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Browsing School of Chemical Sciences by Title

Browsing School of Chemical Sciences by Title

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  • Narvekar, K.U.; Srinivasan, B.R. (IUCrData. 5(1); 2020; ArticleID_x200100.)
  • Shaikh, S.A.L.; Mendhe, A.C.; Nadimetla, D.N.; Biradar, M.R.; Vijayanand, P.; Puyad, A.L.; Sankapal, B.R.; Bhosale, Sidhanath V.; Bhosale, S.V. (Journal of Photochemistry & Photobiology, A: Chemistry. 447; 2024; ArticleID_115220.)
    Although dye sensitized solar cell (DSSC) make promising progress for solar energy conversion to electrical energy, there are still great need for further research work to develop an efficient sensitizer with a simple ...
  • Majik, M.S. (Letters in Organic Chemistry. 14(3); 2017; 147-152.)
    Pyrrolidine-based ring systems are ubiquitous in nature. (R)-Bgugaine is a 2-alkylated pyrrolidine alkaloid which has been isolated from the tubers of Arisarum vulgare, a toxic Araceae found along the Mediterranean coast. ...
  • Singh, K.S.; Majik, M.S. (Marine Sponges: Chemicobiological and Biomedical Applications, Ed. by: Ramjee Pallela and Hermann Ehrlich. Springer. 2016; 257-286.)
    Marine sponges are considered to be a rich source of biologically active secondary metabolites with unique and diverse chemical structures. They constitute nearly one third of the secondary metabolites isolated from marine ...
  • Parvatkar, P.T.; Tilve, S.G. (Bioactive Heterocycles: Synthesis and Biological Evaluation, Ed. by: K.L. Ameta, R.P. Pawar and A.J. Domb. Biochemistry Research Trends. Nova Science Publishers, New York. 2012; 217-233.)
    Tetracyclic heteroaromatic compounds with linear or angularly fused indoloquinoline ring systems constitute an important structural moiety in natural products. The indoloquinoline alkaloids cryptolepine, isocryptolepine ...
  • Majithia, M.; Barretto, D.A. (Advances in Nano and Biochemistry: Environmental and Biomedical Applications, Ed. by Pranay Morajkar, Milind Naik. 2023; 285-367.)
    Green synthesis of nanoparticles (NPs) refers to an approach of nanoparticle production that uses living entities such as bacteria, fungi, and plants as a replacement to harmful chemicals for yielding NPs. The process of ...
  • D'Souza, A.M.; Paknikar, S.K.; Dev, V.; Beauchamp, P.S.; Kamat, S.P. (Journal of Natural Products. 67(4); 2004; 700-702.)
    A biogenetic-type synthesis of (+)-cymbodiacetal (1), a novel bismonoterpenoid dihemiacetal, is described.
  • Fondekar, K.P.P.; Paknikar, S.K.; Torres, S.; Kamat, S.P. (Natural Product Communications. 7(7); 2012; 827-830.)
    A biogenetic-type synthesis of 2-hydroxy-4,4,7-trimethyl-1(4H)-naphthalenone (1), a modified apocarotenoid isolated from Ipomoea pes-caprae (Linn.) R.Br. showing anti-inflammatory activity by inhibiting prostaglandin ...
  • Paknikar, S.K.; Naik, C.G.; Ramanamma, C.V. (Journal of the Indian Chemical Society. 75(10-12); 1998; 729-733.)
    A hypothetical biosynthetic pathway for the conversion of farnesylpyrophosphate into seaquichamaenol 1, a modified sesquiterpenoid isolated from Chaemaecyparis formosensis Matsum is proposed. The synthesis of 1 which lends ...
  • Singh, G.; Lakhi, K.S.; Sil, S.; Bhosale, S.V.; Kim, I-Y.; Albahily, K.; Vinu, A. (Carbon. 148; 2019; 164-186.)
    The quest for producing cost-effective and efficient adsorbents for CO sub(2) capture has received enormous attention in recent times. Biomass-derived porous carbons are considered to be the most preferred adsorbent materials ...
  • Paknikar, S.K.; Petel, J. (Chemistry and Industry (London). 1988; 530-531.)
  • Chen, J.; Kadam, G.; Gupta, A.; Anuradha; Bhosale, S.V.; Zheng, F.; Zhou, C-H.; Jia, B-H.; Dalal, D.S.; Li, J. (Chemistry - A European Journal. 24(55); 2018; 14668-14678.)
    Supramolecular assembly of chromophores with inherent resistance to aggregation-induced self-quenching is significant to applications such as chemical sensing and organic light emitting diodes (OLEDs). In this work, molecular ...
  • Paknikar, S.K.; Fondekar, K.P.; Mayer, R. (Natural Product Letters. 8(4); 1996; 253-256.)
    Biomimetic synthesis of (-)-tanzanene (1) from (-)-alloaromadendrene (4) is reported. This first synthesis of (-)-tanzanene also established its absolute configuration as shown in 1.
  • Praveen, P.J.; Parameswaran, P.S.; Majik, M.S. (Synthesis. 47(13); 2015; 1827-1837.)
    Bis(indolyl)methane (BIM) alkaloids are an important group of bioactive natural products predominantly found in marine organisms. Thus, compounds like arsindoline A and B, vibrindole A, arundine, and trisindoline are found ...
  • Srinivasan, B.R.; Naether, C.; Naik, A.R.; Bensch, W. (Acta Crystallographica Section E-Structure Reports Online. 64(1); 2008; M66-M67.)
    The title compound, (C3H10N)(2)[MoS4], was synthesized by passing a rapid stream of H2S into an aqueous isopropylamine solution of molybdic acid. The title compound is isotypic with the corresponding W analogue (C3H10N)(2)[WS4]; ...
  • Srinivasan, B.R.; Naether, C.; Bensch, W. (Acta Crystallographica Section E-Structure Reports Online. 64; 2008; M296-M297.)
  • Srinivasan, B.R.; Naik, A.R.; Poisot, M.; Naether, C.; Bensch, W. (Polyhedron. 28(7); 2009; 1379-1385.)
    The organic tetrasulfidometalates (pipH)(2)[MS(4)] (pipH = piperazin-1-ium; M = W 1; M = Mo 2) were prepared by a mechanical grinding of solid (NH(4))(2)[MS(4)] (M = Mo or W) with the cyclic diamine piperazine (pip). ...
  • Srinivasan, B.R.; Naether, C.; Bensch, W. (Acta Crystallographica Section C-Crystal Structure Communications. 62; 2006; M98-M101.)
    The structures of the title complexes, (C6H15N2)2[MoS4], (I), and (C6H16N2)[MoS4], (II), can be described as consisting of discrete tetra-hedral [MoS4]2- dianions that are linked to the organic ammonium cations via weak ...
  • Srinivasan, B.R.; Girkar, S.V.; Raghavaiah, P. (Acta Crystallographica Section E-Structure Reports Online. 63; 2007; M3100-M3101.)
    The title compound, (C8H12N)(2)[WS4], was synthesized by the aqueous reaction of ammonium tetrasulfidotungstate(VI) with benzyl( methyl) amine in a 1:2 molar ratio.The compound is isotypic with the corresponding Mo analogue, ...
  • Srinivasan, B.R.; Girkar, S.V.; Raghavaiah, P. (Acta Crystallographica Section E-Structure Reports Online. 63; 2007; M2737-M2738.)
    The title compound, (C8H12N)(2)[MoS4], was synthesized by the aqueous reaction of ammonium tetrathiomolybdate with benzyl(methyl) amine in a 1:2 molar ratio. The structure consists of a slightly distorted tetrahedral ...

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