Computational Insight into the Carbenic Character of Nitrilimines from a Reactivity Perspective
Author:
Affiliation:
1. Centre for Research in Molecular Modeling and Department of Chemistry and Biochemistry, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec, Canada H4B 1R6
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp208510d
Reference55 articles.
1. 1,3-Dipolar Cycloadditions. Past and Future
2. Stereochemical aspects of the intramolecular 1,1-cycloaddition reaction of nitrilimines
3. Hartree-Fock descriptions of 1,3-dipoles. Zwitterions, 1,3-diradicals, or hypervalent species?
4. Structure of nitrilimine: allenic or propargylic?
5. Sharp, J. T. In The Chemistry of Heterocyclic Compounds 59: Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products;Padwa, A.; Pearson, W. H., Eds.John Wiley and Sons:New York, 2002; pp473–537.
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