Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5264581 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
A catalyst-free Knoevenagel type synthesis of isatinylidenerhodanines is reported starting from substituted isatins and rhodanines. The reaction proceeds spontaneously at room temperature in dimethyl sulfoxide (DMSO), employing a unique macrocyclic intermediate formed through an intramolecular H-bonding. Various substituted isatinylidenerhodanines could be synthesized in good yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Fengtian Xue, Alexander D. Jr., Geoffrey Heinzl, Kellie Hom,