Publicacions en col·laboració amb investigadors/es de Madurai Kamaraj University (28)

2021

  1. Ionic liquid mediated synthesis and in vitro mechanistic exploration of polycyclic cage-like heterocyclic hybrid

    Journal of Heterocyclic Chemistry, Vol. 58, Núm. 2, pp. 580-588

2020

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

    Advanced Synthesis and Catalysis, Vol. 362, Núm. 1, pp. 87-110

2016

  1. A sustainable approach to the stereoselective synthesis of diazaheptacyclic cage systems based on a multicomponent strategy in an ionic liquid

    Molecules, Vol. 21, Núm. 2

  2. One-Pot Access to a Library of Dispiro Oxindole-pyrrolidine/pyrrolothiazole-thiochromane Hybrids via Three-Component 1,3-Dipolar Cycloaddition Reactions

    ACS Combinatorial Science, Vol. 18, Núm. 6, pp. 337-342

2015

  1. An efficient synthesis of N-substituted 3-nitrothiophen-2-amines

    Beilstein Journal of Organic Chemistry, Vol. 11, pp. 1707-1712

  2. Dipolar Cycloaddition-Based Multicomponent Reactions in Ionic Liquids: A Green, Fully Stereoselective Synthesis of Novel Polycyclic Cage Systems with the Generation of Two New Azaheterocyclic Rings

    Synthesis (Germany), Vol. 47, Núm. 18, pp. 2721-2730

  3. Straightforward synthesis of pyrrolo[3,4-b]quinolines through intramolecular Povarov reactions

    Tetrahedron Letters, Vol. 56, Núm. 49, pp. 6900-6903

2014

  1. 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, Vol. 10, pp. 459-465

  2. A heavy metal- and oxidant-free, one-pot synthesis of pyridines and fused pyridines based on a Lewis acid-catalyzed multicomponent reaction

    Chemical Communications, Vol. 50, Núm. 82, pp. 12270-12272

  3. Axial chirality of 4-arylpyrazolo[3,4- b ]pyridines. conformational analysis and absolute configuration

    Journal of Organic Chemistry, Vol. 79, Núm. 22, pp. 11039-11050

  4. Synthesis of heterocycles through multicomponent reactions in water

    Green Chemistry: Synthesis of Bioactive Heterocycles (Springer India), pp. 1-35

2013

  1. Chemodivergent, multicomponent domino reactions in aqueous media: L-proline-catalyzed assembly of densely functionalized 4H-pyrano[2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials

    Green Chemistry, Vol. 15, Núm. 5, pp. 1292-1299

  2. L-Proline catalysed domino reactions for the synthesis of heterocycles

    Current Organic Chemistry, Vol. 17, Núm. 18, pp. 2038-2064

2012

  1. 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, pp. 2375-2385

  2. Domino reactions in water: Diastereoselective synthesis of densely functionalized indolyldihydrofuran derivatives

    Green Chemistry, Vol. 14, Núm. 3, pp. 750-757

  3. Facile ionic liquid-mediated, three-component sequential reactions for the green, regio- and diastereoselective synthesis of furocoumarins

    Tetrahedron, Vol. 68, Núm. 27-28, pp. 5631-5636

2011

  1. A facile three-component [3+2]-cycloaddition/annulation domino protocol for the regio- and diastereoselective synthesis of novel penta- and hexacyclic cage systems, involving the generation of two heterocyclic rings and five contiguous stereocenters

    Tetrahedron, Vol. 67, Núm. 17, pp. 3132-3139

  2. A facile, three-component domino protocol for the microwave-assisted synthesis of functionalized naphtho[2,3-b]furan-4,9-diones in water

    Green Chemistry, Vol. 13, Núm. 8, pp. 2123-2129

  3. A three-component domino protocol for the facile synthesis of highly functionalized tetrahydroisoquinolines by creation of their benzene ring

    Tetrahedron, Vol. 67, Núm. 7, pp. 1432-1437

  4. Antimycobacterial activity of novel 1,2,4-oxadiazole-pyranopyridine/ chromene hybrids generated by chemoselective 1,3-dipolar cycloadditions of nitrile oxides

    Bioorganic and Medicinal Chemistry, Vol. 19, Núm. 11, pp. 3444-3450