Regioselective cycloaddition of 1,2‐disubstituted aziridines to heterocumulenes catalyzed by organoantimony halides
Author:
Affiliation:
1. Department of Applied Chemistry, Faculty of Engineering, Osaka University, Yamada‐Oka, Suita, Osaka 565 (Japan)
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19891221232
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3. Reductive ring opening of N-benzoylaziridine by anthracene hydride (anion of 9,10-dihydroanthracene) via base-induced fragmentation of the intermediate carbonyl adduct
4. Reaktionen mit Aziridinen, 42 1) Die Regioselektivität der Ringöffnung von aktivierten 2,2‐Dimethylaziridinen durch Carbanionen des β‐Dicarbonyltyps. Einfluß der Größe des Nucleophils
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