| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281241 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A thiophile-promoted one-pot synthesis of trisubstituted 1,3,5-triazines starting from isothiocyanates, N,N-diethylamidines, and carbamidines has been studied. The reaction proceeds through the formation of intermediary amidinothioureas, which react with carbamidines in the presence of mercury(II) chloride to generate the desired 1,3,5-triazines in good to moderate yields (40-70%).
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jitendra C. Kaila, Arshi B. Baraiya, Amit N. Pandya, Hitesh B. Jalani, V. Sudarsanam, Kamala K. Vasu,