| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5265107 | Tetrahedron Letters | 2013 | 4 Pages | 
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.
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											Authors
												Elsie RamÃrez, Leticia Quintero, Rosa L. Meza-León, Martha Sosa-Rivadeneyra, Silvano Cruz-Gregorio, Fernando Sartillo-Piscil, 
											