70134-01-9Relevant academic research and scientific papers
Iminovinyl Carboxylates - O-Acyl Products of Enaminones with Acyl Chlorides
Walter, Wolfgang,Saha, Chantu Ranjan
, p. 1095 - 1100 (2007/10/02)
On reaction of cyclic, secondary enaminones 6 with pivaloyl or benzoyl chloride the hitherto unknown iminovinyl carboxylates 7 are obtained; with acetyl chloride the O,N-diacetyl compounds 8 are formed.The esters 7 are present as E,Z isomers.
ALKYLIERUNGSREAKTIONEN AN THIOAMIDEN, VII. ALKYLIERUNG VON VINYLOGEN THIOAMIDEN UND STEREOCHEMIE DER ALKYLIERUNGSPRODUKTE
Walter, Wolfgang,Saha, Chantu Ranjan
, p. 367 - 385 (2007/10/02)
On reacting the cyclic enaminothiones 1 with alkyl halides and pulverized sodiumhydroxide in acetone, the hitherto difficultly accessible thioenimines 8 are obtained in fair yield.They show Z-E isomerism at the substituted imino group.The isomers were ass
α,β-UNSATURATED THIO COMPOUNDS. XIII.* HYDROTHIOLYSIS OF β-HETERO-SUBSTITUTED α,β-UNSATURATED IMMONIUM SALTS AT THE C=N(+) BOND - A GENERAL APPROACH TO THE SYNTHESIS OF FUNCTIONALLY SUBSTITUTED THIOKETONES
Usov, V. A.,Timokhina, L. V.,Zhagun, V. A.,Sidorkin, V. F.,Voronkov, M. G.
, p. 1623 - 1628 (2007/10/02)
The hydrothiolysis of immonium salts containing the Y-C=C-C=N(+) group takes place at the C=N(+) bond and not at the C-Y bond.This is consistent with the results from quantum-chemical calculations.On this basis a general approach was formulated to the synthesis of new types of organic sulfur compounds, i.e. β-alkoxy-, β-alkylthio-, and β-halogen-substituted α,β-unsaturated thioketones of the Y-C=C-C=S (Y=RO, RS, Hlg) type.
