From 3,4-dinitrothiophene to 1,2-diaryl-4-nitrobenzenes through ( E , E , E )-1,6-diaryl-3-nitro-1,3,5-hexatrienes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
1. Synthetic exploitation of the ring-opening of 3,4-dinitrothiophene, part X. For part IX see Ref. 5.
2. 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
3. Synthetic exploitation of the ring-opening of 3,4-dinitrothiophene. Access to 1,4-disubstituted 2,3-dinitro-1,3-butadienes and 2,3-butanedione dioximes
4. Synthetic exploitation of the ring-opening of 3,4-dinitrothiophene. Access to 1,4-disubstituted 2,3-dinitro-1,3-butadienes and 2,3-diaminobutanes
5. Pyrrolidines, Pyrrolines and Pyrroles from 1,4-Diaryl-2,3-dinitro-1,3-butadienes via a 5-endo-trig Cyclization
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2. Uncommon 1,2-Migration of a Nitro Group Within a β-Nitrostyryl Moiety: Synthetic Scope and Mechanistic Details;European Journal of Organic Chemistry;2013-08-08
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5. Synthetic Exploitation of Halogenated Alkenes Containing Electron-Withdrawing Group (EWG): Access to Valuable 2,4-Dinitrothiophenes via Ring-Closing and Ring-Opening/Ring-Closing Protocols;HETEROCYCLES;2013
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