Title of article
Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans via a two-step sequential Michael-Evans aldol cyclization strategy: total synthesis of (+)-magnolone
Author/Authors
Pandey، نويسنده , , Ganesh and Luckorse، نويسنده , , Srikanth and Budakoti، نويسنده , , Asha and Puranik، نويسنده , , Vedavati G.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
4
From page
2975
To page
2978
Abstract
Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans is described employing a two-step Michael-Evans aldol cyclization strategy. The approach is successfully applied for the total synthesis of furano lignan natural product (+)-magnolone.
Keywords
Tetrahydrofuran , HWE reaction , Magnolone , Michael-Evans aldol reaction , Lignans
Journal title
Tetrahedron Letters
Serial Year
2010
Journal title
Tetrahedron Letters
Record number
1872246
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