Cobalt-catalyzed asymmetric hydrogenation of enamides enabled by single-electron reduction

Author:

Friedfeld Max R.1ORCID,Zhong Hongyu1ORCID,Ruck Rebecca T.2ORCID,Shevlin Michael2ORCID,Chirik Paul J.1ORCID

Affiliation:

1. Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.

2. Department of Process Research and Development, Merck Research Laboratories, Rahway, NJ 07065, USA.

Abstract

Reduction can make cobalt act precious Enzymes rely on abundant metals such as iron and nickel to manipulate hydrogen. Chemists, on the other hand, have largely had to rely on precious metals such as platinum and rhodium for the task. Friedfeld et al. now report a simple trick to make cobalt act more like rhodium. Reduction of Co(II) to Co(I) by zinc reinforced binding of phosphine ligands to the metal to facilitate its use in asymmetric hydrogenation of alkenes. The cobalt catalysts tolerated alcohol solvents, unlike their rhodium congeners, and could be applied to a 200-gram-scale reduction at 0.08% loading. Science , this issue p. 888

Funder

National Science Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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