Pyridylidene‐Mediated Dihydrogen Activation Coupled with Catalytic Imine Reduction1. Issue 33 (26th June 2015)

• Record Type: Journal Article
• Authors: Auth, Johanna; Padevet, Jaroslav; Mauleón, Pablo; Pfaltz, Andreas
• Is Part Of: Angewandte Chemie international edition. Volume 54:Issue 33(2015)
• Page Start: 9542
• Page End: 9545
• Publication Date: 2015-06-26
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201503233
• Languages: English
• ISSNs: 1433-7851

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In recent years, dihydrogen activation at non‐metallic centers has received increasing attention. A system in which dihydrogen is trapped by a pyridylidene intermediate that is generated from a pyridinium salt and a base is now reported. The dihydropyridine formed in this process can act as reducing agent towards organic electrophiles. By coupling the hydrogen‐activation step with subsequent hydride transfer from the dihydropyridine to an imine, a catalytic process was established. Treatment of the <italic>N</italic>‐phenylimine of phenyl trifluoromethyl ketone with 5–20 mol % of <italic>N‐</italic>mesityl‐3, 5‐bis(2, 6‐dimethylphenyl)pyridinium triflate and 0.3–1.0 equivalents of LiN(SiMe₃)₂ under 50 bar of hydrogen gas resulted in high conversion into the corresponding amine.</p> </abstract>