Title of article :
The chemical reactivity of a known anti-psoriasis drug. Part 1: Further insights into the products resulting from oxidative cleavage
Author/Authors :
Alan M. Jones، نويسنده , , Magali M. Lorion، نويسنده , , Tomas Lebl، نويسنده , , Alexandra M.Z Slawin، نويسنده , , Douglas Philp، نويسنده , , Nicholas J. Westwood، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2010
Pages :
8
From page :
9667
To page :
9674
Abstract :
The oxidative cleavage of the known anti-psoriasis drug 1 to give 2 has been reported previously. Due to the importance of accessing medium-sized ring containing systems via oxidative cleavage, this reaction has been revisited revealing additional information about the structure of 2. Alternative reaction products were identified when the reaction was carried out in the presence of water. The conversion of 1 to 2 has also been carried out using ruthenium tetroxide. A detailed variable temperature NMR and computational study of the restricted rotation of the N-aryl ring in 2 is presented.
Keywords :
Heterocycle , oxidative fragmentation , Macrocycle , VT NMR analysis , mechanism
Journal title :
Tetrahedron
Serial Year :
2010
Journal title :
Tetrahedron
Record number :
1102751
Link To Document :
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