Reaktionen mit Aziridinen, 42 1) Die Regioselektivität der Ringöffnung von aktivierten 2,2‐Dimethylaziridinen durch Carbanionen des β‐Dicarbonyltyps. Einfluß der Größe des Nucleophils
Author:
Affiliation:
1. Pharmazeutisch‐Chemisches Institut der Universität Heidelberg, Im Neuenheimer Feld 364, D‐6900 Heidelberg
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19871200720
Reference20 articles.
1. Reaktionen mit Aziridinen, 41 Hoch regioselektive (anomale) Ringöffnung von 1‐Benzoyl‐2,2‐dimethylaziridin durch einfache Nitril‐Anionen
2. Nucleophilic cleavage of 2,2-dimethylaziridines: competition between SN2 and postulated “SET” mechanism.
3. Reactions with aziridines. 33. Arene hydrides. Part 1. Highly regioselective ring cleavage of N-acylaziridines by "anthracene hydride" (anion of 9,10-dihydroanthracene). Intermediacy of a carbonyl adduct. Influence of nitrogen inversion on the ring opening
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1. Enantioselective Synthesis of 4,5-Dihydropyrroles via Domino Ring-Opening Cyclization (DROC) ofN-Activated Aziridines with Malononitrile;The Journal of Organic Chemistry;2013-02-19
2. The regioselectivity of the ring opening of 1-activated or nonactivated 2-alkoxycarbonyl or 2-cyanoaziridines by carbanions of the dicarbonyl compounds;Journal of Heterocyclic Chemistry;2009-03-11
3. Ring opening of aziridines by aromatic thiols followed by amino-substitution;Tetrahedron Letters;2006-06
4. Nucleophilic ring opening of aziridines;J PRAK CHEM-CHEM ZTG;1999
5. Synthesis of α-amino acids by ring opening of aziridine-2-carboxylates with carbon nucleophiles;Tetrahedron Letters;1995-01
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