Published January 1, 2021
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Claisen type Condensation of Methyl Ketones with Carbimidothioates: A New Gateway for the Synthesis of beta-Enaminones
- 1. Univ Mysore, Inst Excellence, Mysuru 570006, India
- 2. Yildiz Tech Univ, Fac Arts & Sci, Dept Chem, TR-34210 Istanbul, Turkey
Description
Carbimidothioates are synthesized by the reaction of Grignard reagents or heteroaryl lithium compounds with arylisothiocyanates followed by treatment with methyl iodide. Further, application of these intermediates in the synthesis of beta-enaminones by their condensation with methyl ketones in the presence of sodium hydride in DMF is reported. This method offers a new gateway for the synthesis of beta-enaminones, which are important building blocks in synthetic organic chemistry.
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