Next Issue
Volume 2011, December
Previous Issue
Volume 2011, June

Table of Contents

Molbank, Volume 2011, Issue 3 (September 2011) – 9 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
4-{[(4-Methylphenyl)imino]methyl}-3-hydroxyphenyl 4-(Hexadecanoyloxy)benzoate
Molbank 2011, 2011(3), M738; https://doi.org/10.3390/M738 - 23 Sep 2011
Viewed by 2249
Abstract
A new Schiff base, 4-{[(4-methylphenyl)imino]methyl}-3-hydroxyphenyl 4-(hexadecanoyloxy)benzoate was synthesized and its IR, 1H NMR, 13C NMR and MS spectroscopic data are presented. Full article
Show Figures

Graphical abstract

Open AccessShort Note
2-tert-Butyl-5,6,7,8,9,10-hexahydrocyclohepta[b]indole
Molbank 2011, 2011(3), M737; https://doi.org/10.3390/M737 - 21 Sep 2011
Cited by 5 | Viewed by 2695
Abstract
2-tert-Butyl-5,6,7,8,9,10-hexahydrocyclohepta[b]indole was synthesized by reaction of cycloheptanone and (4-tert-butylphenyl)hydrazine hydrochloride in the presence of sodium acetate and sulfuric acid in glacial acetic acid via Fischer indole synthesis. Full article
Show Figures

Graphical abstract

Open AccessShort Note
Anthracen-9-ylmethylene-(3,4-dimethylisoxazol-5-yl)amine
Molbank 2011, 2011(3), M736; https://doi.org/10.3390/M736 - 13 Sep 2011
Viewed by 2566
Abstract
The title compound, anthracen-9-ylmethylene-(3,4-dimethylisoxazol-5-yl)amine (3), was synthesized in high yield by reaction of anthracene-9-carbaldehyde and 5-amino-3,4-dimethyl­isoxazole in ethanol. The structure of this new compound was confirmed by elemental analysis, IR, 1H NMR, 13C NMR and GC-MS spectral analysis. Full article
Show Figures

Graphical abstract

Open AccessShort Note
4-({[4-(Methylthio)phenyl]methylene}amino)phenyl Dodecanoate
Molbank 2011, 2011(3), M735; https://doi.org/10.3390/M735 - 09 Sep 2011
Viewed by 2546
Abstract
A new Schiff base ester, 4-({[4-(methylthio)phenyl]methylene}amino)phenyl dodecanoate was synthesized and its IR, 1H NMR, 13C NMR and EI-MS spectroscopic data are presented. Full article
Show Figures

Graphical abstract

Open AccessShort Note
3-Chloro-N'-(2-hydroxy-4-pentadecylbenzylidene) benzothiophene-2-carbohydrazide
Molbank 2011, 2011(3), M734; https://doi.org/10.3390/M734 - 01 Sep 2011
Cited by 1 | Viewed by 2708
Abstract
The title compound, 3-chloro-N'-(2-hydroxy-4-pentadecylbenzylidene)­benzo[b]thiophene-2-carbohydrazide has been synthesized by reaction of 2-hydroxy-4-pentadecylbenzaldehyde with 3-chloro-1-benzo[b]thiophene-2-carboxylic acid hydrazide in the presence of acetic acid in ethanol. The structure of this new compound was confirmed by elemental analysis, IR, 1H-NMR, 13C-NMR and mass spectral analysis. Full article
Show Figures

Graphical abstract

Open AccessShort Note
5-[(5-Chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)methylene]-2-(4-nitrobenzoyl)-3-phenyl-2,5-dihydro-1,2,4-triazin-6(1H)-one
Molbank 2011, 2011(3), M733; https://doi.org/10.3390/M733 - 11 Aug 2011
Viewed by 2544
Abstract
A novel 1,2,4-triazin-6-one derivative (2) was synthesized by the reaction of the oxazolone derivative 1 with 4-nitrobenzoic acid hydrazide in the presence of sodium acetate and glacial acetic acid. The title compound 2 was characterized on basis of IR, 1H-NMR, [...] Read more.
A novel 1,2,4-triazin-6-one derivative (2) was synthesized by the reaction of the oxazolone derivative 1 with 4-nitrobenzoic acid hydrazide in the presence of sodium acetate and glacial acetic acid. The title compound 2 was characterized on basis of IR, 1H-NMR, 13C-NMR and mass spectral data. Full article
Show Figures

Graphical abstract

Open AccessShort Note
4-{[(4-Iodophenyl)imino]methyl}phenyl Octadecanoate
Molbank 2011, 2011(3), M732; https://doi.org/10.3390/M732 - 10 Aug 2011
Viewed by 2707
Abstract
A new Schiff base ester, 4-{[(4-iodophenyl)imino]methyl}phenyl octadecanoate was synthesized and its IR, 1H NMR, 13C NMR and EI-MS spectroscopic data are presented. Full article
Show Figures

Graphical abstract

Open AccessShort Note
N-[1-(1H-Benzimidazol-2-yl)-2-(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)vinyl]benzamide
Molbank 2011, 2011(3), M731; https://doi.org/10.3390/M731 - 25 Jul 2011
Viewed by 2615
Abstract
A novel benzimidazole derivative (2) was synthesized by hydrolyzing 4-[(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)methylene]-2-phenyloxazol-5(4H)-one (1), the azlactone precursor in an acidic medium and treating the product with o-phenylenediamine (OPDA) in situ. The structure of the title compound (2 [...] Read more.
A novel benzimidazole derivative (2) was synthesized by hydrolyzing 4-[(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)methylene]-2-phenyloxazol-5(4H)-one (1), the azlactone precursor in an acidic medium and treating the product with o-phenylenediamine (OPDA) in situ. The structure of the title compound (2) was established on basis of FT-IR, 1H-NMR, 13C-NMR and mass spectral data. Full article
Show Figures

Graphical abstract

Open AccessShort Note
2,3-Diaminophenazine
Molbank 2011, 2011(3), M730; https://doi.org/10.3390/M730 - 18 Jul 2011
Cited by 14 | Viewed by 4045
Abstract
Herein, we synthesized 2,3-diaminophenazine (DAP) from o-phenylenediamine (OP) using fungal laccase as a biocatalyst. The conversion ratio of OP monomer was 85% and the yield of the final purified product, DAP, was 63%. The structure of the main product, DAP, was confirmed by [...] Read more.
Herein, we synthesized 2,3-diaminophenazine (DAP) from o-phenylenediamine (OP) using fungal laccase as a biocatalyst. The conversion ratio of OP monomer was 85% and the yield of the final purified product, DAP, was 63%. The structure of the main product, DAP, was confirmed by using several spectroscopy techniques (UV-VIS, IR, 2D-NMR, and MS). Full article
Show Figures

Graphical abstract

Previous Issue
Back to TopTop