Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10596913 | Bioorganic & Medicinal Chemistry Letters | 2005 | 5 Pages |
Abstract
Barbituric acid 1 and related β-dicarbonyl compounds were dialkenylated under the phase-transfer catalyst [e.g., benzyltriethylammonium chloride (BTEAC)] conditions to generate the diallylated products. These diallylated products were subjected to the ring-closing metathesis (RCM) reaction to deliver the corresponding spiro-annulated derivatives.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sambasivarao Kotha, Ashoke Chandra Deb, Ramanatham Vinod Kumar,