Relationship between the gas chromatographic behaviour and the molecular structure of hydrocarbon samples and various stationary phases

1980 ◽  
Vol 13 (2) ◽  
pp. 93-100 ◽  
Author(s):  
V. M. Nabivach ◽  
A. V. Kirilenko
1977 ◽  
Vol 161 (2) ◽  
pp. 233-237 ◽  
Author(s):  
R J Yon

Six out of seven enzymes tested (four of them nicotinamide nucleotide-dependent dehydrogenases) showed differences in chromatographic behaviour in the presence and absence of their biospecific ligands, when chromatographed on immobilized amphipathic ampholytes (‘imphilytes’) as stationary phases. Some enzymes were adsorbed more tightly, others less tightly, in the presence of ligands. These results have implications for enzyme purification in general, and for some types of affinity chromatography in particular.


1968 ◽  
Vol 42 (1) ◽  
pp. 45-54 ◽  
Author(s):  
H. J. van der MOLEN ◽  
D. GROEN ◽  
F. F. G. ROMMERTS ◽  
J. H. VAN DER MAAS

SUMMARY 20α-Hydroxy-5β-pregnan-3-one was isolated from the extracts of enzyme or acid-hydrolysed pregnancy urine using various chromatographic procedures including gas chromatography Identification of the steroid was based upon: (1) behaviour of the free and acetylated compound, and of the products, following stereospecific enzymatic oxidations, during gas chromatography on different stationary phases, and (2) infrared spectrometry of the compound collected after gas chromatography. The gas-chromatographic behaviour of the isomers of 3-hydroxypregnan-20-one, 20-hydroxypregnan3-one and pregnane-3,20-diol and their acetates is reported.


2006 ◽  
Vol 1128 (1-2) ◽  
pp. 105-113 ◽  
Author(s):  
Dao T.-T. Nguyen ◽  
Davy Guillarme ◽  
Serge Rudaz ◽  
Jean-Luc Veuthey

2011 ◽  
Vol 1218 (35) ◽  
pp. 5939-5963 ◽  
Author(s):  
Raluca-Ioana Chirita ◽  
Caroline West ◽  
Sandrine Zubrzycki ◽  
Adriana-Luminita Finaru ◽  
Claire Elfakir

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