Powerful Approach to Heterocyclic Skeletal Diversity by Sequential Three-Component Reaction of Amines, Isothiocyanates, and 1,2-Diaza-1,3-dienes

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• 作者：Orazio A. Attanasi ; Silvia Bartoccini ; Gianfranco Favi ; Gianluca Giorgi ; Francesca Romana Perrulli ; Stefania Santeusanio
• 刊名：The Journal of Organic Chemistry
• 出版年：2012
• 出版时间：January 20, 2012
• 年：2012
• 卷：77
• 期：2
• 页码：1161-1167
• 全文大小：278K
• 年卷期：v.77,no.2(January 20, 2012)
• ISSN：1520-6904

文摘

By highly efficient, one-pot, three-component reactions, combining one set of 1,2-diaza-1,3-dienes (DDs), primary amines, and isothiocyanates in a different sequential order of addition, heterocyclic skeletal diversity can be achieved. The key feature discriminating the different heterocyclic core formation is the availability of the N or S heteronucleophile to give the first Michael addition step affording regioselective substituted 2-thiohydantoins or 2-iminothiazolidinones. The hydrazone or enehydrazino side chain at the 5-position of both heterocycles represents a valuable functionality to reach novel 5-hydroxyethylidene derivatives difficult to obtain by other methods.