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Synthetic Exploitation of the Ring-Opening of 3,4-Dinitrothiophene. A Novel Access to 1,4-Dialkyl- and 1,4-Diaryl-2,3-dinitro-1,3-butadienes

Academic Article
Publication Date:
1990
abstract:
(E,E)-1,4-Bis(diethylamino)-2,3-dinitro-1,3-butadiene (2a), obtained from the ring-opening of 3,4-dinitrothiophene, reacts with Grignard reagents in THF to give good yields of 1,4-disubstituted ( Et, cy-Hex, Ph ) 2,3-dinitro- 1, 3-butadienes (3a-c) having almost exclusively (E,E) configuration.
Iris type:
01.01 Articolo in rivista
List of contributors:
Stagnaro, Paola
Authors of the University:
STAGNARO PAOLA
Handle:
https://iris.cnr.it/handle/20.500.14243/204911
Published in:
TETRAHEDRON LETTERS
Journal
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http://ac.els-cdn.com/S0040403900977736/1-s2.0-S0040403900977736-main.pdf?_tid=fc73ec8a-ff84-11e2-8720-00000aab0f6c&acdnat=1375895921_bc10f1a13f0753ce53cbf5978b23fd2a
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