1971
DOI: 10.1039/j39710001627
|View full text |Cite
|
Sign up to set email alerts
|

The nuclear alkylation of pyrazines by ketones and aldehydes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
12
0

Year Published

1971
1971
2022
2022

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 15 publications
(12 citation statements)
references
References 0 publications
0
12
0
Order By: Relevance
“…A recent study by Bramwell et al (1971) demonstrated that if no catalyst is used in converting sodium into sodamide, pyrazine nuclear alkylation occurs preferentially at the six then three and finally five carbon position. Other metals besides sodium were investigated and it was found that potassium was even more effective than sodium in forming derivatives.…”
Section: Sodamide-ajkylpyrazine Reactionmentioning
confidence: 98%
“…A recent study by Bramwell et al (1971) demonstrated that if no catalyst is used in converting sodium into sodamide, pyrazine nuclear alkylation occurs preferentially at the six then three and finally five carbon position. Other metals besides sodium were investigated and it was found that potassium was even more effective than sodium in forming derivatives.…”
Section: Sodamide-ajkylpyrazine Reactionmentioning
confidence: 98%
“…Synthesis of 2-Alkyl-3-alkoxy-and 2-Alkyl-3-(alkylthio)pyrazines 20,21, and 23-33. The procedure used for the synthesis of these compounds was the same as that described previously (Bramwell et al, 1971(Bramwell et al, ,1972Masuda et al, 1981).…”
Section: Satoru Mihara* and Hideki Masudamentioning
confidence: 99%
“…Synthesis of Alkylpyrazines 1-7. Alkylpyrazines were prepared from the parent pyrazine by alkylation with the appropriate aldehyde in sodium dimethoxyethane solution (Bramwell et al, 1971).…”
mentioning
confidence: 99%