Title of article :
Synthesis of substituted 2,3-dihydrobenzofuran in a process involving a facile acyl migration
Author/Authors :
Li، نويسنده , , Wen-Sen and Guo، نويسنده , , Zhenrong and Thornton، نويسنده , , John and Katipally، نويسنده , , Kishta and Polniaszek، نويسنده , , Richard and Thottathil، نويسنده , , John and Vu، نويسنده , , Truc and Wong، نويسنده , , Michael، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
3
From page :
1923
To page :
1925
Abstract :
Reduction of 2,6-diacetoxy-2′-bromoacetophenone (10) with NaBH4 led to 3,4-diacetoxydihydrobenzofuran (12) in a process involving acyl migration followed by cyclization. Subsequent hydrogenolysis gave 4-acetoxydihydrobenzofuran which, upon saponification, afforded 4-hydroxydihydrobenzofuran (8) in good yield. This approach is shown to be a general method for preparation of substituted dihydrobenzofurans.
Journal title :
Tetrahedron Letters
Serial Year :
2002
Journal title :
Tetrahedron Letters
Record number :
1650429
Link To Document :
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