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Journal of the American Chemical Society|January 8, 2015
Virtually instantaneous, room-temperature [(11)C]-cyanation using biaryl phosphine Pd(0) complexesHong Geun Lee, Phillip J Milner, Michael S Placzek, et al.
Journal of the American Chemical Society|March 1, 2019
CuH-Catalyzed Enantioselective Ketone Allylation with 1,3-Dienes: Scope, Mechanism, and ApplicationsChengxi Li, Richard Y Liu, Luke T Jesikiewicz, et al.
Journal of the American Chemical Society|August 4, 2023
Stereoselective Synthesis of Trisubstituted Alkenes via Copper Hydride-Catalyzed Alkyne HydroalkylationDennis A Kutateladze, Binh Khanh Mai, Yuyang Dong, et al.
Organic Letters|November 2, 2021
A Dual CuH- and Pd-Catalyzed Stereoselective Synthesis of Highly Substituted 1,3-DienesChuan-Jin Hou, Alexander W Schuppe, James Levi Knippel, et al.
Science (New York, N.Y.)|June 26, 2010
The palladium-catalyzed trifluoromethylation of aryl chloridesEun Jin Cho, Todd D Senecal, Tom Kinzel, et al.
Journal of the American Chemical Society|October 18, 2011
Evidence for in situ catalyst modification during the Pd-catalyzed conversion of aryl triflates to aryl fluoridesThomas J Maimone, Phillip J Milner, Tom Kinzel, et al.
The Journal of Organic Chemistry|August 30, 2008
Palladium-catalyzed carbonylation reactions of aryl bromides at atmospheric pressure: a general system based on XantphosJoseph R Martinelli, Donald A Watson, Dominique M M Freckmann, et al.
Journal of the American Chemical Society|May 5, 2020
Protein-Protein Cross-Coupling via Palladium-Protein Oxidative Addition Complexes from Cysteine ResiduesHeemal H Dhanjee, Azin Saebi, Ivan Buslov, et al.
Journal of the American Chemical Society|January 12, 2026
Catellani-Inspired BN-Aromatic Expansion: A Versatile Tool toward π-Extended 1,2-Azaborines with Tunable Photosensitizing PropertiesFederica Rulli, Sergi Ordeix, Roger Bresolí-Obach, et al.
Science (New York, N.Y.)|August 15, 2009
Formation of ArF from LPdAr(F): catalytic conversion of aryl triflates to aryl fluoridesDonald A Watson, Mingjuan Su, Georgiy Teverovskiy, et al.
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