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QSAR analysis on Spodoptera litura antifeedant activities for flavone derivatives

The Science of the total environment, 2009-12, Vol.408 (2), p.277-285

2009

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An Efficient Protocol for the Synthesis of Quinoxaline Derivatives at Room Temperature Using Recyclable Alumina-Supported Heteropolyoxometalates

TheScientificWorld, 2012-01, Vol.2012, p.174784-8

2012

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Preyssler heteropolyacid H14[NaP5W29MoO110]: A heterogeneous, green and recyclable catalyst used for the protection of functional groups in organic synthesis

Chemical engineering journal (1996), 2010-07, Vol.161 (3), p.355-362

2010

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Quantitative Structure–Activity Relationships of Mosquito Larvicidal Chalcone Derivatives

Journal of agricultural and food chemistry, 2012-01, Vol.60 (2), p.692-697

2012

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A theoretical–experimental study of Wells-Dawson phospho-tungstic heteropolyacid: An explanation of the pseudoliquid or surface-type behaviour

Applied catalysis. A, General, 2010-04, Vol.378 (1), p.114-118

2010

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Wells–Dawson heteropolyacid as reusable catalyst for sustainable synthesis of flavones

Applied catalysis. A, General, 2011-09, Vol.404 (1), p.68-73

2011

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Preyssler catalyst: An efficient catalyst for esterification of cinnamic acids with phenols and imidoalcohols

Applied catalysis. A, General, 2010-02, Vol.374 (1), p.110-119

2010

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Sustainable Synthesis of Flavonoid Derivatives, QSAR Study and Insecticidal Activity against the Fall Armyworm, Spodoptera frugiperda (Lep.: Noctuidae)

Journal of agricultural and food chemistry, 2010-05, Vol.58 (10), p.6290-6295

2010

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Solvent-free catalytic preparation of 1,1-diacetates from aldehydes using a Wells–Dawson acid (H 6P 2W 18O 62·24H 2O)

Tetrahedron letters, 2003-02, Vol.44 (6), p.1301-1303

2003

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QSAR prediction of inhibition of aldose reductase for flavonoids

Bioorganic & medicinal chemistry, 2008-08, Vol.16 (15), p.7470-7476

2008

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Simple halogen-free synthesis of aryl cinnamates using Mo-Keggin heteropoly acids as catalyst

Pure and applied chemistry, 2012-01, Vol.84 (3), p.529-540

2012

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QSAR modeling of the interaction of flavonoids with GABA(A) receptor

European journal of medicinal chemistry, 2008-08, Vol.43 (8), p.1593-1602

2008

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suitable preparation of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines and their ring homologs with a reusable Preyssler heteropolyacid as catalyst

Molecular diversity, 2010-11, Vol.14 (4), p.803-807

2010

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Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones

Journal of porous materials, 2013-12, Vol.20 (6), p.1433-1440

2013

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Synthesis of substituted flavones and chromones using a Wells-Dawson heteropolyacid as catalyst

ARKIVOC, 2008-03, Vol.2008 (11), p.123-130

2008

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Direct esterification of cinnamic acids with phenols and imidoalcohols: A simple heteropolyacid-catalyzed procedure

ARKIVOC, 2008-05, Vol.2008 (12), p.269-276

2008

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Preyssler catalyst-promoted rapid, clean, and efficient condensation reactions for 3H-1,5-benzodiazepine synthesis in solvent-free conditions

Tetrahedron letters, 2013-11, Vol.54 (48), p.6574-6579

2013

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Spectroscopic and theoretical study of 2-acetylphenyl-2-naphthoate

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2009, Vol.71 (5), p.1989-1998

2009

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A Simple and Mild Acylation of Alcohols, Phenols, Amines, and Thiols with a Reusable Heteropoly Acid Catalyst (H 6 P 2 W 18 O 62 ·24 H 2 O)

Journal of chemistry, 2008, Vol.5 (3), p.641-647

2008

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Hydrogen Bonding in Nitroanilines: Neutron Diffraction Study of m-Nitroaniline at 100 K

Chemistry of materials, 2000-11, Vol.12 (11), p.3342-3346

2000

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Preyssler heteropolyacid H 14[NaP 5W 29MoO 110]: A heterogeneous, green and recyclable catalyst used for the protection of functional groups in organic synthesis

Chemical engineering journal (Lausanne, Switzerland : 1996), 2010-07, Vol.161 (3), p.355-362

2010

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Single-step synthesis of 4-phenyl and 3,4-dihydro-4-phenyl coumarins using a recyclable Preyssler heteropolyacid catalyst under solvent-free reaction conditions

Research on chemical intermediates, 2015-12, Vol.41 (12), p.10109-10123

2015

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Silicagel-supported H6P2W18O62.24H2O: a reusable catalyst to prepare diphenylmethyl (DPM) ethers

ARKIVOC, 2007-01, Vol.2007 (1), p.1-8

2007

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Quantitative Structure-Activity Relationships of Mosquito Larvicida Chalcone Derivatives

Journal of agricultural and food chemistry, 2012, Vol.60 (2), p.692-697

2012

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Solvent-Free Approach to 3,4-Dihydropyrimidin-2(1H)-(thio)ones: Biginelli Reaction Catalyzed by a Wells-Dawson Reusable Heteropolyacid

Synthetic communications, 2007-11, Vol.37 (22), p.3907-3916

2007

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QSAR analysis on Spodoptera litura antifeedant activities for flavone derivatives

An Efficient Protocol for the Synthesis of Quinoxaline Derivatives at Room Temperature Using Recyclable Alumina-Supported Heteropolyoxometalates

Preyssler heteropolyacid H14[NaP5W29MoO110]: A heterogeneous, green and recyclable catalyst used for the protection of functional groups in organic synthesis

Quantitative Structure–Activity Relationships of Mosquito Larvicidal Chalcone Derivatives

A theoretical–experimental study of Wells-Dawson phospho-tungstic heteropolyacid: An explanation of the pseudoliquid or surface-type behaviour

Wells–Dawson heteropolyacid as reusable catalyst for sustainable synthesis of flavones

Preyssler catalyst: An efficient catalyst for esterification of cinnamic acids with phenols and imidoalcohols

Sustainable Synthesis of Flavonoid Derivatives, QSAR Study and Insecticidal Activity against the Fall Armyworm, Spodoptera frugiperda (Lep.: Noctuidae)

Solvent-free catalytic preparation of 1,1-diacetates from aldehydes using a Wells–Dawson acid (H 6P 2W 18O 62·24H 2O)

QSAR prediction of inhibition of aldose reductase for flavonoids

Simple halogen-free synthesis of aryl cinnamates using Mo-Keggin heteropoly acids as catalyst

QSAR modeling of the interaction of flavonoids with GABA(A) receptor

suitable preparation of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines and their ring homologs with a reusable Preyssler heteropolyacid as catalyst

Mesoporous titania/tungstophosphoric acid composites: suitable synthesis of flavones

Synthesis of substituted flavones and chromones using a Wells-Dawson heteropolyacid as catalyst

Direct esterification of cinnamic acids with phenols and imidoalcohols: A simple heteropolyacid-catalyzed procedure

Preyssler catalyst-promoted rapid, clean, and efficient condensation reactions for 3H-1,5-benzodiazepine synthesis in solvent-free conditions

Spectroscopic and theoretical study of 2-acetylphenyl-2-naphthoate

A Simple and Mild Acylation of Alcohols, Phenols, Amines, and Thiols with a Reusable Heteropoly Acid Catalyst (H 6 P 2 W 18 O 62 ·24 H 2 O)

Hydrogen Bonding in Nitroanilines: Neutron Diffraction Study of m-Nitroaniline at 100 K

Preyssler heteropolyacid H 14[NaP 5W 29MoO 110]: A heterogeneous, green and recyclable catalyst used for the protection of functional groups in organic synthesis

Single-step synthesis of 4-phenyl and 3,4-dihydro-4-phenyl coumarins using a recyclable Preyssler heteropolyacid catalyst under solvent-free reaction conditions

Silicagel-supported H6P2W18O62.24H2O: a reusable catalyst to prepare diphenylmethyl (DPM) ethers

Quantitative Structure-Activity Relationships of Mosquito Larvicida Chalcone Derivatives

Solvent-Free Approach to 3,4-Dihydropyrimidin-2(1H)-(thio)ones: Biginelli Reaction Catalyzed by a Wells-Dawson Reusable Heteropolyacid

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