2016
DOI: 10.1080/00397911.2016.1234621
|View full text |Cite
|
Sign up to set email alerts
|

Efficient and facile synthesis of 5-arylindeno[2′,1′:5,6]pyrido[2,3-d] pyrimidine-2,4(3H)-dione and 7-arylbenzo[h]pyrimido[4,5-b]quinoline-8,10(5H,9H)-dione under mild conditions

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2020
2020
2022
2022

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 10 publications
0
1
0
Order By: Relevance
“…Rong et al carried out the one-step synthesis of indeno-fused pyridopyrimidine scaffolds 51 involving readily accessible 2-arylidene 1-indanone system under mild reaction conditions. 46 The authors employed 6-amino-1,3-dimethylpyrimidine 50 as the annulation partner to react with 2-arylidene 1-indanone 49 in the presence of catalytic amount of p -TsOH in refluxing acetonitrile resulting polyheterocyclic compounds 51 in excellent yields (Scheme 14). The reaction was also applicable for 2-arylidene dihydronaphthalenone systems.…”
Section: Synthesis Of Fused Scaffoldsmentioning
confidence: 99%
“…Rong et al carried out the one-step synthesis of indeno-fused pyridopyrimidine scaffolds 51 involving readily accessible 2-arylidene 1-indanone system under mild reaction conditions. 46 The authors employed 6-amino-1,3-dimethylpyrimidine 50 as the annulation partner to react with 2-arylidene 1-indanone 49 in the presence of catalytic amount of p -TsOH in refluxing acetonitrile resulting polyheterocyclic compounds 51 in excellent yields (Scheme 14). The reaction was also applicable for 2-arylidene dihydronaphthalenone systems.…”
Section: Synthesis Of Fused Scaffoldsmentioning
confidence: 99%