Well-defined palladium (II)–NHC precatalysts for cross-coupling reactions of amides and esters by selective N–C/O–C cleavage S Shi, SP Nolan, M Szostak Accounts of Chemical Research 51 (10), 2589-2599, 2018 | 333 | 2018 |
Synthesis of Biaryls through Nickel‐Catalyzed Suzuki–Miyaura coupling of amides by carbon–nitrogen bond cleavage S Shi, G Meng, M Szostak Angewandte Chemie 128 (24), 7073-7077, 2016 | 312 | 2016 |
Cross-coupling of amides by N–C bond activation G Meng, S Shi, M Szostak Synlett 27 (18), 2530-2540, 2016 | 233 | 2016 |
Metal-free transamidation of secondary amides via selective N–C cleavage under mild conditions Y Liu, S Shi, M Achtenhagen, R Liu, M Szostak Organic letters 19 (7), 1614-1617, 2017 | 174 | 2017 |
Pd–PEPPSI: a general Pd–NHC precatalyst for Buchwald–Hartwig cross-coupling of esters and amides (transamidation) under the same reaction conditions S Shi, M Szostak Chemical communications 53 (76), 10584-10587, 2017 | 163 | 2017 |
Suzuki–Miyaura cross-coupling of amides and esters at room temperature: correlation with barriers to rotation around C–N and C–O bonds P Lei, G Meng, S Shi, Y Ling, J An, R Szostak, M Szostak Chemical science 8 (9), 6525-6530, 2017 | 163 | 2017 |
Reversible Twisting of Primary Amides via Ground State N–C (O) Destabilization: Highly Twisted Rotationally Inverted Acyclic Amides G Meng, S Shi, R Lalancette, R Szostak, M Szostak Journal of the American Chemical Society 140 (2), 727-734, 2018 | 159 | 2018 |
Palladium-catalyzed Suzuki–Miyaura cross-coupling of amides via site-selective N–C bond cleavage by cooperative catalysis G Meng, S Shi, M Szostak Acs Catalysis 6 (11), 7335-7339, 2016 | 147 | 2016 |
Ground-State Distortion in N-Acyl-tert-butyl-carbamates (Boc) and N-Acyl-tosylamides (Ts): Twisted Amides of Relevance to Amide N–C Cross-Coupling R Szostak, S Shi, G Meng, R Lalancette, M Szostak The Journal of organic chemistry 81 (17), 8091-8094, 2016 | 134 | 2016 |
Efficient Synthesis of Diaryl Ketones by Nickel‐Catalyzed Negishi Cross‐Coupling of Amides by Carbon–Nitrogen Bond Cleavage at Room Temperature Accelerated by a Solvent Effect S Shi, M Szostak Chemistry–A European Journal 22 (30), 10420-10424, 2016 | 127 | 2016 |
Nickel-Catalyzed Diaryl Ketone Synthesis by N–C Cleavage: Direct Negishi Cross-Coupling of Primary Amides by Site-Selective N,N-Di-Boc Activation S Shi, M Szostak Organic letters 18 (22), 5872-5875, 2016 | 119 | 2016 |
Structures of Highly Twisted Amides Relevant to Amide N− C Cross‐Coupling: Evidence for Ground‐State Amide Destabilization V Pace, W Holzer, G Meng, S Shi, R Lalancette, R Szostak, M Szostak Chemistry–A European Journal 22 (41), 14494-14498, 2016 | 109 | 2016 |
Decarbonylative cyanation of amides by palladium catalysis S Shi, M Szostak Organic letters 19 (12), 3095-3098, 2017 | 108 | 2017 |
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 | 96 | 2018 |
Pd-PEPPSI: A General Pd-NHC Precatalyst for Suzuki–Miyaura Cross-Coupling of Esters by C–O Cleavage S Shi, P Lei, M Szostak Organometallics 36 (19), 3784-3789, 2017 | 72 | 2017 |
Aminoketyl Radicals in Organic Synthesis: Stereoselective Cyclization of Five- and Six-Membered Cyclic Imides to 2-Azabicycles Using SmI2–H2O S Shi, M Szostak organic letters 17 (20), 5144–5147, 2015 | 64 | 2015 |
Pd‐PEPPSI: Water‐Assisted Suzuki− Miyaura Cross‐Coupling of Aryl Esters at Room Temperature using a Practical Palladium‐NHC (NHC= N‐Heterocyclic Carbene) Precatalyst G Li, S Shi, P Lei, M Szostak Advanced Synthesis & Catalysis 360 (7), 1538-1543, 2018 | 54 | 2018 |
Nickel-catalyzed Negishi cross-coupling of N-acylsuccinimides: stable, amide-based, twist-controlled acyl-transfer reagents via N–C activation S Shi, M Szostak Synthesis 49 (16), 3602-3608, 2017 | 49 | 2017 |
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 | 44 | 2018 |
Triflamides: Highly Reactive, Electronically Activated N-Sulfonyl Amides in Catalytic N–C(O) Amide Cross-Coupling S Shi, R Lalancette, R Szostak, M Szostak Organic letters 21 (5), 1253-1257, 2019 | 38 | 2019 |