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Synlett 1994; 1994(8): 651-652
DOI: 10.1055/s-1994-22962
DOI: 10.1055/s-1994-22962
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.
A New and Selective α′-Bromination of α,β-Unsaturated Ketones
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Publikationsverlauf
Publikationsdatum:
18. September 2002 (online)
α′-Bromination of α,β-unsaturated ketones was carried out via trialkylsilyl dienol ethers with phenyltrimethylammonium tribromide. This reagent, which has not been previously used to brominate such derivatives, allows a high degree of selectivity under mild reaction conditions with the further advantage of not requiring the isolation of the silyl intermediates. The bromination selectivity is dependent on the trialkylsilyl group present on the dienol ether.