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Synlett 1996; 1996(9): 847-849
DOI: 10.1055/s-1996-5605
DOI: 10.1055/s-1996-5605
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Preparation and Ring-Opening Reactions of N-Diphenylphosphinyl Vinyl Aziridines
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)
N-Diphenylphosphinyl-3-ethenyl-2-phenylaziridine (1) and N-diphenylphosphinyl-3-ethenyl-2-(4-bromophenyl)aziridine (2) are prepared by reaction of α-bromo allyllithium with N-diphenylphosphinyl aldimines in the presence of zinc chloride. (1) and (2) undergo efficient SN2’ ring-opening reaction with several nucleophiles.
Aziridines - diphenylphosphinyl - SN2’