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Synlett 1993; 1993(11): 850-852
DOI: 10.1055/s-1993-22630
DOI: 10.1055/s-1993-22630
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.
Conversion of Esters to Amides with Amino Halo Stannylenes
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Publikationsverlauf
Publikationsdatum:
19. März 2002 (online)
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Amino chloro stannylenes have been prepared in situ using two different procedures: (1) reaction of an amine hydrochloride with Sn[N(TMS)2]2 and (2) reaction of a tin(II) amide with tin(II) chloride. These reagents are useful for the conversion of primary, α,β-unsaturated, or aromatic esters to amides.