Sustainable radical reduction through catalytic hydrogen atom transfer.

A system with coupled catalytic cycles is described that allows radical reduction by hydrogen atom abstraction from rhodium hydrides. These intermediates are generated from H2 activation by Wilkinson's catalyst. Radical generation is carried out by titanocene-catalyzed electron transfer to epoxides.

Titanocene catalyzed 4-exo cyclizations: mechanism, experiment, catalyst design.

A method for the preparation of a variety of cyclobutanes via 4-exo cyclization of radicals is presented. Radical generation is carried out by electron transfer from titanocene(III) chlorides to epoxides. The reaction relies on the acceleration of the cyclization through the use of alpha,beta-unsaturated carbonyl compounds as radical traps and the thermodynamic stabilization of the cyclobutylcarbinyl radicals through conjugation.

Easy one-pot synthesis of new dppm-type linkers for immobilizations.

New synthetic routes to symmetric and unsymmetric dppm-type chelate linkers containing the ethoxysilane group are described and the compounds were characterized also by solid-state NMR spectroscopy and X-ray structures.