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Synlett 1991; 1991(9): 631-632
DOI: 10.1055/s-1991-20821
DOI: 10.1055/s-1991-20821
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.
(Bromomethyl) lithium: Efficient in situ Reactions
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Publikationsverlauf
Publikationsdatum:
07. März 2002 (online)
(Bromomethyl)lithium has been generated by the addition of butyllithium to dibromomethane in the presence of suitable substrates in tetrahydrofuran at -78 °C. Aldehydes or ketones yielded oxiranes (85-93%), triisopropyl borate yielded diisopropyl (bromomethyl)boronate (89%), and boronic esters without functional substituents underwent methylene insertion into the carbon-boron bond (95-97%).