Twisted amides: from obscurity to broadly useful transition‐metal‐catalyzed reactions by N− C amide bond activation C Liu, M Szostak Chemistry–A European Journal 23 (30), 7157-7173, 2017 | 305 | 2017 |
Decarbonylative Phosphorylation of Amides by Palladium and Nickel Catalysis: The Hirao Cross‐Coupling of Amide Derivatives C Liu, M Szostak Angewandte Chemie International Edition 56 (41), 12718-12722, 2017 | 171 | 2017 |
Decarbonylative cross-coupling of amides C Liu, M Szostak Organic & Biomolecular Chemistry 16 (43), 7998-8010, 2018 | 154 | 2018 |
N-Acylsaccharins: Stable Electrophilic Amide-Based Acyl Transfer Reagents in Pd-Catalyzed Suzuki–Miyaura Coupling via N–C Cleavage C Liu, G Meng, Y Liu, R Liu, R Lalancette, R Szostak, M Szostak Organic letters 18 (17), 4194-4197, 2016 | 121 | 2016 |
Decarbonylative thioetherification by nickel catalysis using air-and moisture-stable nickel precatalysts C Liu, M Szostak Chemical communications 54 (17), 2130-2133, 2018 | 109 | 2018 |
Palladium‐Catalyzed Decarbonylative Borylation of Carboxylic Acids: Tuning Reaction Selectivity by Computation C Liu, CL Ji, X Hong, M Szostak Angewandte Chemie International Edition 57 (51), 16721-16726, 2018 | 105 | 2018 |
Acyl and Decarbonylative Suzuki Coupling of N-Acetyl Amides: Electronic Tuning of Twisted, Acyclic Amides in Catalytic Carbon–Nitrogen Bond Cleavage C Liu, G Li, S Shi, G Meng, R Lalancette, R Szostak, M Szostak ACS Catalysis 8 (10), 9131-9139, 2018 | 99 | 2018 |
N-Acylsaccharins as Amide-Based Arylating Reagents via Chemoselective N–C Cleavage: Pd-Catalyzed Decarbonylative Heck Reaction C Liu, G Meng, M Szostak The Journal of Organic Chemistry 81 (23), 12023-12030, 2016 | 91 | 2016 |
Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling of N-Mesylamides by N–C Cleavage: Electronic Effect of the Mesyl Group C Liu, Y Liu, R Liu, R Lalancette, R Szostak, M Szostak Organic letters 19 (6), 1434-1437, 2017 | 88 | 2017 |
Chemoselective Ketone Synthesis by the Addition of Organometallics to N-Acylazetidines C Liu, M Achtenhagen, M Szostak Organic letters 18 (10), 2375-2378, 2016 | 82 | 2016 |
Synthesis of Biaryls via Decarbonylative Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of Carboxylic Acids C Liu, CL Ji, ZX Qin, X Hong, M Szostak iscience 19, 749-759, 2019 | 70 | 2019 |
Bimetallic Cooperative Catalysis for Decarbonylative Heteroarylation of Carboxylic Acids via C‐O/C‐H Coupling C Liu, CL Ji, T Zhou, X Hong, M Szostak Angewandte Chemie International Edition 60 (19), 10690-10699, 2021 | 68 | 2021 |
n-BuLi as a Highly Efficient Precatalyst for Hydrophosphonylation of Aldehydes and Unactivated Ketones C Liu, Y Zhang, Q Qian, D Yuan, Y Yao Organic letters 16 (23), 6172-6175, 2014 | 58 | 2014 |
Highly-chemoselective step-down reduction of carboxylic acids to aromatic hydrocarbons via palladium catalysis C Liu, ZX Qin, CL Ji, X Hong, M Szostak Chemical Science 10 (22), 5736-5742, 2019 | 49 | 2019 |
N-Acylsuccinimides: Twist-controlled, acyl-transfer reagents in Suzuki–Miyaura cross-coupling by N–C amide bond activation Y Osumi, C Liu, M Szostak Organic & biomolecular chemistry 15 (42), 8867-8871, 2017 | 49 | 2017 |
Decarbonylative phosphorylation of carboxylic acids via redox-neutral palladium catalysis C Liu, CL Ji, T Zhou, X Hong, M Szostak Organic letters 21 (22), 9256-9261, 2019 | 46 | 2019 |
The most twisted acyclic amides: structures and reactivity C Liu, S Shi, Y Liu, R Liu, R Lalancette, R Szostak, M Szostak Organic letters 20 (24), 7771-7774, 2018 | 45 | 2018 |
Pd-catalyzed double-decarbonylative aryl sulfide synthesis through aryl exchange between amides and thioesters F Bie, X Liu, H Cao, Y Shi, T Zhou, M Szostak, C Liu Organic letters 23 (20), 8098-8103, 2021 | 32 | 2021 |
Sterically hindered ketones via palladium-catalyzed Suzuki–Miyaura cross-coupling of amides by N–C (O) activation C Liu, R Lalancette, R Szostak, M Szostak Organic letters 21 (19), 7976-7981, 2019 | 32 | 2019 |
Synthesis of Biaryls via Decarbonylative Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of Carboxylic Acids. iScience 2019, 19, 749–759 C Liu, CL Ji, ZX Qin, X Hong, M Szostak Eur. J. Org. Chem 1148, 2020 | 29 | 2020 |