Hydride Reduction of NAD+Analogues by Isopropyl Alcohol: Kinetics, Deuterium Isotope Effects and Mechanism

2008 ◽  
Vol 73 (13) ◽  
pp. 4763-4770 ◽  
Author(s):  
Yun Lu ◽  
Fengrui Qu ◽  
Brian Moore ◽  
Donald Endicott ◽  
William Kuester





1979 ◽  
Vol 44 (1) ◽  
pp. 110-122 ◽  
Author(s):  
Jiří Velek ◽  
Bohumír Koutek ◽  
Milan Souček

Competitive hydration and isomerisation of the quinone methide I at 25 °C in an aqueous medium in the region of pH 2.4-13.0 was studied spectrophotometrically. The only reaction products in the studied range of pH are 4-hydroxybenzyl alcohol (II) and 4-hydroxystyrene (III). The form of the overall rate equation corresponds to a general acid-base catalysis. The mechanism of both reactions for three markedly separated pH regions is discussed on the basis of kinetic data and solvent deuterium effect.



1984 ◽  
Vol 80 (1) ◽  
pp. 585-587 ◽  
Author(s):  
Roderick E. Wasylishen ◽  
Jan O. Friedrich


2000 ◽  
Vol 122 (51) ◽  
pp. 12878-12879 ◽  
Author(s):  
Parwin Schah-Mohammedi ◽  
Ilja G. Shenderovich ◽  
Carsten Detering ◽  
Hans-Heinrich Limbach ◽  
Peter M. Tolstoy ◽  
...  


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