Molbank 2005, 2005(3), M424; https://doi.org/10.3390/M424
Received: 13 June 2005 / Accepted: 8 August 2005 / Published: 1 September 2005
PDF Full-text (124 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
The experimental procedure follows a protocol developed by Eaborn [1].[...] Full article
Open AccessShort Note Synthesis of methyl N'-[1-(4-hydroxybutyl)-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl]-N-phenylimidothiocarbamate
Molbank 2005, 2005(3), M425; https://doi.org/10.3390/M425
Received: 17 May 2004 / Accepted: 21 May 2004 / Published: 1 August 2005
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Abstract
The desired compound 2 was obtained by complete deacetylation of compound 1 [1] using triethylamine [2].[...] Full article
Open AccessShort Note 1-Hydroxymethyl-3,5-diphenylpyrazole
Molbank 2005, 2005(3), M426; https://doi.org/10.3390/M426
Received: 20 May 2004 / Accepted: 9 July 2004 / Published: 1 August 2005
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Abstract
To a solution of 3,5-diphenylpyrazole 1 [1] (200 mg, 0.90 mmol) in ethanol (10 mL) was added formaldehyde 2 (110 mg, 1.28 mmol, 35 %) and the mixture was refluxed for two hours [2,3].[...] Full article
Open AccessShort Note 1-Hydroxymethyl-3-phenyl-5-methylpyrazole
Molbank 2005, 2005(3), M427; https://doi.org/10.3390/M427
Received: 20 May 2004 / Accepted: 9 July 2004 / Published: 1 August 2005
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Abstract
To a solution of 3-phenyl-5-methylpyrazole 1 [1] (7.11 g, 45 mmol) in ethanol (60 mL) was added formaldehyde 2 (3.85 g, 45 mmol, 35 %) and the mixture was refluxed for 90 minutes [2,3].[...] Full article
Open AccessShort Note Bis-(1-phenyl-5-nitro-6-methylthio-1,2,3,4-tetrahydropyrimidinyl)benzene and Bis-(1-phenyl-5-nitro-6-methylthio-1,2,3,4-tetrahydropyrimidinyl)diphenyl
Molbank 2005, 2005(3), M428; https://doi.org/10.3390/M428
Received: 21 May 2004 / Accepted: 1 June 2004 / Published: 1 August 2005
PDF Full-text (121 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
In continuation with our on going program on the synthesis of tetrahydropyrimidines [1,2], we have recently reported the synthesis of Bis-tetrahydropyrimidines [3] in which the rings are linked through flexible aliphatic chains.[...] Full article
Open AccessShort Note Synthesis of 3-[(4-{3-[(2-oxo-1,2-dihydro-3H-indol-3-yliden)amino]phenoxy}phenyl)imino]-1H-indol-2-one as a novel Schiff base
Molbank 2005, 2005(3), M429; https://doi.org/10.3390/M429
Received: 5 July 2004 / Accepted: 15 July 2004 / Published: 1 August 2005
Cited by 1 | PDF Full-text (137 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Isatin is an endogenous compound isolated in 1988 [1] and reported to possess a wide range of central nervous system activities [2,3].[...] Full article
Open AccessShort Note N-{(2Z)-4-[4-(3-chlorophenyl)piperazin-1-yl]but-2-enyl}-1,8-naphthalimide
Molbank 2005, 2005(3), M430; https://doi.org/10.3390/M430
Received: 14 July 2004 / Accepted: 15 July 2004 / Published: 1 August 2005
PDF Full-text (129 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
In continuation of our interest on synthesis and properties of arylpiperazine derivatives investigated as a serotonin receptors ligands [1,2,3], herein we presented one-pot synthesis of N-{(2Z)-4-[4-(3-chlorophenyl)piperazin-1-yl]but-2-enyl}-1,8-naphthalimide (4).[...] Full article
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