ADVANCES IN ENZYMOLOGY

@inproceedings{Enzymology2013ADVANCESIE,
  title={ADVANCES IN ENZYMOLOGY},
  author={Advances IN Enzymology},
  year={2013}
}
ion of the bromine atom from the benzaldimine of 2-methyl-3-bromoalanine ethyl ester produces the 3-radical, which is either quenched or undergoes rearrangement to the 2-radical. Quenching of the 2-radical produces the rearrangement product (29). This reaction is thought to be a model for the action of PLP in facilitating a,p-imino rearrangements of radical intermediates in aminomutase reactions. 16 PERRY A. FREY AND GEORGE H. REED Figure 3. A hypothetical mechanism for the a,p-imino… Expand

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