Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2000; 2000(10): 1464-1466
DOI: 10.1055/s-2000-7626
DOI: 10.1055/s-2000-7626
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.
1,2-Diaza-1,3-butadienes as Powerful Tools in the Synthesis of New 1,6-Dithia-4,9-diazaspiro[4.4]non-2-enes and 1-Oxa-6-thia-4,9-diazaspiro[4.4]non-7-enes
Further Information
Publication History
Publication Date:
31 December 2000 (online)
1,2-Diaza-1,3-butadienes react with 2-mercapto-2-thiazoline to give 1,4-adducts that in turn produce new 1,6-dithia-4,9-diazaspiro[4.4]non-2-ene derivatives. The same reactants treated with oxazolidine-2-thione directly afford new 1-oxa-6-thia-4,9-diazaspiro[4.4]non-7-ene derivatives.
1,2-diaza-1,3-butadienes - thiols - nucleophilic additions - annulation - spiro compounds