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Advances in Microwave Chemistry

1, 2018

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Metal‐Free Cross‐Dehydrogenative Coupling (CDC): Molecular Iodine as a Versatile Catalyst/Reagent for CDC Reactions

Chemistry, an Asian journal, 2019-01, Vol.14 (1), p.6-30

2019

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Bismuth Nitrate-Catalyzed Versatile Michael Reactions

Journal of organic chemistry, 2003-03, Vol.68 (6), p.2109-2114

2003

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Synthesis of Medicinally Privileged Heterocycles through Dielectric Heating

Current medicinal chemistry, 2017-01, Vol.24 (41), p.4596

2017

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Drug Repurposing Strategy (DRS): Emerging Approach to Identify Potential Therapeutics for Treatment of Novel Coronavirus Infection

Frontiers in molecular biosciences, 2021-02, Vol.8, p.628144

2021

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Beta-Lactams: Novel Synthetic Pathways and Applications

1, 2017

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A microwave-assisted bismuth nitrate-catalyzed unique route toward 1,4-dihydropyridines

Molecules (Basel, Switzerland), 2012-03, Vol.17 (3), p.2643-2662

2012

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Advances in Hydrogen Production from Natural Gas Reforming

Advanced energy and sustainability research, 2021-11, Vol.2 (11), p.n/a

2021

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Microwave-induced Bismuth Salts-mediated Synthesis of Molecules of Medicinal Interests

Current medicinal chemistry, 2017-01, Vol.24 (41), p.4677

2017

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An expeditious iodine-catalyzed synthesis of 3-pyrrole-substituted 2-azetidinones

Molecules (Basel, Switzerland), 2012-10, Vol.17 (10), p.11570-11584

2012

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Polysaccharides from Dolichos biflorus Linn and Trachyspermum ammi Linn seeds: isolation, characterization and remarkable antimicrobial activity

BMC chemistry, 2017-11, Vol.11 (1), p.1-10

2017

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An expeditious synthesis of N-substituted pyrroles via microwave-induced iodine-catalyzed reactions under solventless conditions

Molecules (Basel, Switzerland), 2010-04, Vol.15 (4), p.2520-2525

2010

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Green Approaches in Medicinal Chemistry for Sustainable Drug Design

Banik, Bimal

1, 2020

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A selective, expeditious and sustainable entry en route to benzopyrazines and bis-benzopyrazines

Combinatorial chemistry & high throughput screening, 2015-01, Vol.18 (1), p.53

2015

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A highly efficient bismuth salts-catalyzed route for the synthesis of α-aminophosphonates

Molecules (Basel, Switzerland), 2010-11, Vol.15 (11), p.8205-8213

2010

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Potential Effects of Iodine Supplementation on Inflammatory Processes and Toxin Removal Following COVID-19 Vaccination

Biological trace element research, 2022-09, Vol.200 (9), p.3941-3944

2022

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Remarkable iodine-catalyzed synthesis of novel pyrrole-bearing N-polyaromatic beta-lactams

Molecules (Basel, Switzerland), 2010-02, Vol.15 (2), p.1082-1088

2010

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Bismuth nitrate-induced novel nitration of estradiol: An entry to new anticancer agents

European journal of medicinal chemistry, 2014-07, Vol.82, p.574-583

2014

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Asymmetric synthesis of anticancer β-lactams via Staudinger reaction: Utilization of chiral ketene from carbohydrate

European journal of medicinal chemistry, 2010-02, Vol.45 (2), p.846-848

2010

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On the Stereodivergent Behavior Observed in the Staudinger Reaction between Methoxyketene and (E)-N-Benzylidenearyl Amines

Angewandte Chemie (International ed.), 2007-01, Vol.46 (17), p.3028-3032

2007

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Simple Synthesis of Substituted Pyrroles

Journal of organic chemistry, 2004-01, Vol.69 (1), p.213-216

2004

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Ultrasound-assisted bismuth nitrate-induced green synthesis of novel pyrrole derivatives and their biological evaluation as anticancer agents

European journal of medicinal chemistry, 2012-04, Vol.50, p.209-215

2012

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Ultrasound-assisted aza-Michael reaction in water: A green procedure

Ultrasonics sonochemistry, 2012-07, Vol.19 (4), p.969-973

2012

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Role of imine isomerization in the stereocontrol of the Staudinger reaction between ketenes and imines

RSC advances, 2021-12, Vol.12 (1), p.14-117

2021

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A green, chemoselective, and practical approach toward N-(2-azetidinonyl) 2,5-disubstituted pyrroles

RSC advances, 2013-01, Vol.3 (37), p.16756-16764

2013

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Advances in Microwave Chemistry

Metal‐Free Cross‐Dehydrogenative Coupling (CDC): Molecular Iodine as a Versatile Catalyst/Reagent for CDC Reactions

Bismuth Nitrate-Catalyzed Versatile Michael Reactions

Synthesis of Medicinally Privileged Heterocycles through Dielectric Heating

Drug Repurposing Strategy (DRS): Emerging Approach to Identify Potential Therapeutics for Treatment of Novel Coronavirus Infection

Beta-Lactams: Novel Synthetic Pathways and Applications

A microwave-assisted bismuth nitrate-catalyzed unique route toward 1,4-dihydropyridines

Advances in Hydrogen Production from Natural Gas Reforming

Microwave-induced Bismuth Salts-mediated Synthesis of Molecules of Medicinal Interests

An expeditious iodine-catalyzed synthesis of 3-pyrrole-substituted 2-azetidinones

Polysaccharides from Dolichos biflorus Linn and Trachyspermum ammi Linn seeds: isolation, characterization and remarkable antimicrobial activity

An expeditious synthesis of N-substituted pyrroles via microwave-induced iodine-catalyzed reactions under solventless conditions

Green Approaches in Medicinal Chemistry for Sustainable Drug Design

A selective, expeditious and sustainable entry en route to benzopyrazines and bis-benzopyrazines

A highly efficient bismuth salts-catalyzed route for the synthesis of α-aminophosphonates

Potential Effects of Iodine Supplementation on Inflammatory Processes and Toxin Removal Following COVID-19 Vaccination

Remarkable iodine-catalyzed synthesis of novel pyrrole-bearing N-polyaromatic beta-lactams

Bismuth nitrate-induced novel nitration of estradiol: An entry to new anticancer agents

Asymmetric synthesis of anticancer β-lactams via Staudinger reaction: Utilization of chiral ketene from carbohydrate

On the Stereodivergent Behavior Observed in the Staudinger Reaction between Methoxyketene and (E)-N-Benzylidenearyl Amines

Simple Synthesis of Substituted Pyrroles

Ultrasound-assisted bismuth nitrate-induced green synthesis of novel pyrrole derivatives and their biological evaluation as anticancer agents

Ultrasound-assisted aza-Michael reaction in water: A green procedure

Role of imine isomerization in the stereocontrol of the Staudinger reaction between ketenes and imines

A green, chemoselective, and practical approach toward N-(2-azetidinonyl) 2,5-disubstituted pyrroles

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