Sophia’s study on how metal catalysts can allow hydrogen gas to drive part of the reverse Krebs cycle under mild nonenzymatic conditions has been accepted for publication in Angewandte Chemie International Edition. She even found that iron-based meteorites can promote these reactions! Congrats!
Robert’s mechanistic study on reduction and reductive amination of ketoacids under simple nonenzymatic conditions has been accepted for publication in Angewandte Chemie International Edition. Congrats and impressive work!
Marie’s paper on the generation of trifluoromethylated all-carbon quaternary centres through the hydroarylation of trifluoromethylated styrenes is accepted for publication in ACS Catalysis. Thanks to Robert for the last-minute mechanistic help. Congrats!
Joseph reviews Nick Lane’s new book on the Krebs cycle for Science. Please have a read (the review and the book itself)!
Nik, Sergiu and Robert’s paper on how HFIP facilitates enamide hydroarylation is accepted for publication in Chemical Science. Lots of important mechanistic insight in this one and a great example of how collaboration makes a paper better. Congrats!
Jing’s work on a non enzymatic analog of pyrimidine nucleobase biosynthesis has been accepted for publication in Angewandte Chemie International Edition. Congrats!
Marie and Shaofei’s rapid method for the reduction of epoxides to primary alcohols has been accepted for publication in ACS Catalysis. Congrats!
Our paper on a large expansion of the Friedel-Crafts reaction has been accepted for publication in Chem. We describe Friedel-Crafts reactions with primary aliphatic alcohols and electronically deactivated epoxides, as well as sequential Friedel-Crafts reactions stemming from epoxide-opening, all without pre-activation. This was a massive project with over 170 examples, some of it reaching back nearly 4 years. Congrats to Shaofei, Marie, Florent, Vuk and Andrei and to our DFT collaborators in the Rowley lab (Carleton).
Robert, Harpreet and Sophia’s re-evaluation and mechanistic study of metal ion-catalyzed transamination under biological conditions has been accepted for publication in the Journal of the American Chemical Society. Congrats!
Our article on expanding the Suzuki-Miyaura coupling to aryl sulfonyl fluorides has been accepted for publication in Angewandte Chemie International Edition. Special thanks to Maryam Bahadori and Chris Rowley (Carleton University) for the DFT calculations. Congrats to Paul and the rest of the team!
Abhijit thanks the EU for a H2020 Marie Skłodowska Curie Fellowship (project 792101)!
The Moran Research Group 