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Synthesis 1999; 1999(5): 787-792
DOI: 10.1055/s-1999-3468
DOI: 10.1055/s-1999-3468
paper
© 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.
Synthese nichtanellierter 2,6-Imino-2H,6H-1,5-dithiocine
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Publikationsverlauf
Publikationsdatum:
31. Dezember 1999 (online)
![](https://www.thieme-connect.de/media/synthesis/199905/lookinside/thumbnails/10.1055-s-1999-3468-1.jpg)
Substituted secondary β-enaminothioketones of general type R1CSCR2=CHNHR3 react in acetic acid yielding the title compounds. The structure of these molecules was confirmed by 1H and 13C NMR spectroscopy and in one case by means of X-ray crystallographic investigations.
enaminothioketones - β-thioxoaldehydes - 2,6-imino-2H,6H-1,5-dithiocines - [4+2]-cycloaddition