Title of article
Synthesis of 3,4-disubstituted 2,5-dihydrofurans starting from the Baylis–Hillman adducts via consecutive radical cyclization, halolactonization, and decarboxylation strategy
Author/Authors
Gowrisankar، نويسنده , , Saravanan and Lee، نويسنده , , Ka Young and Kim، نويسنده , , Jae Nyoung، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
5
From page
4859
To page
4863
Abstract
A facile synthetic method of 3,4-disubstituted 2,5-dihydrofurans and 2,5-dihydropyrroles starting from the Baylis–Hillman adducts was developed. The 2,5-dihydrofuran skeleton was constructed via the consecutive radical cyclization, hydrolysis, halolactonization, and spontaneous decarboxylation strategy starting from the modified Baylis–Hillman adducts.
Keywords
Baylis–Hillman adducts , 2 , 5-dihydrofurans , radical cyclization , Halolactonization
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1846159
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