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-00000084.xml
Synthesis 1985; 1985(11): 1062-1067
DOI: 10.1055/s-1985-31430
DOI: 10.1055/s-1985-31430
communication
© 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.Allen-1,1-dicarboxamide durch Umallenierung von 1,3-Bis[dialkylamino]-1,3-diethoxyallenen mit disubstituierten Malonyl-chloriden
Further Information
Publication History
Publication Date:
27 September 2002 (online)
PDF Download(opens in new window) Permissions and Reprints(opens in new window) All articles of this category(opens in new window)
Allene-1,1-dicarboxamides by Transallenation of 1,3-Bis[dialkylamino]-1,3-diethoxyallenes with Disubstituted Malonyl Chlorides N,N,N′,N′-Tetrasubstituted malonic diamides are converted into 1,3-bis[dialkyl(aryl)-amino]-1,3-diethoxyallenes via a four-step O-ethylation - deprotonation - O-ethylation - deprotanation sequence using triethyloxonium tetrafluoroborate as ethylating agent. The 1,3-bis[dialkylamino]-1,3-diethoxyallenes thus prepared react with disubstituted malonyl chlorides to give N,N,N′,N′-tetraalkylallene-1,1-dicarboxamides.