1,3-Dipolar Addition of Phenylazide to the Carbon−Carbon Double Bond: An ab Initio Study
Author:
Affiliation:
1. Department of Chemistry and Center for Biomolecular Simulation, Columbia University, 3000 Broadway, New York, New York 10027
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp9839403
Reference27 articles.
1. Theory of Substituent Effects on Pericyclic Reaction Rates: Alkoxy Substituents in the Claisen Rearrangement
2. Accelerated Racemization of Aspartic Acid and Asparagine Residues via Succinimide Intermediates: An ab Initio Theoretical Exploration of Mechanism
3. Synchronous or Asynchronous? An “Experimental” Transition State from a Direct Comparison of Experimental and Theoretical Kinetic Isotope Effects for a Diels−Alder Reaction
4. Theoretical Study of a Termolecular Mechanism for the Reaction of (Trimethylsilyl)thiazole with Carbonyl Compounds
5. Stabilization of the Transition State of the Chorismate-Prephenate Rearrangement: An ab Initio Study of Enzyme and Antibody Catalysis
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