2009
DOI: 10.1016/j.tetlet.2009.10.055
|View full text |Cite
|
Sign up to set email alerts
|

Atom-efficient and environment-friendly multicomponent synthesis of amidoalkyl naphthols catalyzed by P2O5

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

2
28
0

Year Published

2010
2010
2014
2014

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 132 publications
(30 citation statements)
references
References 47 publications
2
28
0
Order By: Relevance
“…Therefore, the following mechanism can be suggested for the synthesis of amidoalkyl naphthols (Scheme 2) [16][17][18][19].…”
Section: Preparation Of 1-amidoalkyl-2-naphthols Under Solvent-free Cmentioning
confidence: 99%
See 1 more Smart Citation
“…Therefore, the following mechanism can be suggested for the synthesis of amidoalkyl naphthols (Scheme 2) [16][17][18][19].…”
Section: Preparation Of 1-amidoalkyl-2-naphthols Under Solvent-free Cmentioning
confidence: 99%
“…In recent years, ZrOCl 2 [9] [14], VB 1 [15], P 2 O 5 [16], Yb(OTf) 3 Bmim BF 4 [17], CuPMo [18], NKC-9 [19], and H 3 Mo 12 O 40 P [20] have been utilized, as catalysts, for this synthesis. In continuation of our interest in the application of N,N,N',N'-tetrabromobenzene-1,3-disulfonamide [TBBDA] [21] (Fig.…”
Section: Introductionmentioning
confidence: 99%
“…Solventfree multicomponent reactions offer a wide range of possibilities for the efficient construction of highly complex molecules in a single step, thus avoiding complicated purification operations and allowing savings of both solvents and reagents. 5,6 Functionalized nitrogen-heterocycles play a prominent role in medicinal chemistry and they have been intensively used as scaffolds for drug development. In this context fused pyrimidine derivatives are of particular interest because of their pharmacological profile.…”
Section: Introductionmentioning
confidence: 99%
“…al 2008), Brösted acidic ionic liquid (Hajipour, A. R. et. al 2009), P 2 O 5 (Nandi, G. C. et. al 2009), cyanuric chloride (Mahdavinia, G. H. et.…”
Section: Introductionmentioning
confidence: 99%