Proton NMR analysis of plasma from renal failure patients: Evaluation of sample preparation and spectral-editing methods

1990 ◽  
Vol 8 (8-12) ◽  
pp. 955-958 ◽  
Author(s):  
E. Holmes ◽  
P.J.D. Foxall ◽  
J.K. Nicholson
1994 ◽  
Vol 35 (11) ◽  
pp. 1925-1931
Author(s):  
R K Adosraku ◽  
G T Choi ◽  
V Constantinou-Kokotos ◽  
M M Anderson ◽  
W A Gibbons

1978 ◽  
Vol 56 (6) ◽  
pp. 789-793 ◽  
Author(s):  
Donald C. Wigfield ◽  
Steve Feiner

The stereoisomers of 2-methyltetrahydropyran-4-ol have been separated and identified by carbon-13 and proton nmr analysis of the trideuteriomethyl-2,6,6-trideuterio analogue. Stereoisomeric product ratios of reduction of 2-methyltetrahydropyran-4-one (1) by NaBH4, KBH4, L-Selectride, K-Selectride, and LiBH(nBu)3 have been determined and compared with reductions of 3-methylcyclohexanone. Product ratios in the reduction of the two substrates by the borohydride reducing agents are similar but are quite different in the reduction by the Selectride reducing agents, 1 being reduced by Selectride to give 73% equatorialalcohol. Two possible mechanisms of reduction of 1 are proposed, involving intramolecular assistance by the cyclic ether oxygen.


2015 ◽  
Vol 11 (2) ◽  
pp. 379-383 ◽  
Author(s):  
C. Airoldi ◽  
F. Tripodi ◽  
C. Guzzi ◽  
R. Nicastro ◽  
P. Coccetti

We present a rapid and reproducible protocol for intracellular metabolite extraction from yeast cells analyzed by1H-NMR spectroscopy.


2006 ◽  
Vol 12 (6) ◽  
pp. 705-710 ◽  
Author(s):  
Heide L Kirschenlohr ◽  
Julian L Griffin ◽  
Sarah C Clarke ◽  
Ranyl Rhydwen ◽  
Andrew A Grace ◽  
...  

1983 ◽  
Vol 105 (4) ◽  
pp. 733-735 ◽  
Author(s):  
Clifford J. Unkefer ◽  
Robert E. London ◽  
Thomas W. Whaley ◽  
Guido H. Daub
Keyword(s):  

1983 ◽  
Vol 105 (18) ◽  
pp. 5945-5946 ◽  
Author(s):  
David G. Reid ◽  
David M. Doddrell ◽  
Keith R. Fox ◽  
Stephen A. Salisbury ◽  
Dudley H. Williams

Synlett ◽  
2017 ◽  
Vol 28 (18) ◽  
pp. 2449-2452
Author(s):  
Scott Sieburth ◽  
Yingjian Bo

A rapid and extremely simple method for silyl anion analysis is presented. The progress of silyllithium reagent preparation can be determined by quenching an aliquot with neat chloro(trimethyl)silane, evaporation, dilution with CDCl3, and direct proton NMR analysis. This procedure is fast, simple, and allows for identification and relative quantification of the starting reagent, intermediates, and the silyllithium product.


2011 ◽  
Vol 4 (1) ◽  
pp. 57-69
Author(s):  
Iago Pinal-Fernandez ◽  
Manuel Martin-Pastor ◽  
Pedro Ferro-Gallego ◽  
Lourdes Dominguez-Gerpe

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