| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271666 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
A direct synthesis of 1,3-dienes and 1,3,5-trienes from the reaction of semi-stabilized ylides and a range of saturated and unsaturated aldehydes is reported in water as solvent, employing sodium hydroxide as base. The water-soluble phosphine oxide side product is removed simply by aqueous partitioning of the organic products.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
James McNulty, Priyabrata Das,