2015
DOI: 10.1007/s11172-015-0835-4
|View full text |Cite
|
Sign up to set email alerts
|

Iron(iii) phosphate-catalyzed synthesis of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-ones

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
5
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 8 publications
(5 citation statements)
references
References 14 publications
0
5
0
Order By: Relevance
“…Dibenzo[ c ]acridine 114 synthesis catalysed by iron (III)phosphate was reported in 2015. [ 72 ] This one‐pot reaction involved dimedone 48 , aromatic aldehydes 30 and 1‐naphthylamine 113 as the substrates (Scheme 41). The protocol could achieve good yields within short duration.…”
Section: Classificationmentioning
confidence: 99%
“…Dibenzo[ c ]acridine 114 synthesis catalysed by iron (III)phosphate was reported in 2015. [ 72 ] This one‐pot reaction involved dimedone 48 , aromatic aldehydes 30 and 1‐naphthylamine 113 as the substrates (Scheme 41). The protocol could achieve good yields within short duration.…”
Section: Classificationmentioning
confidence: 99%
“…Maltose-dimethylurea (DMU)-NH 4 Cl/ 90°C [22] NaHSO 4, water/rt-60°C [77] FePO 4 / rt/EtOH [24] SSA/ Solvent-free/ 80°C [67] 200, 90, 60 [71] Er-MOF/ Solvent-free/ rt [80] EtOH/ rt/ us [70] TEACB/ reflux EtOH [83] 24(h), 12, 60, 70 63, 98, 90, 95 The promising points for the presented catalytic system are simplicity of product isolation, recyclability, high efficiency, short reaction time and high yield. The high catalytic ability of the presented catalyst is due to the presence of two acidic functional groups with strong none bonded repulsion.…”
Section: Discussionmentioning
confidence: 99%
“…[22,23] The existence of these properties provides reasons for proposing a variety of methods for the synthesis of these compounds. [22,[24][25][26][27][28][29][30] Liter-ature surveys shows that the reported synthetic methodologies for elaboration of these simple heterocyclic compounds are time consuming, tedious work-up and low yielding of target molecules. The chemistry of quinazolines and quinazolinones have been comprehinslvly reviewed by Guiry and coworkers.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…A novel, modified synthetic strategy for benzo[ c ]acridine derivatives has been developed using aromatic aldehydes in benzene which affords moderate to excellent yields of the products (Scheme ) …”
Section: Synthesis Of Heterocycles Based On the Ring Sizementioning
confidence: 99%