Abstract
2 : 3 : 5 : 6-Substituted 4-pyrimidones are readily synthesised by condensation of imidoyl chlorides with methyl or ethyl α-alkyl-β- aminocrotonates.
| Language | English |
|---|---|
| Pages | 4665-4700 |
| Number of pages | 36 |
| Journal | Journal of the Chemical Society (Resumed) |
| Publication status | Published - 1956 |
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A New Synthesis of 2 : 3: 5: 6-Substituted 4-Pyrimidones. / Staskun, Benjamin; Stephen, Henry.
In: Journal of the Chemical Society (Resumed), 1956, p. 4665-4700.Research output: Contribution to journal › Article › Research › peer-review
TY - JOUR
T1 - A New Synthesis of 2
T2 - Journal of the Chemical Society (Resumed)
AU - Staskun, Benjamin
AU - Stephen, Henry
PY - 1956
Y1 - 1956
N2 - 2 : 3 : 5 : 6-Substituted 4-pyrimidones are readily synthesised by condensation of imidoyl chlorides with methyl or ethyl α-alkyl-β- aminocrotonates.
AB - 2 : 3 : 5 : 6-Substituted 4-pyrimidones are readily synthesised by condensation of imidoyl chlorides with methyl or ethyl α-alkyl-β- aminocrotonates.
UR - http://www.scopus.com/inward/record.url?scp=37049043024&partnerID=8YFLogxK
M3 - Article
SP - 4665
EP - 4700
JO - Journal of the Chemical Society (Resumed)
JF - Journal of the Chemical Society (Resumed)
SN - 0368-1769
ER -