A New Synthesis of 2: 3: 5: 6-Substituted 4-Pyrimidones

Benjamin Staskun; Henry Stephen

A New Synthesis of 2: 3: 5: 6-Substituted 4-Pyrimidones

Benjamin Staskun^*, Henry Stephen

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

Abstract

2 : 3 : 5 : 6-Substituted 4-pyrimidones are readily synthesised by condensation of imidoyl chlorides with methyl or ethyl α-alkyl-β- aminocrotonates.

Original language	English
Pages (from-to)	4665-4700
Number of pages	36
Journal	Journal of the Chemical Society (Resumed)
Publication status	Published - 1956

Cite this

@article{50f2b1b0c4404d0ab4cabbf5aa52c9e0,

title = "A New Synthesis of 2: 3: 5: 6-Substituted 4-Pyrimidones",

abstract = "2 : 3 : 5 : 6-Substituted 4-pyrimidones are readily synthesised by condensation of imidoyl chlorides with methyl or ethyl α-alkyl-β- aminocrotonates.",

author = "Benjamin Staskun and Henry Stephen",

year = "1956",

language = "English",

pages = "4665--4700",

journal = "Journal of the Chemical Society (Resumed)",

issn = "0368-1769",

publisher = "Chemical Society",

}

TY - JOUR

T1 - A New Synthesis of 2

T2 - 3: 5: 6-Substituted 4-Pyrimidones

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

AN - SCOPUS:37049043024

SN - 0368-1769

SP - 4665

EP - 4700

JO - Journal of the Chemical Society (Resumed)

JF - Journal of the Chemical Society (Resumed)

ER -

A New Synthesis of 2: 3: 5: 6-Substituted 4-Pyrimidones

Abstract

Other files and links

Fingerprint

Cite this