Unique properties of the 11-cis and 11,11′-di-cis isomers of β-carotene as revealed by electronic absorption, resonance Raman and 1H and 13C NMR spectroscopy and by HPLC analysis of their thermal isomerization

1997 ◽  
pp. 2699-2710 ◽  
Author(s):  
Ying Hu ◽  
Hideki Hashimoto ◽  
Gérard Moine ◽  
Urs Hengartner ◽  
Yasushi Koyama
Keyword(s):  
Nmr Spectroscopy ◽  
Electronic Absorption ◽  
13C Nmr ◽  
Hplc Analysis ◽  
Resonance Raman ◽  
13C Nmr Spectroscopy ◽  
Thermal Isomerization ◽  
1H And 13C Nmr ◽  
Absorption Resonance ◽  
Β Carotene

scholarly journals Synthesis and characterization of tris[butyl-(1-methyl-3phenyl-propyl)-dithiocarbamato]cobalt(III) seskvitoluen

2002 ◽  
Vol 67 (2) ◽  
pp. 123-126 ◽  
Author(s):  
Goran Kaludjerovic ◽  
Vesna Djinovic ◽  
Srecko Trifunovic ◽  
Ismet Hodzic ◽  
Tibor Sabo
Keyword(s):  
Nmr Spectroscopy ◽  
Electronic Absorption ◽  
Elemental Analysis ◽  
13C Nmr ◽  
Sodium Salt ◽  
13C Nmr Spectroscopy ◽  
Bidentate Ligand ◽  
Synthesis And Characterization ◽  
1H And 13C Nmr

Anew bidentate ligand butyl-(1-methyl-3-phenyl-propyl)-dithiocarbamate (bm?pdtc) was prepared, as the sodium salt. In the reaction of hexaaminecobalt(III) chloride with Nabm?pdtc, the corresponding tris[butyl-(1-methyl-3-phenyl-propyl)-dithiocarbamato]cobalt(III) [Co(bm?pdtc)3]?complex was prepared. The complex was characterized by elemental analysis, infrared, electronic absorption, 1H and 13C-NMR spectroscopy.

scholarly journals (2S,3R,6R)-2-[(R)-1-Hydroxyallyl]-4,4-dimethoxy-6-methyltetrahydro-2H-pyran-3-ol

Molbank ◽  
10.3390/m1140 ◽  
2020 ◽  
Vol 2020 (2) ◽  
pp. M1140
Author(s):  
Jack Bennett ◽  
Paul Murphy
Keyword(s):  
Mass Spectrometry ◽  
Nmr Spectroscopy ◽  
Ir Spectroscopy ◽  
13C Nmr ◽  
Conjugate Addition ◽  
13C Nmr Spectroscopy ◽  
One Pot ◽  
1H And 13C Nmr ◽  
Esi Mass Spectrometry ◽  
The One

(2S,3R,6R)-2-[(R)-1-Hydroxyallyl]-4,4-dimethoxy-6-methyltetrahydro-2H-pyran-3-ol was isolated in 18% after treating the glucose derived (5R,6S,7R)-5,6,7-tris[(triethylsilyl)oxy]nona-1,8-dien-4-one with (1S)-(+)-10-camphorsulfonic acid (CSA). The one-pot formation of the title compound involved triethylsilyl (TES) removal, alkene isomerization, intramolecular conjugate addition and ketal formation. The compound was characterized by 1H and 13C NMR spectroscopy, ESI mass spectrometry and IR spectroscopy. NMR spectroscopy was used to establish the product structure, including the conformation of its tetrahydropyran ring.

scholarly journals NEW PHARMACOLOGICALLY ACTIVE COMPOUNDS BASED ON 5-HYDROXY-7-METHOXY-2-PHENYLCHROMAN-4-ONE

2021 ◽  
Vol 3 ◽  
pp. 119-127
Author(s):  
G.M. Baisarov ◽  
◽  
S.M. Adekenov ◽  
Keyword(s):  
Nmr Spectroscopy ◽  
13C Nmr ◽  
Potassium Carbonate ◽  
13C Nmr Spectroscopy ◽  
1H And 13C Nmr ◽  
Pharmacologically Active ◽  
Pharmacologically Active Compounds ◽  
First Time

The reaction of 5-hydroxy-7-methoxy-2-phenylchroman-4-one with dibromoalkanes in acetone in the presence of potassium carbonate proceeds according to the Michael’s retro-reaction O-alkylation and leads to the formation of the corresponding 2-(bromo-alkoxy) chalcones. The structure of the synthesized compounds was confirmed by IR-, 1H- and 13C-NMR spectroscopy. The cytotoxic, hepatoprotective and anti-inflammatory effects of chalcone derivatives (2-3) were studied for the first time in vitro and in vivo.

A structural study of silicon-based interpenetrating polymer networks by solid state 1H and 13C NMR spectroscopy

2002 ◽  
Vol 602-603 ◽  
pp. 321-333 ◽  
Author(s):  
Masatoshi Kobayashi ◽  
Shigeki Kuroki ◽  
Isao Ando ◽  
Kazuo Yamauchi ◽  
Hideaki Kimura ◽  
...  
Keyword(s):  
Solid State ◽  
Nmr Spectroscopy ◽  
Structural Study ◽  
13C Nmr ◽  
Polymer Networks ◽  
13C Nmr Spectroscopy ◽  
Interpenetrating Polymer Networks ◽  
1H And 13C Nmr ◽  
Silicon Based
Sign in / Sign up

Export Citation Format

Share Document