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Supported Palladium Nanoparticles that Catalyze Aminocarbonylation of Aryl Halides with Amines using Oxalic Acid as a Sustainable CO Source

Chemistry : a European journal, 2019-03, Vol.25 (16), p.4067-4071

2019

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Benzosuberene-sulfone analogues synthesis from Cedrus deodara oil and their therapeutic evaluation by computational analysis to treat type 2 diabetes

Bioorganic chemistry, 2021-07, Vol.112, p.104860-104860, Article 104860

2021

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Solid Supported Palladium(0) Nanoparticles: An Efficient Heterogeneous Catalyst for Regioselective Hydrosilylation of Alkynes and Suzuki Coupling of β-Arylvinyl Iodides

Catalysis letters, 2014-09, Vol.144 (9), p.1530-1536

2014

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Supported palladium nanoparticle‐catalysed Suzuki–Miyaura cross‐coupling approach for synthesis of aminoarylbenzosuberene analogues from natural precursor

Applied organometallic chemistry, 2017-11, Vol.31 (11), p.n/a

2017

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Supported Palladium Nanoparticle-Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C1 Source

Organic letters, 2015-11, Vol.17 (21), p.5352-5355

2015

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Phosphine-Built-in Porous Organic Cage for Stabilization and Boosting the Catalytic Performance of Palladium Nanoparticles in Cross-Coupling of Aryl Halides

ACS applied materials & interfaces, 2020-11, Vol.12 (47), p.53141-53149

2020

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Ligand‐Free FeCl2‐Catalyzed α‐Alkylation of Ketones with Alcohols

Asian journal of organic chemistry, 2019-10, Vol.8 (10), p.1858-1861

2019

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Manganese Catalyzed α‑Alkylation of Nitriles with Primary Alcohols

ACS catalysis, 2018-10, Vol.8 (10), p.9226-9231

2018

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Microwave assisted solvent and catalyst free method for novel classes of β-enaminoester and acridinedione synthesis

RSC advances, 2013-01, Vol.3 (26), p.10335-10340

2013

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Supported Palladium Nanoparticle-Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C 1 Source

Organic letters, 2015-11, Vol.17 (21), p.5352-5355

2015

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Supported Palladium Nanoparticle Catalyzed α‑Alkylation of Ketones Using Alcohols as Alkylating Agents

ACS sustainable chemistry & engineering, 2017-11, Vol.5 (11), p.9683-9691

2017

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Oxalic Acid as Sustainable CO Source for Pyrrolone‐Fused Benzosuberenes Synthesis through Palladium Catalyzed Carbonylative Cyclization

ChemistrySelect (Weinheim), 2017-06, Vol.2 (17), p.4626-4629

2017

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Iodine(III)‐Promoted Ring Contractive Cyanation of Exocyclic β‐Enaminones for the Synthesis of Cyanocyclopentanones

Advanced synthesis & catalysis, 2017-07, Vol.359 (13), p.2209-2214

2017

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Supported palladium nanoparticles-catalyzed decarboxylative coupling approaches to aryl alkynes, indoles and pyrrolines synthesis

RSC advances, 2016-01, Vol.6 (75), p.71117-71121

2016

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Oxidative “reverse-esterification” of ethanol with benzyl/alkyl alcohols or aldehydes catalyzed by supported rhodium nanoparticles

Green chemistry : an international journal and green chemistry resource : GC, 2016-01, Vol.18 (5), p.1206-1211

2016

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Ligand‐Free FeCl 2 ‐Catalyzed α‐Alkylation of Ketones with Alcohols

Asian journal of organic chemistry, 2019-10, Vol.8 (10), p.1858-1861

2019

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Iodine(III)-Promoted Ring Contractive Cyanation of Exocyclic [beta]-Enaminones for the Synthesis of Cyanocyclopentanones

Advanced synthesis & catalysis, 2017-07, Vol.359 (13), p.2209

2017

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Oxidative "reverse-esterification" of ethanol with benzyl/alkyl alcohols or aldehydes catalyzed by supported rhodium nanoparticlesElectronic supplementary information (ESI) available. See DOI: 10.1039/c5gc02513c

2016-02

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ChemInform Abstract: Supported Palladium Nanoparticles‐Catalyzed Decarboxylative Coupling Approaches to Aryl Alkynes, Indoles and Pyrrolines Synthesis

ChemInform, 2016-11, Vol.47 (50), p.no-no

2016

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Supported palladium nanoparticles-catalyzed decarboxylative coupling approaches to aryl alkynes, indoles and pyrrolines synthesisElectronic supplementary information (ESI) available: Experimental details and spectral data. See DOI: 10.1039/c6ra12046f

2016-07

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ChemInform Abstract: Supported Palladium Nanoparticle‐Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C1 Source

ChemInform, 2016-03, Vol.47 (12), p.no-no

2016

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ChemInform Abstract: Supported Palladium Nanoparticle‐Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C 1 Source

ChemInform, 2016-03, Vol.47 (12)

2016

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Multidrug salt forms of norfloxacin with non-steroidal anti-inflammatory drugs: solubility and membrane permeability studies

CrystEngComm, 2018, Vol.20 (41), p.6420-6429

2018

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Remarkably Distinct Mechanical Flexibility in Three Structurally Similar Semiconducting Organic Crystals Studied by Nanoindentation and Molecular Dynamics

Chemistry of materials, 2019-02, Vol.31 (4), p.1391-1402

2019

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ABT-450/r–Ombitasvir and Dasabuvir with or without Ribavirin for HCV

The New England journal of medicine, 2014-05, Vol.370 (21), p.1983-1992

2014

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Supported Palladium Nanoparticles that Catalyze Aminocarbonylation of Aryl Halides with Amines using Oxalic Acid as a Sustainable CO Source

Benzosuberene-sulfone analogues synthesis from Cedrus deodara oil and their therapeutic evaluation by computational analysis to treat type 2 diabetes

Solid Supported Palladium(0) Nanoparticles: An Efficient Heterogeneous Catalyst for Regioselective Hydrosilylation of Alkynes and Suzuki Coupling of β-Arylvinyl Iodides

Supported palladium nanoparticle‐catalysed Suzuki–Miyaura cross‐coupling approach for synthesis of aminoarylbenzosuberene analogues from natural precursor

Supported Palladium Nanoparticle-Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C1 Source

Phosphine-Built-in Porous Organic Cage for Stabilization and Boosting the Catalytic Performance of Palladium Nanoparticles in Cross-Coupling of Aryl Halides

Ligand‐Free FeCl2‐Catalyzed α‐Alkylation of Ketones with Alcohols

Manganese Catalyzed α‑Alkylation of Nitriles with Primary Alcohols

Microwave assisted solvent and catalyst free method for novel classes of β-enaminoester and acridinedione synthesis

Supported Palladium Nanoparticle-Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C 1 Source

Supported Palladium Nanoparticle Catalyzed α‑Alkylation of Ketones Using Alcohols as Alkylating Agents

Oxalic Acid as Sustainable CO Source for Pyrrolone‐Fused Benzosuberenes Synthesis through Palladium Catalyzed Carbonylative Cyclization

Iodine(III)‐Promoted Ring Contractive Cyanation of Exocyclic β‐Enaminones for the Synthesis of Cyanocyclopentanones

Supported palladium nanoparticles-catalyzed decarboxylative coupling approaches to aryl alkynes, indoles and pyrrolines synthesis

Oxidative “reverse-esterification” of ethanol with benzyl/alkyl alcohols or aldehydes catalyzed by supported rhodium nanoparticles

Ligand‐Free FeCl 2 ‐Catalyzed α‐Alkylation of Ketones with Alcohols

Iodine(III)-Promoted Ring Contractive Cyanation of Exocyclic [beta]-Enaminones for the Synthesis of Cyanocyclopentanones

Oxidative "reverse-esterification" of ethanol with benzyl/alkyl alcohols or aldehydes catalyzed by supported rhodium nanoparticlesElectronic supplementary information (ESI) available. See DOI: 10.1039/c5gc02513c

ChemInform Abstract: Supported Palladium Nanoparticles‐Catalyzed Decarboxylative Coupling Approaches to Aryl Alkynes, Indoles and Pyrrolines Synthesis

Supported palladium nanoparticles-catalyzed decarboxylative coupling approaches to aryl alkynes, indoles and pyrrolines synthesisElectronic supplementary information (ESI) available: Experimental details and spectral data. See DOI: 10.1039/c6ra12046f

ChemInform Abstract: Supported Palladium Nanoparticle‐Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C1 Source

ChemInform Abstract: Supported Palladium Nanoparticle‐Catalyzed Carboxylation of Aryl Halides, Alkenylsilanes, and Organoboronic Acids Employing Oxalic Acid as the C 1 Source

Multidrug salt forms of norfloxacin with non-steroidal anti-inflammatory drugs: solubility and membrane permeability studies

Remarkably Distinct Mechanical Flexibility in Three Structurally Similar Semiconducting Organic Crystals Studied by Nanoindentation and Molecular Dynamics

ABT-450/r–Ombitasvir and Dasabuvir with or without Ribavirin for HCV

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