期刊
TETRAHEDRON
卷 145, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2023.133603
关键词
Baylis-Hillman adducts; Piperidine-2,6-dione; Indenone; Tetralone; Friedel-crafts cyclization
A simple and efficient method for synthesizing (E)-5-arylylidene-3-((substituted-ind-2-en-1-one)methyl)-3-aryl piperidine-2,6-diones from Baylis-Hillman acetates is described. This involves bis-alkylation of aryl acetonitriles followed by a facile domino bis-cyclization reaction involving C-C and C-N bond formations.
A simple and efficient synthesis of (E)-5-arylylidene-3-((substituted-ind-2-en-1-one)methyl)-3-aryl piperidine-2,6-diones from Baylis-Hillman acetates via bis-alkylation of aryl acetonitriles followed by facile domino bis- cyclization involving C-C bond and C-N bond formation reactions are described.
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