RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 1988; 1988(1): 70-72
DOI: 10.1055/s-1988-27469
DOI: 10.1055/s-1988-27469
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.Facile Preparation of 6-Substituted Uracils
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
12. September 2002 (online)

6-Substituted 2,4-bis(methylthio)pyrimidines 5 are obtained in the reaction of (i) 5-bromo-2,4-bis(methylthio)pyrimidine (1) with aryllithium and heteroaryllithium reagents, followed by spontaneous dehydrobromination of the intermediate bromo dihydropyrimidines 3 or (ii) 2,4-bis(methylthio)pyrimidine (2) with alkyllithium, aryllithium, and heteroaryllithium reagents, followed by aromatization of the intermediate dihydropyrimidines 4 with DDQ. Hydrolysis of these compounds produces 6-substituted uracils 6.