Matthew T. Richers

Redox-Neutral α-Oxygenation of Amines: Reaction Development and Elucidation of the Mechanism

Matthew T. Richers, Martin Breugst, A. Yu. Platonova et al. · Journal of the American Chemical Society · 2014 · 146 citations · Full text

Metal-Free α-Amination of Secondary Amines: Computational and Experimental Evidence for Azaquinone Methide and Azomethine Ylide Intermediates

Arne Dieckmann, Matthew T. Richers, A. Yu. Platonova et al. · The Journal of Organic Chemistry · 2013 · 82 citations

Combinatorial Chemistry, Engineering, Reactive Intermediates +10

The Decarboxylative Strecker Reaction

Deepankar Das, Matthew T. Richers, Longle Ma et al. · Organic Letters · 2011 · 71 citations

Redox-Neutral α-Sulfenylation of Secondary Amines: Ring-Fused <i>N</i>,<i>S</i>-Acetals

Claire L. Jarvis, Matthew T. Richers, Martin Breugst et al. · Organic Letters · 2014 · 64 citations · Full text

Engineering, Computational Studies, Organic Chemistry +8

Facile Access to Ring-Fused Aminals via Direct α-Amination of Secondary Amines with o-Aminobenzaldehydes: Synthesis of Vasicine, Deoxyvasicine, Deoxyvasicinone, Mackinazolinone, and Ruteacarpine

Daniel Seidel, Matthew T. Richers, Indubhusan Deb et al. · Synthesis · 2013 · 51 citations

Combinatorial Chemistry, Medicinal Chemistry, Ring-fused Aminals +15