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E. Kwan Lecture 33: N-Heterocyclic Carbines N-Heterocyclic Carbines Eugene E. Kwan November 22, 2010. Mes Cl Mes Chem 106 Helpful References 1. N-HeterocycliCarbineses as Organocatalysts. Marion,

J.; Pfeifer, A.L.; Led, T. J. Am. Chem. Soc. 2010, 134, 16. N 4. Positron Emission Tomography: A New Approach to Chemical and Biological Analysis. J. Cornfield, R. T. A Chem. Eng. 2007, 49, 841-849. (physics and chemistry of biological material) P 5. nuclear Magnetic Resonance Spectroscopy(NMR) of Carbine.” Boreas, A.; Fie big, J.A. J. Am. Chem. Soc. 2006, 121, 9. (Physics) N 6. †Cobalt-Catalyzed Synthesis of Carbonyl Nitro ne.” Boreas, A.; Belonged, E. R. J. Am. Chem. Soc. 2008, 123, 3. (Physics) N 7. catalytic Synthesis of N-Heterocyclic Carbines: A Tertiary Catalyst.” Boreas, A.J.; Belonged, E.R.; Jaggard, J.-F.; Sarto, M.J. J. Am. Chem. Soc. 2008, 123, 4. (physics and chemistry from the second-generation carbine catalyst) P 8. carbon Monoxide-Catalyzed Hydrazine Synthesis.” Boreas, A.J. J. Am. Chem. Soc. 1994, 116, 4. (Physics) Back to Top 9.6. Theoretical Approaches to Carbine Catalysis. 9.6.1. Efficient AzaB-Catalyzed Synthesis of Carbene. Efficient AzaB-catalyzed carbine synthesis has been reported in two papers: one as a catalyst for the hydrothermal-substrate annealing of an organic-based Ankeny precursor, and the other for the reaction between an Ankeny precursor and cycloalkanes.

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