Corrins electrophilic reactions

Coproporphyrin I synthesis, 816 Coronands classification, 919 metal ion complexes, 928,938 Corphins, 855 Coninoids, 983 Corrins, 871-888 demetallation, 882 deuteration, 879 electrophilic reactions, 879 metallation, 882 NMR, 878 nucleophilicity, 886 nucleophilic reactions, 879 oxidation, 879 oxidative lactamization, 880 oxidative lactonization, 880 photochemistry, 887 reactions, 879 at metal, 885 rearrangements, 879 redox chemistry, 888 spectra, 877 synthesis, 878 Corroles, 871-888 demetallation, 874 deuteration, 872 hydrogenation, 872 metallation, 874 reactions, 872 at metal, 875 redox chemistry, 876 synthesis, 871 Corticotropin zinc complexes medical use, 966 Cotton effect anils, 717... 

Several chlorophyll derivatives have been prepared by electrophilic substitution, inter alia by formylation reactions. Adopting methods from corrin chemistry.50 alkylation with chloro-methyl methyl ether (caution toxic),32k chloromethyl methyl sulfide,51 and dichloromethyl methyl ether (caution toxic)52 in the presence of Lewis acids are the methods of choice to introduce carbon residues into the chlorin frame work. The compounds listed below have been prepared by these methods. 

The biomethylation reaction between platinum and methylcobalamin involves both platinum(II) and platinum(IV) oxidation states. An outer-sphere complex is formed between the charged platinum(II) salts and the corrin macrocycle, which catalytically labilizes the Co—C o bond to electrophilic attack. A two-electron redox switch mechanism has been proposed between platinum(II) and platinum(IV). However, a mechanism consistent with the kinetic data is direct electrophilic attack by PtClg on the Co—C a bond in MeBu. Studies on [Pt(NH3)2(OH2)2] indicate that the bases on cobalt interact in the coordination sphere of platinum(II). Since both platinum(ll) and platinum(rV) are together required to effect methyl transfer from methylcobalamin to platinuni, Pt and C NMR spectroscopy have been used to show that the methyl group is transferred to the platinum of the platinum(n) reactant. The kinetics of demethylation by mixtures of platinum(II) and platinum(IV) complexes show a lack of dependence on the axial ligand. The authors conclude therefore that it is unlikely that the reaction involves direct attack by the bound platinum on the Co—C bond, and instead favor electron transfer from an orbital on the corrin ring to the boimd platinum group in the slow step, followed by rapid methyl transfer. ... 

Imines are generally less electrophilic than the corresponding aldehyde but this diminished level of activity can be countered by suitable activation with Lewis acids. Formaldehyde imines are generally stable only at low temperatures and are best formed in situ. However, there are exceptions like Eschenmoser s salt 20. This methylene iminium salt is a relatively stable solid that is now commercially available. The utility of this reagent was illustrated in the Mannich reaction of corrin 19 with 20 to generated 21. 

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