Reactions of aroylhydrazines with nitrosulfodienes of the 2-benzylidene-3-methyl-4-nitro-3-thiolene-1,1-dioxide series

被引:0
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作者
L. V. Lapshina
A. V. Serebryannikova
I. E. Efremova
A. D. Perkhunova
S. V. Bortnikov
V. M. Berestovitskaya
机构
[1] Herzen State Pedagogical University of Russia,
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nitrosulfolene; nitrosulfodiene; aroylhydrazine; aza-Michael reaction;
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摘要
Reactions of s-trans-nitrosulfodienes of the 2-benzylidene-3-methyl-4-nitro-3-thiolene-1,1-dioxide series with aroylhydrazines occur as nucleophilic 1,4-addition to give the aza-Michael adducts. Activity of the studied substrates depends on the nature of the substituents in the benzene ring of benzylidene fragment. Previously unexplored representatives of the 2-benzylidene-3-methyl-4-nitro-3-thiolene-1,1-dioxides have been synthesized.
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页码:1519 / 1523
页数:4
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