Understanding the radical mechanism of lipoxygenases using 31P NMR spin trapping

2011 ◽  
Vol 19 (9) ◽  
pp. 3022-3028 ◽  
Author(s):  
Luca Zoia ◽  
Raffaella Perazzini ◽  
Claudia Crestini ◽  
Dimitris S. Argyropoulos
2000 ◽  
Vol 65 (17) ◽  
pp. 5098-5103 ◽  
Author(s):  
Luis Julià ◽  
M. Pilar Bosch ◽  
Sergio Rodriguez ◽  
Angel Guerrero

2009 ◽  
Vol 23 (6) ◽  
pp. 505-512 ◽  
Author(s):  
Luca Zoia ◽  
Dimitris S. Argyropoulos
Keyword(s):  
31P Nmr ◽  

1980 ◽  
Vol 58 (22) ◽  
pp. 2386-2393 ◽  
Author(s):  
Dominic W. K. Yeung ◽  
John Warkentin

Alkylazodiphenylmethanols (C6H5)2C(OH)N = NR, (R = CH(CH3)2, CH2CH3, CH3), when decomposed in the presence of olefinic substrates or in the presence of azobenzene, hydroalkylate those substrates. Addition of R and H across the double bond of an unsymmetric alkene occurs with the regiochemistry expected for a radical mechanism, in which the group R adds first. Radical intermediates from decomposition of alkylazodiphenylmethanols have been demonstrated earlier with spin trapping experiments. The fact that addition of phenol can enhance the yield of hydroalkylation product suggests that the process is a radical chain reaction, with chain carrying steps consisting of the reactions:[Formula: see text]One deuterioalkylation and some yield-optimizing experiments are also reported.


1983 ◽  
Vol 80 ◽  
pp. 831-832 ◽  
Author(s):  
A.M. Avedikian ◽  
D. Besserre ◽  
M. Delepierre

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