Computational studies on formation and intermolecular [1+2] cycloadditions of nitrilimines
2,5-disubstituted tetrazoles decompose thermally to give nitrilimines (R1–CNN–R2), whose electronic structure widely varies with the substituents R1 and R2. In particular, for R1, R2 = H, the carbenic contribution to the resonance structure is small, while for NH2-disubstitution Natural Resonance Th...
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2012
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| Online Access: | http://spectrum.library.concordia.ca/975016/1/Mehrpajouh_MSc_2012.pdf Mehrpajouh, Sima <http://spectrum.library.concordia.ca/view/creators/Mehrpajouh=3ASima=3A=3A.html> (2012) Computational studies on formation and intermolecular [1+2] cycloadditions of nitrilimines. Masters thesis, Concordia University. |
Internet
http://spectrum.library.concordia.ca/975016/1/Mehrpajouh_MSc_2012.pdfMehrpajouh, Sima <http://spectrum.library.concordia.ca/view/creators/Mehrpajouh=3ASima=3A=3A.html> (2012) Computational studies on formation and intermolecular [1+2] cycloadditions of nitrilimines. Masters thesis, Concordia University.