This submission belongs to the session a. General Organic Synthesis of the event The 1st International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Sep, 1997
Citation
Natalie V. Sivova, Ekaterina A. Kishko, Anatoly D. Shutalev, A New Approach to 5-Functionalized Pyrimidine-2-Thiones, in Proceedings of The 1st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1997, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-1-02012
Share
Email
Facebook
Twitter
LinkedIn
A New Approach to 5-Functionalized Pyrimidine-2-Thiones
Anatoly D. Shutalev 1
Ekaterina A. Kishko 1
Natalie V. Sivova 1
1. Department of Organic Chemistry, State Academy of Fine Chemical Technology, Vernadsky Avenue 86, Moscow 117571, Russia.
Abstract
A new general convenient approach to the synthesis of pyrimidine-2-thiones/ones has been developed. This approach is based on the preparation of a-tosyl and a-azido substituted thioureas and ureas followed by the reaction with sodium enolates of carbonyl compounds.
Keywords
Thioureas
ureas
aldehydes
p-toluenesulfinic acid
hydrazoic acid
amidoalkylation
C-H acids
hexahydropyrimidine-2-thiones/ones
1,2,3,4-tetrahydropyrimidine-2-thiones/ones.
A Straightforward Route to Enantiopure Pyrrolizidines by Cycloaddition to Pyrroline N-Oxides Derived from the Chiral Pool
New Synthetic Application of Ureidoalkylation in Heterocyclic Chemistry