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Dr. R. K. Bansal

Emeritus Professor
Chemistry
THE IIS UNIVERSITY
India

Biography

Membership of the academic societies: Fellow Alexander von Humboldt Foundation, Bonn Life member, Indian Chemical Society Life member, Indian Science Congress Association Chemical Society Life member, Chemical Research Society of India Member Editorial Board of Phosphorus, Sulfur, Silicon & Related Elements

Research Interest

Structural Chemistry phytochemistry

Publications

  • Raj K. Bansal, N Gupta, S K Kumawat (2006) Origin of the Stereo- and Regioselectivities in the Diels-Alder Reactions of Azaphospholes: A DFT Investigation. Tetrahedron 62: 1548 .

  • Raj K. Bansal, N Gupta, S K Kumawat (2006) Diels-Alder Reactions of 5,6-Dihydrothiazolo[3,2-d][1,4,2]diazaphospholes: A DFT Investigation. Heteroat Chem 17: 402 .

  • Raj k. Bansal, N. Gupta, S. K. Kumawat, Z. Naturforsch (2007) Concerted and diradical stepwise mechanisms in the Diels-Alder reactions of phosphinine and phosphinine sulfide: A DFT investigation. 63b: 321.

  • Raj K. Bansal, N Gupta, S K Kumawat (2007) Recent Advances in the Chemistry of Anellated Azaphospholes. Curr Org Chem 11: 33.

  • RK Bansal, N Gupta, SK Kumawat G Dixit (2008) Diastereo- and regioselective Diels- alder reactions of 2-phosphaindolizines. Tetrahedron 64: 6395.

  • RK Bansal, SK Kumawat (2008) Diels- Alder reactions involving >C=P- functionality. Tetrahedron Report 64: 10945–10976 .

  • RK Bansal, N Gupta, G Dixit, SK Kumawat (2009) Theoretical investigation of an unusual sustituent effect on the dienophilicity of >C=P- functionality present in 2-phosphaindolizines. J Phys Org Chem 22: 125.

  • R.K. Bansal (2009) Annelated Azaphospholes. Topics in Heterocyclic Chemistry 20: 1-30.

  • N. Gupta, R. K. Bansal, M. von Hopffgarten, G. Frenking 1,5-Electrocyclization versus 1,5-proton shift in imidazolium allylides and 2-phosphaallylides. J Phys Org Chem.

  • R K Jangid, N. Gupta, R. K. Bansal, M. von Hopffgarten, G. Frenking (2011) Diels-Alder reaction of 2-phosphaindolizines catalyzed by organoaluminium reagent: theoretical and experimental results. Tetrahedron Lett. 52: 1721.

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