scholarly journals Detection of [1,6-13C2]-glucose metabolism in rat brain by in vivo1H-[13C]-NMR spectroscopy

2002 ◽  
Vol 49 (1) ◽  
pp. 37-46 ◽  
Author(s):  
Robin A. de Graaf ◽  
Peter B. Brown ◽  
Graeme F. Mason ◽  
Douglas L. Rothman ◽  
Kevin L. Behar
Keyword(s):  
Nmr Spectroscopy ◽  
Glucose Metabolism ◽  
Rat Brain ◽  
13C Nmr ◽  
13C Nmr Spectroscopy

scholarly journals Determination of Oxidative Glucose Metabolism In Vivo in the Young Rat Brain Using Localized Direct-Detected 13C NMR Spectroscopy

2011 ◽  
Vol 36 (11) ◽  
pp. 1962-1968 ◽  
Author(s):  
Kathleen Ennis ◽  
Dinesh Kumar Deelchand ◽  
Ivan Tkac ◽  
Pierre-Gilles Henry ◽  
Raghavendra Rao
Keyword(s):  
Nmr Spectroscopy ◽  
Glucose Metabolism ◽  
Rat Brain ◽  
13C Nmr ◽  
13C Nmr Spectroscopy ◽  
Young Rat

Cerebral glucose metabolism and the glutamine cycle as detected by in vivo and in vitro 13C NMR spectroscopy

2004 ◽  
Vol 45 (2-3) ◽  
pp. 297-303 ◽  
Author(s):  
Marı́a A Garcı́a-Espinosa ◽  
Tiago B Rodrigues ◽  
Alejandra Sierra ◽  
Marina Benito ◽  
Carla Fonseca ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Glucose Metabolism ◽  
13C Nmr ◽  
13C Nmr Spectroscopy ◽  
Cerebral Glucose Metabolism

scholarly journals In vivoneurochemical profiling of rat brain by1H-[13C] NMR spectroscopy: cerebral energetics and glutamatergic/GABAergic neurotransmission

2010 ◽  
Vol 112 (1) ◽  
pp. 24-33 ◽  
Author(s):  
Pieter van Eijsden ◽  
Kevin L. Behar ◽  
Graeme F. Mason ◽  
Kees P. J. Braun ◽  
Robin A. de Graaf
Keyword(s):  
Nmr Spectroscopy ◽  
Rat Brain ◽  
13C Nmr ◽  
13C Nmr Spectroscopy ◽  
Gabaergic Neurotransmission

scholarly journals Decreased TCA cycle rate in the rat brain after acute 3-NP treatment measured by in vivo1H-{13C} NMR spectroscopy

2002 ◽  
Vol 82 (4) ◽  
pp. 857-866 ◽  
Author(s):  
Pierre-Gilles Henry ◽  
Vincent Lebon ◽  
Françoise Vaufrey ◽  
Emmanuel Brouillet ◽  
Philippe Hantraye ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Rat Brain ◽  
13C Nmr ◽  
Tca Cycle ◽  
13C Nmr Spectroscopy ◽  
Cycle Rate

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.

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