Title of article
Diastereoselective construction of substituted tetrahydropyrans using an intramolecular oxy-Michael strategy
Author/Authors
Yakushiji، نويسنده , , Fumika and Maddaluno، نويسنده , , Jacques and Yoshida، نويسنده , , Masahiro and Shishido، نويسنده , , Kozo، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2009
Pages
3
From page
1504
To page
1506
Abstract
The highly diastereoselective construction of substituted tetrahydropyrans, a common core segment (C3–C10) of the thiomarinols and the pseudomonic acid antibiotics, has been accomplished using the intramolecular oxy-Michael reaction under both basic and high-pressure conditions followed by regio- and stereoselective epoxide opening with acetylide.
Journal title
Tetrahedron Letters
Serial Year
2009
Journal title
Tetrahedron Letters
Record number
1863017
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