Epoxidation of olefins by cytochrome P-450 model compounds: kinetics and stereochemistry of oxygen atom transfer and origin of shape selectivity

1985 ◽  
Vol 107 (7) ◽  
pp. 2000-2005 ◽  
Author(s):  
James P. Collman ◽  
John I. Brauman ◽  
Bernard Meunier ◽  
Teruyuki Hayashi ◽  
Thomas Kodadek ◽  
...  
1984 ◽  
Vol 81 (10) ◽  
pp. 3245-3248 ◽  
Author(s):  
J. P. Collman ◽  
J. I. Brauman ◽  
B. Meunier ◽  
S. A. Raybuck ◽  
T. Kodadek

2010 ◽  
Vol 49 (19) ◽  
pp. 8914-8921 ◽  
Author(s):  
Nadia C. Mösch-Zanetti ◽  
Dietmar Wurm ◽  
Manuel Volpe ◽  
Ganna Lyashenko ◽  
Bastian Harum ◽  
...  

2007 ◽  
Vol 11 (02) ◽  
pp. 95-99 ◽  
Author(s):  
Rezvan Babakhani ◽  
Farzad Bahadoran ◽  
Nasser Safari

Two complexes of ruthenium(II) carbonyl tetraphenyl- and tetramesytilporphyrins were used as catalysts for epoxidation of olefins using metachloroperbenzoic acid and iodosylbenzene, as oxidants. Better results were obtained with the ( TPP ) RuCO catalyst in the presence of metachloroperbenzoic acid; however, iodosylbenzene showed higher yields than metachloroperbenzoic acid for some aromatic olefins. The effect of imidazole axial base was also investigated. Two different pathways are proposed based on these two oxygen atom transfer agents.


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