20842-95-9Relevant academic research and scientific papers
Reaction of arynes with vinylogous amides: Nucleophilic addition to the ortho-quinodimethide intermediate
Li, Ran,Wang, Xuemei,Wei, Zhibin,Wu, Chunrui,Shi, Feng
supporting information, p. 4366 - 4369 (2013/09/24)
The reaction of arynes with vinylogous amides containing no free N-H bonds proceeds in a [2 + 2] cycloaddition fashion at ambient temperature. The electronic properties of the vinylogous amides allow for the cycloadducts undergoing a facile ring-opening p
Electroreduction of Organic Compounds, 1. - Condensation Reactions of Acetonitrile with the Aid of Electrogenerated Bases
Kistenbruegger, Lothar,Mischke, Peter,Voss, Juergen,Wiegand, Gabriele
, p. 461 - 471 (2007/10/02)
Electrochemical reduction of alkyl benzoates in dry acetonitrile yields benzoylacetonitrile (2).Methyl 3-cyano-2-hydroxy-2-phenylpropionate (7) is obtained from methyl phenylglyoxalate (5) under the same conditions. - Analogously β-dialkylaminocinnamonitriles 9 can be obtained from N,N-dialkylthiobenzamides 8.N,N-Dimethylbenzamide (10) yields β-dimethylamino-cinnammonitrile (9a) on electroreduction in the presence of azobenzene as a probase by catalytical generation of acetonitrile anions.
