Next Issue
Volume 2012, June
Previous Issue
Volume 2012, December

Table of Contents

Molbank, Volume 2012, Issue 1 (March 2012) – 5 articles

  • Issues are regarded as officially published after their release is announced to the table of contents alert mailing list.
  • You may sign up for e-mail alerts to receive table of contents of newly released issues.
  • PDF is the official format for papers published in both, html and pdf forms. To view the papers in pdf format, click on the "PDF Full-text" link, and use the free Adobe Readerexternal link to open them.
Order results
Result details
Select all
Export citation of selected articles as:
Open AccessShort Note
N-(2-Phenoxy-4-(3-phenoxyprop-1-ynyl)phenyl)methane Sulfonamide
Molbank 2012, 2012(1), M751; https://doi.org/10.3390/M751 - 02 Mar 2012
Viewed by 2414
Abstract
The title compound, N-(2-phenoxy-4-(3-phenoxyprop-1-ynyl)phenyl) methanesulfonamide was synthesized in high yield by Sonogashira cross coupling of N-(4-iodo-2-phenoxyphenyl)methanesulfonamide with 3-phenoxyprop-1-yne. The structure of the compound was fully characterized by IR, 1H and 13C NMR, Mass spectra and elemental analysis. Full article
Show Figures

Graphical abstract

Open AccessShort Note
4-[(2-Hydroxy-4-pentadecylbenzylidene)amino]-1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one
Molbank 2012, 2012(1), M750; https://doi.org/10.3390/M750 - 29 Feb 2012
Viewed by 2413
Abstract
Novel 4-[(2-hydroxy-4-pentadecylbenzylidene)amino]-1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one was prepared via condensation of 2-hydroxy-4-pentadecylbenzaldehyde (1) with 4-amino-1,2-dihydro-2,3-dimethyl-1-phenylpyrazol-5-one (2) in ethanol/acetic acid under reflux. The structure of the synthesized compound was assigned on the basis of elemental analysis and spectral data. Full article
Show Figures

Graphical abstract

Open AccessShort Note
Ethyl 3-{2-[(3-Methyl-1H-indol-2-yl)carbonyl]­hydrazinylidene}­butanoate
Molbank 2012, 2012(1), M749; https://doi.org/10.3390/M749 - 07 Feb 2012
Viewed by 2339
Abstract
The title compound, ethyl 3-{2-[(3-methyl-1H-indol-2-yl)carbonyl]hydrazinylidene} butanoate (3), was prepared via reaction of 3-methyl-1H-indole-2-carbohydrazide (1) and ethyl 3-oxo­butanoate (2) under reflux. The structure of the synthesized compound was assigned on the basis of elemental analysis, IR, 1H-NMR, mass spectral and X-ray data. Full article
Show Figures

Graphical abstract

Open AccessShort Note
Nꞌ-{[2-(Piperidin-1-yl)quinolin-3-yl]methylene}pyridine-4-carbohydrazide
Molbank 2012, 2012(1), M748; https://doi.org/10.3390/M748 - 18 Jan 2012
Cited by 1 | Viewed by 2790
Abstract
Nꞌ-{[2-(piperidin-1-yl)quinolin-3-yl]methylene}pyridine-4-carbohydrazide 2 has been synthesized through condensation of 2-(piperidin-1-yl)quinoline-3-carbaldehyde 1 with isonicotinic acid hydrazide (INH) in absolute ethanol. The structure of the title compound 2 was established on the basis of IR, 1H-NMR, 13C-NMR and mass spectral data. Full article
Show Figures

Graphical abstract

Open AccessShort Note
5,11,17,23-Tetra-tert-butyl-25-(2’-pyridylmethylamidocarbonylmethyl)-calix[4]arene
Molbank 2012, 2012(1), M747; https://doi.org/10.3390/M747 - 10 Jan 2012
Viewed by 2504
Abstract
5,11,17,23-tetra-tert-butyl-25-(2’-pyridyl methyl amidocarbonylmethyl)-calix[4]arene (3) has been synthesized in the cône conformation through reaction of the corresponding mono-ester with 2-aminomethylpyridine (picolylamine) and characterised using 1H NMR and MALDI-TOF mass spectral data as well as elemental analyses. Full article
Show Figures

Graphical abstract

Previous Issue
Next Issue
Back to TopTop