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Aryltriazenes as Coupling Partners in the Hiyama, Hiyama‐Suzuki and Hiyama‐Heck Cross‐Coupling Reactions Using Conventional and Ionic Liquid Reagents and Solvents

European journal of organic chemistry, 2022-12, Vol.2022 (45), p.n/a

2022

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Libraries of C‐5 Substituted Imidazoles and Oxazoles by Sequential Van Leusen (VL)–Suzuki, VL–Heck and VL–Sonogashira in Imidazolium‐ILs with Piperidine‐Appended‐IL as Base

European journal of organic chemistry, 2018-10, Vol.2018 (38), p.5285-5288

2018

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Highly Efficient Synthesis of 1,3-Dioxanes via Prins Reaction in Brønsted-Acidic Imidazolium Ionic Liquid

Synthetic communications, 2014-03, Vol.44 (6), p.762-771

2014

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Facile Access to Diverse Libraries of Internal Alkynes via Sequential Iododediazoniation/Decarboxylative Sonogashira Reaction in Imidazolium ILs without Ligand or Additive

European journal of organic chemistry, 2019-03, Vol.2019 (10), p.2061-2064

2019

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Piperidine-appended imidazolium ionic liquid as task-specific basic-IL for Suzuki and Heck reactions and for tandem Wittig-Suzuki, Wittig-Heck, Horner-Emmons-Suzuki, and Horner-Emmons-Heck protocols

Applied catalysis. A, General, 2017-08, Vol.543, p.150-161

2017

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Highly efficient synthesis of amides via Ritter chemistry with ionic liquids

Tetrahedron letters, 2011-02, Vol.52 (8), p.867-871

2011

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1‐Aryltriazenes in the Suzuki, Heck, and Sonogashira Reactions in Imidazolium‐ILs, with [BMIM(SO3H)][OTf] or Sc(OTf)3 as Promoter, and Pd(OAc)2 or NiCl2·glyme as Catalyst

European journal of organic chemistry, 2019-09, Vol.2019 (35), p.6088-6093

2019

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Arenediazonium salts immobilized in imidazolium ionic liquids as electrophilic partners in the Pd(OAc) 2-catalyzed Matsuda–Heck arylation

Tetrahedron letters, 2011-04, Vol.52 (15), p.1733-1737

2011

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Pd(OAc) 2-catalyzed cross-coupling of polyfluoroarenes with simple aromatics in imidazolium ionic liquids (ILs) without oxidant and additive and with recycling/reuse of the IL

Tetrahedron letters, 2011-10, Vol.52 (42), p.5525-5529

2011

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Highly efficient synthesis of amides from ketoximes using trifluoromethanesulphonic anhydride

RSC advances, 2015-01, Vol.5 (74), p.60106-60113

2015

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In vitro antimicrobial combat, molecular modelling and structure activity relationship studies of novel class of aryl-ethyne tethered coumarin analogues and some 3-aryl coumarin derivatives

European journal of medicinal chemistry reports, 2022-08, Vol.5, p.100048, Article 100048

2022

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Triflic Anhydride: A Mild Reagent for Highly Efficient Synthesis of 1,2-Benzisoxazoles, Isoxazolo, and Isothiazolo Quinolines Without Additive or Base

Synthetic communications, 2014-02, Vol.44 (4), p.547-555

2014

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Pd-catalysed one-pot and three-component sequential chemoselective double cross-coupling: Synthesis of novel 2-aryl-1,3-azoles from 4-bromophenyl tosylate

Tetrahedron Green Chem, 2024-12, Vol.4, p.100051, Article 100051

2024

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(Z)-Ethyl 2-cyano-3-(1H-imidazol-2-yl)acrylate

Acta crystallographica. Section E, Structure reports online, 2013-08, Vol.69 (Pt 8), p.o1223-o1223

2013

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Ionic liquid Mediated Pd-catalyzed sonochemistry for facile synthesis of carbazoles: Molecular Modelling and antimicrobial studies

Tetrahedron Green Chem, 2024-06, Vol.3, p.100038, Article 100038

2024

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(E)-Ethyl 2-cyano-3-(furan-2-yl)acrylate

Acta crystallographica. Section E, Structure reports online, 2012-05, Vol.68 (Pt 5), p.o1482-o1482

2012

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Reaction of triflyl-imidazole with aldoximes: facile synthesis of nitriles and formation of novel aldoxime-bis( N-triflyl)-imidazole adducts

Tetrahedron letters, 2011-10, Vol.52 (40), p.5184-5187

2011

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In silico molecular docking and In vitro antimicrobial evaluation of some C5-substituted imidazole analogues

European journal of medicinal chemistry reports, 2021-12, Vol.3, p.100015, Article 100015

2021

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Synthesis and biological activities of some new fluorinated coumarins and 1-aza coumarins

European journal of medicinal chemistry, 2008-10, Vol.43 (10), p.2178-2188

2008

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N-(2-Chloro-quinolin-3-ylmethyl-ene)aniline

Acta crystallographica. Section E, Structure reports online, 2008-01, Vol.64 (Pt 1), p.o258-o258

2008

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A Facile One Pot Synthesis of New Tricyclic Coumarins from Single Synthon [1

Journal of heterocyclic chemistry, 2013-09, Vol.50 (5), p.1014-1020

2013

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Crystal Structure of 7-Methyl-4-[(4′-fluoro)anilinomethyl]coumarin

Analytical Sciences: X-ray Structure Analysis Online, 2007, Vol.23, pp.x31-x32

2007

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Synthesis, Characterization, and Antimicrobial Studies of Novel Benzodipyran Analog of Chloramphenicol

Journal of heterocyclic chemistry, 2013-09, Vol.50 (5), p.1108-1115

2013

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N-ethyltetramethylguanidinium ionic liquid [ETMG][EtSO3] as organocatalyst and solvent for facile amide synthesis by formyl-transfer with N-formyl-saccharin

Tetrahedron letters, 2022-08, Vol.104, p.153990, Article 153990

2022

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Pd(OAc)2 catalyzed synthesis of 2-aryl- and 2-heteroaryl-benzoxazoles and benzothiazoles in imidazolium ionic liquids (ILs) without additives and with recycling/reuse of the IL

Tetrahedron letters, 2012-08, Vol.53 (32), p.4212-4215

2012

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Aryltriazenes as Coupling Partners in the Hiyama, Hiyama‐Suzuki and Hiyama‐Heck Cross‐Coupling Reactions Using Conventional and Ionic Liquid Reagents and Solvents

Libraries of C‐5 Substituted Imidazoles and Oxazoles by Sequential Van Leusen (VL)–Suzuki, VL–Heck and VL–Sonogashira in Imidazolium‐ILs with Piperidine‐Appended‐IL as Base

Highly Efficient Synthesis of 1,3-Dioxanes via Prins Reaction in Brønsted-Acidic Imidazolium Ionic Liquid

Facile Access to Diverse Libraries of Internal Alkynes via Sequential Iododediazoniation/Decarboxylative Sonogashira Reaction in Imidazolium ILs without Ligand or Additive

Piperidine-appended imidazolium ionic liquid as task-specific basic-IL for Suzuki and Heck reactions and for tandem Wittig-Suzuki, Wittig-Heck, Horner-Emmons-Suzuki, and Horner-Emmons-Heck protocols

Highly efficient synthesis of amides via Ritter chemistry with ionic liquids

1‐Aryltriazenes in the Suzuki, Heck, and Sonogashira Reactions in Imidazolium‐ILs, with [BMIM(SO3H)][OTf] or Sc(OTf)3 as Promoter, and Pd(OAc)2 or NiCl2·glyme as Catalyst

Arenediazonium salts immobilized in imidazolium ionic liquids as electrophilic partners in the Pd(OAc) 2-catalyzed Matsuda–Heck arylation

Pd(OAc) 2-catalyzed cross-coupling of polyfluoroarenes with simple aromatics in imidazolium ionic liquids (ILs) without oxidant and additive and with recycling/reuse of the IL

Highly efficient synthesis of amides from ketoximes using trifluoromethanesulphonic anhydride

In vitro antimicrobial combat, molecular modelling and structure activity relationship studies of novel class of aryl-ethyne tethered coumarin analogues and some 3-aryl coumarin derivatives

Triflic Anhydride: A Mild Reagent for Highly Efficient Synthesis of 1,2-Benzisoxazoles, Isoxazolo, and Isothiazolo Quinolines Without Additive or Base

Pd-catalysed one-pot and three-component sequential chemoselective double cross-coupling: Synthesis of novel 2-aryl-1,3-azoles from 4-bromophenyl tosylate

(Z)-Ethyl 2-cyano-3-(1H-imidazol-2-yl)acrylate

Ionic liquid Mediated Pd-catalyzed sonochemistry for facile synthesis of carbazoles: Molecular Modelling and antimicrobial studies

(E)-Ethyl 2-cyano-3-(furan-2-yl)acrylate

Reaction of triflyl-imidazole with aldoximes: facile synthesis of nitriles and formation of novel aldoxime-bis( N-triflyl)-imidazole adducts

In silico molecular docking and In vitro antimicrobial evaluation of some C5-substituted imidazole analogues

Synthesis and biological activities of some new fluorinated coumarins and 1-aza coumarins

N-(2-Chloro-quinolin-3-ylmethyl-ene)aniline

A Facile One Pot Synthesis of New Tricyclic Coumarins from Single Synthon [1

Crystal Structure of 7-Methyl-4-[(4′-fluoro)anilinomethyl]coumarin

Synthesis, Characterization, and Antimicrobial Studies of Novel Benzodipyran Analog of Chloramphenicol

N-ethyltetramethylguanidinium ionic liquid [ETMG][EtSO3] as organocatalyst and solvent for facile amide synthesis by formyl-transfer with N-formyl-saccharin

Pd(OAc)2 catalyzed synthesis of 2-aryl- and 2-heteroaryl-benzoxazoles and benzothiazoles in imidazolium ionic liquids (ILs) without additives and with recycling/reuse of the IL

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