Title of article :
Expedient synthesis of a highly substituted tropolone via a 3-oxidopyrylium [5+2] cycloaddition reaction
Author/Authors :
Baldwin، نويسنده , , Jack E. and Mayweg، نويسنده , , Alexander V.W. and Pritchard، نويسنده , , Gareth J. and Adlington، نويسنده , , Robert M.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2003
Pages :
3
From page :
4543
To page :
4545
Abstract :
An expedient ten-step synthesis of a substituted tropolone is described. The synthesis involves a 3-oxidopyrylium [5+2] cycloaddition reaction with acrylonitrile as the key step, affording a highly functionalized [3.2.1]-bicycle 10 as a single regioisomer. The nitrile substituent of the reduced cycloadduct 12 permits efficient ether-bridge cleavage and tropolone 15 is obtained after a final bis-oxidation procedure. The pyranulose acetate cycloaddition precursor was derived from 3-methyl-2-furoate.
Journal title :
Tetrahedron Letters
Serial Year :
2003
Journal title :
Tetrahedron Letters
Record number :
1662505
Link To Document :
بازگشت