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 1990; 1990(10): 881-882
DOI: 10.1055/s-1990-27040
DOI: 10.1055/s-1990-27040
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.
Sterically Hindered Bases. Synthesis of 2,4,6-Trisubstituted Pyrimidines
Further Information
Publication History
Publication Date:
17 September 2002 (online)
A new method for the synthesis of sterically hindered pyrimidines 7 by the reaction of alkynes 5 with nitriles 6 in the presence of trifluoromethanesulfonic acid is described. The pKa*-values of some of the synthesized pyrimidines 7, which can be used as nonnucleophilic bases, were determined in 50% aqueous ethanol.