Understanding the Formation of N−H Tautomers from α-Substituted Pyridines: Tautomerization of 2-Ethylpyridine Promoted by Osmium
Author:
Affiliation:
1. Departamento de Química Inorgánica, Instituto de Ciencia de Materiales de Aragón, Universidad de Zaragoza-CSIC, 50009 Zaragoza, Spain
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja073673r
Reference33 articles.
1. 172. The mechanism of decarboxylation. Part II. The production of cyanide-like ions from α-picolinic, quinaldinic, and isoquinaldinic acids
2. Observation of the Hammick Intermediate: Reduction of the Pyridine-2-ylid Ion in the Gas Phase
3. Iridium(III)-Induced Isomerization of 2-Substituted Pyridines to N-Heterocyclic Carbenes
4. Stabilization of NH Tautomers of Quinolines by Osmium and Ruthenium
5. Ruthenium Induced C−N Bond Activation of an N-Heterocyclic Carbene: Isolation of C- and N-Bound Tautomers
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