Ontology type: schema:ScholarlyArticle
2012-12
AUTHORSA. I. Vas’kevich, N. M. Tsyzoryk, V. I. Staninets, E. B. Rusanov, M. V. Vovk
ABSTRACTN-Aryl-4-phenylbut-3-enamides reacted with arenesulfenyl chlorides in chloroform to give N,4-diaryl-3-arylsulfanyl-4-chlorobutanamides, whereas in acetic acid in the presence of lithium perchlorate N-[4-arylsulfanyl-5-phenyltetrahydrofuran-2-ylidene]arenaminium perchlorates were obtained. Reactions of arenesulfenyl chlorides with N,4-diarylbut-3-enamides having strong electron-donating groups in positions 3 and 4 of the N-aryl substituent afforded 5-aryl-4-arylsulfanyl-2,3,4,5-tetrahydro-1H-1-benzazepin-2-ones.
PAGES1536-1543
http://scigraph.springernature.com/pub.10.1134/s107042801212007x
DOIhttp://dx.doi.org/10.1134/s107042801212007x
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