Title of article
Rapid access to the synthesis of polysubstituted δ-lactones via tandem stereoselective conjugate addition/α-alkylation of unsaturated 7,3-lactone-α-d-xylofuranose derivative
Author/Authors
Ramيrez، نويسنده , , Elsie and Quintero، نويسنده , , Leticia and Meza-Leَn، نويسنده , , Rosa L. and Sosa-Rivadeneyra، نويسنده , , Martha and Cruz-Gregorio، نويسنده , , Silvano and Sartillo-Piscil، نويسنده , , Fernando، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
4
From page
5751
To page
5754
Abstract
α-d-xylo-7,3-Unsaturated lactone, a versatile chiral building block, undergoes Cu-catalyzed conjugated addition with high yield and stereoselectivity. When the conjugated reaction is quenched with a suitable alkyl halide, a tandem stereoselective conjugated/α-alkylation reaction is achieved. Further, selective hydrolysis of the 1,2-O-isopropylidene moiety followed by oxidative cleavage and reduction reaction, afforded the title compounds.
Keywords
conjugate addition , stereoselectivity , ?-Lactones , tandem , carbohydrates
Journal title
Tetrahedron Letters
Serial Year
2013
Journal title
Tetrahedron Letters
Record number
1886346
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