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Proline and its Derivatives as Organocatalysts for Multi‐ Component Reactions in Aqueous Media: Synergic Pathways to the Green Synthesis of Heterocycles

Advanced synthesis & catalysis, 2020-01, Vol.362 (1), p.87-110

2020

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Discovery of Antimycobacterial Spiro-piperidin-4-ones: An Atom Economic, Stereoselective Synthesis, and Biological Intervention

Journal of medicinal chemistry, 2008-09, Vol.51 (18), p.5731-5735

2008

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A facile synthesis and antimycobacterial evaluation of novel spiro-pyrido-pyrrolizines and pyrrolidines

European journal of medicinal chemistry, 2009-09, Vol.44 (9), p.3821-3829

2009

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An atom efficient, solvent-free, green synthesis and antimycobacterial evaluation of 2-amino-6-methyl-4-aryl-8-[(E)-arylmethylidene]-5,6,7,8 -tetrahydro -4H -pyrano [3,2 -c ]pyridine -3 -carbonitriles

Bioorganic & medicinal chemistry, 2007-12, Vol.17 (23), p.6459-6462

2007

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Antimycobacterial activity of spirooxindolo-pyrrolidine, pyrrolizine and pyrrolothiazole hybrids obtained by a three-component regio- and stereoselective 1,3-dipolar cycloaddition

MedChemComm, 2011-07, Vol.2 (7), p.626

2011

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An eco-friendly three-component regio- and stereoselective synthesis of highly functionalized dihydroindeno[1,2-b]pyrroles under grinding

Green chemistry : an international journal and green chemistry resource : GC, 2014-01, Vol.16 (3), p.1297-1304

2014

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A highly atom economic, chemo-, regio- and stereoselective synthesis and evaluation of spiro-pyrrolothiazoles as antitubercular agents

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (1), p.350-353

2010

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New four-component reactions in water: a convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,4′-pyrazolo[3,4- b]pyridine derivatives

Tetrahedron, 2011-05, Vol.67 (18), p.3201-3208

2011

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A microwave-assisted facile regioselective Fischer indole synthesis and antitubercular evaluation of novel 2-aryl-3,4-dihydro-2H-thieno[3,2-b]indoles

Bioorganic & medicinal chemistry letters, 2009-06, Vol.19 (11), p.3006-3009

2009

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A highly atom economic, chemo-, regio- and stereoselective synthesis, and discovery of spiro-pyrido-pyrrolizines and pyrrolidines as antimycobacterial agents

Tetrahedron, 2008-03, Vol.64 (13), p.2962-2971

2008

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An atom economic synthesis and antitubercular evaluation of novel spiro-cyclohexanones

Bioorganic & medicinal chemistry letters, 2009-07, Vol.19 (13), p.3461-3465

2009

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A facile domino protocol for the regioselective synthesis and discovery of novel 2-amino-5-arylthieno-[2,3- b]thiophenes as antimycobacterial agents

Tetrahedron letters, 2009-11, Vol.50 (45), p.6191-6195

2009

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Facile four-component domino reactions for the synthesis of highly functionalized tetrahydroquinolones

Tetrahedron letters, 2013-09, Vol.54 (39), p.5302-5306

2013

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Facile four-component domino reactions for the synthesis of 2,6-diaryl-4-(1H-indol-3-yl)-3-cyanopyridines

Tetrahedron letters, 2014-10, Vol.55 (40), p.5486-5490

2014

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Aryl Grignard Reagents in Chemodivergent N- and C-Arylations: Concise Access to Two Families of Tetracyclic Fused Carbazoles from 6-Nitroquinolines

European journal of organic chemistry, 2012-04, Vol.2012 (12), p.2375-2385

2012

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A facile four-component tandem protocol for the synthesis of novel 2,6-diaryl-2,3-dihydro-1H-pyridin-4-ones

Tetrahedron letters, 2007-08, Vol.48 (32), p.5627-5629

2007

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Synthesis, Stereochemistry, and Antimicrobial Activity of 2,6-Diaryl-3-(arylthio)piperidin-4-ones

Chemical and Pharmaceutical Bulletin, 2006, Vol.54(6), pp.795-801

2006

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A regio- and stereoselective 1,3-dipolar cycloaddition for the synthesis of novel spiro-pyrrolothiazolyloxindoles and their antitubercular evaluation

European journal of medicinal chemistry, 2010-12, Vol.45 (12), p.5653-5661

2010

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A tandem multi-component synthesis of 5,7-diaryl-5,6,7,8-tetrahydro-1H-pyrido[3,4-b][1,4]thiazin-2(3H)-ones

Tetrahedron, 2006-05, Vol.62 (20), p.4892-4899

2006

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Crystal structure of 2-(2-bromophenyl)-4-(1 H -indol-3-yl)-6-(thiophen-2-yl)pyridine-3-carbonitrile

Acta crystallographica. Section E, Structure reports online, 2014-09, Vol.70 (9), p.o968-o969

2014

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A catalyst-free multicomponent domino sequence for the diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-(arylamino)allyl]chromen-4-ones

Beilstein journal of organic chemistry, 2014-02, Vol.10 (1), p.459-465

2014

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Crystal structure of 2-(4-chlorophenyl)-4-(1 H -indol-3-yl)-6-phenylpyridine-3-carbonitrile

Acta crystallographica. Section E, Structure reports online, 2014-09, Vol.70 (9), p.o978-o978

2014

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Crystal structures of two 2,9-dithia-13-azadispiro[4.1.4 7 .3 5 ]tetradecan-6-ones

Acta crystallographica. Section E, Crystallographic communications, 2015, Vol.71 (12), p.1516-1520

2015

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A facile regio- and stereoselective synthesis of trans-ethyl 5-aroyl-4-aryl-2-[(arylsulfonyl)methyl]-4,5-dihydrofuran-3-carboxylates

ARKIVOC, 2013-07, Vol.2013 (4), p.1-14

2013

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A Facile Synthesis and Discovery of Highly Functionalized Tetrahydro-pyridines and Pyridines as Antimycobacterial Agents

Chemical and Pharmaceutical Bulletin, 2010/05/01, Vol.58(5), pp.602-610

2010

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Proline and its Derivatives as Organocatalysts for Multi‐ Component Reactions in Aqueous Media: Synergic Pathways to the Green Synthesis of Heterocycles

Discovery of Antimycobacterial Spiro-piperidin-4-ones: An Atom Economic, Stereoselective Synthesis, and Biological Intervention

A facile synthesis and antimycobacterial evaluation of novel spiro-pyrido-pyrrolizines and pyrrolidines

An atom efficient, solvent-free, green synthesis and antimycobacterial evaluation of 2-amino-6-methyl-4-aryl-8-[(E)-arylmethylidene]-5,6,7,8 -tetrahydro -4H -pyrano [3,2 -c ]pyridine -3 -carbonitriles

Antimycobacterial activity of spirooxindolo-pyrrolidine, pyrrolizine and pyrrolothiazole hybrids obtained by a three-component regio- and stereoselective 1,3-dipolar cycloaddition

An eco-friendly three-component regio- and stereoselective synthesis of highly functionalized dihydroindeno[1,2-b]pyrroles under grinding

A highly atom economic, chemo-, regio- and stereoselective synthesis and evaluation of spiro-pyrrolothiazoles as antitubercular agents

New four-component reactions in water: a convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,4′-pyrazolo[3,4- b]pyridine derivatives

A microwave-assisted facile regioselective Fischer indole synthesis and antitubercular evaluation of novel 2-aryl-3,4-dihydro-2H-thieno[3,2-b]indoles

A highly atom economic, chemo-, regio- and stereoselective synthesis, and discovery of spiro-pyrido-pyrrolizines and pyrrolidines as antimycobacterial agents

An atom economic synthesis and antitubercular evaluation of novel spiro-cyclohexanones

A facile domino protocol for the regioselective synthesis and discovery of novel 2-amino-5-arylthieno-[2,3- b]thiophenes as antimycobacterial agents

Facile four-component domino reactions for the synthesis of highly functionalized tetrahydroquinolones

Facile four-component domino reactions for the synthesis of 2,6-diaryl-4-(1H-indol-3-yl)-3-cyanopyridines

Aryl Grignard Reagents in Chemodivergent N- and C-Arylations: Concise Access to Two Families of Tetracyclic Fused Carbazoles from 6-Nitroquinolines

A facile four-component tandem protocol for the synthesis of novel 2,6-diaryl-2,3-dihydro-1H-pyridin-4-ones

Synthesis, Stereochemistry, and Antimicrobial Activity of 2,6-Diaryl-3-(arylthio)piperidin-4-ones

A regio- and stereoselective 1,3-dipolar cycloaddition for the synthesis of novel spiro-pyrrolothiazolyloxindoles and their antitubercular evaluation

A tandem multi-component synthesis of 5,7-diaryl-5,6,7,8-tetrahydro-1H-pyrido[3,4-b][1,4]thiazin-2(3H)-ones

Crystal structure of 2-(2-bromophenyl)-4-(1 H -indol-3-yl)-6-(thiophen-2-yl)pyridine-3-carbonitrile

A catalyst-free multicomponent domino sequence for the diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-(arylamino)allyl]chromen-4-ones

Crystal structure of 2-(4-chlorophenyl)-4-(1 H -indol-3-yl)-6-phenylpyridine-3-carbonitrile

Crystal structures of two 2,9-dithia-13-azadispiro[4.1.4 7 .3 5 ]tetradecan-6-ones

A facile regio- and stereoselective synthesis of trans-ethyl 5-aroyl-4-aryl-2-[(arylsulfonyl)methyl]-4,5-dihydrofuran-3-carboxylates

A Facile Synthesis and Discovery of Highly Functionalized Tetrahydro-pyridines and Pyridines as Antimycobacterial Agents

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