Title of article :
An efficient synthesis of oosporein
Author/Authors :
Love، نويسنده , , Brian E. and Bonner-Stewart، نويسنده , , Jeffrey and Forrest، نويسنده , , Lori A.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Abstract :
Fungal metabolite oosporein was prepared in four steps and 24% overall yield starting from 2,5-dimethoxytoluene. It was demonstrated that treatment of phoenicin with pyrrolidine and copper(II) acetate led to oosporein, whereas similar treatment of the isomeric ‘isophoenicin’ produced a benzofuran diquinone. No chromatography was required during any step of the synthesis.
Keywords :
Thiele-Winter acetoxylation , Oosporein , total synthesis , Diquinone
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters