An unusual transformation of 2-(5-aryl-2-oxo-3H-pyrrol-3-ylidene)malononitriles occurring through a nucleophilic addition to the C5 atom of the heterocycle is described. The observed process is reversible and characterized by a contrasting color...
SummaryAn efficient diastereoselective approach for the synthesis of functionalized 3,4-dihydro-2H-pyran-4-carboxamides with variable frame was developed based on the reaction of available 4-oxoalkane-1,1,2,2-tetracarbonitriles (adducts of TCNE and ketones) with aldehydes in an acidic media. An unusual process of quasi hydrolysis of the cyano group was observed in the course of the described regio- and diastereoselective transformation.
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