2015
DOI: 10.1002/chin.201537194
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Indolizines and Pyrrolo[1,2‐c]pyrimidines Decorated with a Pyrimidine and a Pyridine Unit Respectively.

Abstract: Indolizines and Pyrrolo[1,2-c]pyrimidines Decorated with a Pyrimidine and a Pyridine UnitRespectively. -4-(4-Pyridyl)pyrimidine (I) and its 3-pyridyl-isomer (V) undergo quaternization reactions at the pyridine ring in reactions with bromoacetophenones, whilst the 4-(2-pyridyl)pyrimidine (VIII) suffers quaternization at the pyrimidine ring due to steric hindrance. 1,3-Dipolar cycloaddition of the N-ylides thus obtained with alkynes (II) provides access to new indolizines or pyrrolopyrimidines, respectively. -(P… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?