EPR observation of cathodically-generated radical anions of colchicides and isocolchicides, and a comparison with the radical anions of troponoids. A general rationalization of the spin-density distribution in these systems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Colchicine red-ox chemistry revisited: Cathodic behavior and EPR observation of an intermediate radical anion
2. Orientation in nucleophilic substitution at the cycloheptatrienone nucleus: failure of predictions from either electron spin resonance data or molecular orbital treatments
3. Radical paths in the decay of 2- and 3-halotropone radical anions
4. Competition between base addition and electron transfer in unsaturated systems: the case of 3-methoxytropone
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1. Electrochemical Site‐Selective Alkylation of Tropones via Formal C(sp3)−C(sp2) Coupling Reaction;Advanced Synthesis & Catalysis;2024-03-27
2. MECHANISTIC STUDY OF COLCHICINE’s ELECTROCHEMICAL OXIDATION;Electrochimica Acta;2015-10
3. Mechanistic study of colchicine's reduction behavior;Electrochemistry Communications;2015-07
4. β-Phenylethylamines and the isoquinoline alkaloids;Nat. Prod. Rep.;2004
5. Tautomeric selectivity towards colchicinoids in the tosylation of colchiceine on a heterogeneous, easily removable catalyst;Organic & Biomolecular Chemistry;2003
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