The formation of Δ2-pyrrolines by base catalysed nitrile dimerisation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Nucleophilic substitution reactions of allylic halides carrying electron-withdrawing substituents in the γ-position. Formation of cyclopropanes from dimethyl 2-bromo-2-methylpropylidenemalonate
2. Synthesis of 1.1.2-trisubstituted spiro-[2.5]-octanes
3. Nucleophilic Ring-Opening Additions to 1,1-Disubstituted Cyclopropanes
4. Infrared and Ultraviolet Absorption Spectra of Enaminonitriles1a
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2. The photochemistry of an 1,1-dicyano-3-oxa-1-alkene and of its 3-aza analogue;Journal of Photochemistry and Photobiology A: Chemistry;2002-01
3. Condensation of (2-bromo-1-phenylethylidene)malononitrile with substituted thioureas: an unusual ring size effect;The Journal of Organic Chemistry;1990-07
4. The Reaction between Diazoalkanes and Allylic Halides Carrying Electronegative gamma-Substituents. 4. Conformational Equilibria of Highly Substituted 1-Pyrazolines.;Acta Chemica Scandinavica;1983
5. The Reaction between Diazoalkanes and Allylic Halides Carrying Electronegative gamma-Substituents. 2. Formation and Decomposition of Dimethyl 4-(1-Bromo-1-methylethyl)-5-aryl-4,5-dihydro-3H-3,3-pyrazoledicarboxylates.;Acta Chemica Scandinavica;1983
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