Vijayendran Gowri

Employment

• Institute of Nano Science and Technology
  2018 - Present

Education

• Indian Institute of Science
  2005 - 2011
• University of Madras
  2003 - 2005

Projects & Funding

Projects & funding information is unavailable.

Publications (11)

• Tuning of the Cross-Glaser Products mediated by Substrate-Catalyst’s Polymeric Backbone Interactions
  Chemical Communications 2020 DOI: 10.1039/c9cc08565c
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• Designing of Push–Pull Chromophores with Tunable Electronic and Luminescent Properties Using Urea as the Electron Donor
  The Journal of Organic Chemistry 2019 DOI: 10.1021/acs.joc.9b00841
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• Design and Synthesis of Aviram-Ratner-Type Dyads and Rectification Studies in Langmuir-Blodgett (LB) Films
  Chemistry - A European Journal 2016 DOI: 10.1002/chem.201505216
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• ChemInform Abstract: An Enantiospecific Synthesis of a Crinipellin.
  ChemInform 2012 DOI: 10.1002/chin.201229202
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• Enantiospecific total synthesis of 15-hydroxy-5-(methoxymethoxy)crinipellin-9-one
  Tetrahedron 2012 DOI: 10.1016/j.tet.2012.02.018
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• An Enantiospecific Approach to Tetraquinane Diterpenes Crinipellins: Synthesis of Norcrinipellins
  Synlett 2011 DOI: 10.1055/s-0031-1289533
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• Enantiospecific synthesis of angular triquinanes
  Tetrahedron: Asymmetry 2011 DOI: 10.1016/j.tetasy.2011.08.016
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• Enantioselective syntheses of diquinane and (cis, anti, cis)-linear triquinanes
  Tetrahedron: Asymmetry 2010 DOI: 10.1016/j.tetasy.2010.01.014
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• ChemInform Abstract: Enantiospecific Approach to the Tricyclic Core Structure (IV) of Tricycloillicinone (V), Ialibinones, and Takaneones via Ring-Closing Metathesis Reaction.
  ChemInform 2009 DOI: 10.1002/chin.200929182
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• Enantiospecific approach to the tricyclic core structure of tricycloillicinone, ialibinones, and takaneones via ring-closing metathesis reaction
  Tetrahedron 2009 DOI: 10.1016/j.tet.2009.01.096
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