Title of article :
Rearrangements of Trihalomethyl Ketones
Author/Authors :
Samuel Braverman، نويسنده , , Marina Cherkinsky، نويسنده , , E.V.K Suresh Kumar، نويسنده , , Hugo E. Gottlieb، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Pages :
9
From page :
4521
To page :
4529
Abstract :
Trihalomethyl ketones have been prepared and their reactivity under basic conditions was investigated in terms of competition between 1,2- vs. 1,3-elimination and nucleophilic substitution. Favorskii rearrangement was the preferred process, but in those cases where electronic or steric effects were present, nucleophilic substitution became dominant. No evidence of ketene formation was detected. The mechanism of formation of the various rearrangement products is discussed.
Keywords :
?-Elimination , Ketone , Favorskii rearrangement
Journal title :
Tetrahedron
Serial Year :
2000
Journal title :
Tetrahedron
Record number :
1080943
Link To Document :
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