E-mail a Wiley Online Library Link

Prof. Dr. Wolfgang Buckel, Dr. Peter Friedrich and Prof. Dr. Bernard T. Golding Hydrogen Bonds Guide the Short-Lived 5′-Deoxyadenosyl Radical to the Place of Action Angewandte Chemie International Edition 51

Version of Record online: 3 SEP 2012 | DOI: 10.1002/anie.201205299

Thumbnail image of graphical abstract

Radical chaperone: Recent research reveals how the 5′-deoxyadenosyl radical (see structure) is generated by homolysis of the Co[BOND]C σ-bond of enzyme-bound coenzyme B12 and how it is guided to the substrate through pseudorotation of the ribose moiety and hydrogen-bonding interactions.

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field