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Nature Communications|October 25, 2017
A three-membered ring approach to carbonyl olefinationSupaporn Niyomchon, Alberto Oppedisano, Paul Aillard, et al.Angewandte Chemie (International Ed. in English)|April 18, 2014
Chemoselective intermolecular α-arylation of amidesBo Peng, Danny Geerdink, Christophe Farès, et al.Angewandte Chemie (International Ed. in English)|June 4, 2014
Asymmetric palladium-catalyzed allylic alkylation using dialkylzinc reagents: a remarkable ligand effectAntonio Misale, Supaporn Niyomchon, Marco Luparia, et al.Journal of the American Chemical Society|December 23, 2008
Ruthenium-catalyzed cross-coupling of tertiary propargyl alcohols with omega-alkynenitriles: a regio- and stereoselective surrogate for an aldol condensationBarry M Trost, Nuno Maulide, Michael T RuddChemical Communications (Cambridge, England)|August 5, 2015
A family of low molecular-weight, organic catalysts for reductive C-C bond formationSaad Shaaban, Anaïs Jolit, Desislava Petkova, et al.Journal of the American Chemical Society|May 10, 2017
Flexible and Chemoselective Oxidation of Amides to α-Keto Amides and α-Hydroxy AmidesAurélien de la Torre, Daniel Kaiser, Nuno MaulideChemical Society Reviews|August 29, 2018
Amide activation: an emerging tool for chemoselective synthesisDaniel Kaiser, Adriano Bauer, Miran Lemmerer, et al.Angewandte Chemie (International Ed. in English)|July 11, 2017
Hydroxamic Acids as Chemoselective (ortho-Amino)arylation Reagents via Sigmatropic RearrangementSaad Shaaban, Veronica Tona, Bo Peng, et al.Angewandte Chemie (International Ed. in English)|October 23, 2025
Facile (Z)-Selective Synthesis of β,γ-Unsaturated Ketones by a Silicon-based Olefination StrategyDaniya Aynetdinova, Jakub Brześkiewicz, Nikolaos Skoulikas, et al.Nature Chemistry|October 20, 2022
Inverse hydride shuttle catalysis enables the stereoselective one-step synthesis of complex frameworksImmo Klose, Giovanni Di Mauro, Dainis Kaldre, et al.Pageof 19