Shicheng Shi

发表

Synthesis of Biaryls through Nickel-Catalyzed Suzuki-Miyaura Coupling of Amides by Carbon-Nitrogen Bond Cleavage.

M. Szostak, Shicheng Shi, Guangrong Meng, 2016, Angewandte Chemie.

Proton-coupled electron transfer in the reduction of carbonyls using SmI2-H2O: implications for the reductive coupling of acyl-type ketyl radicals with SmI2-H2O.

R. Szostak, M. Szostak, Shicheng Shi, 2016, Organic & biomolecular chemistry.

Suzuki–Miyaura cross-coupling of amides and esters at room temperature: correlation with barriers to rotation around C–N and C–O bonds

R. Szostak, M. Szostak, Shicheng Shi, 2017, Chemical science.

Aminoketyl Radicals in Organic Synthesis: Stereoselective Cyclization of Five- and Six-Membered Cyclic Imides to 2-Azabicycles Using SmI2-H2O.

M. Szostak, Shicheng Shi, 2015, Organic letters.

The Most Twisted Acyclic Amides: Structures and Reactivity.

R. Szostak, R. Lalancette, M. Szostak, 2018, Organic letters.

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, R. Lalancette, M. Szostak, 2016, The Journal of organic chemistry.

Synthesis of 4‐(2‐Phenylhydrazono)‐1‐(4‐phenylthiazol‐2‐yl)‐1H‐pyrazol‐5(4H)‐one Compounds and Characterization of Their Affinities to Anti‐apoptotic Bcl‐2 Family Proteins

Renxiao Wang, Biao Yu, Zhen Liu, 2013 .

Nickel-Catalyzed Diaryl Ketone Synthesis by N-C Cleavage: Direct Negishi Cross-Coupling of Primary Amides by Site-Selective N,N-Di-Boc Activation.

M. Szostak, Shicheng Shi, 2016, Organic letters.

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.

M. Szostak, Shicheng Shi, 2016, Chemistry.

Mechanistic Study of SmI2/H2O and SmI2/Amine/H2O-Promoted Chemoselective Reduction of Aromatic Amides (Primary, Secondary, Tertiary) to Alcohols via Aminoketyl Radicals.

M. Szostak, Shicheng Shi, S. R. Huq, 2017, The Journal of organic chemistry.

Metal-Free Transamidation of Secondary Amides via Selective N-C Cleavage under Mild Conditions.

M. Szostak, Shicheng Shi, Ruzhang Liu, 2017, Organic letters.

Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling of Amides via Site-Selective N–C Bond Cleavage by Cooperative Catalysis

M. Szostak, Shicheng Shi, Guangrong Meng, 2016 .

[(NHC)PdCl2(Aniline)] Complexes: Easily Synthesized, Highly Active Pd(II)-NHC Precatalysts for Cross-Coupling Reactions.

R. Szostak, R. Lalancette, M. Szostak, 2021, The Journal of organic chemistry.

Well-Defined Palladium(II)-NHC Precatalysts for Cross-Coupling Reactions of Amides and Esters by Selective N-C/O-C Cleavage.

S. Nolan, M. Szostak, Shicheng Shi, 2018, Accounts of chemical research.

Cross-Coupling of Amides by N–C Bond Activation

M. Szostak, Shicheng Shi, Guangrong Meng, 2016, Synlett.

Decarbonylative Borylation of Amides by Palladium Catalysis

M. Szostak, Shicheng Shi, 2019, ACS omega.

Pd-PEPPSI: Water-Assisted Suzuki−Miyaura Cross-Coupling of Aryl Esters at Room Temperature using a Practical Palladium-NHC (NHC=N-Heterocyclic Carbene) Precatalyst

M. Szostak, Shicheng Shi, Guangchen Li, 2018 .

Pd-PEPPSI: A General Pd-NHC Precatalyst for Suzuki–Miyaura Cross-Coupling of Esters by C–O Cleavage

M. Szostak, Shicheng Shi, P. Lei, 2017 .

Pd-PEPPSI: a general Pd-NHC precatalyst for Buchwald-Hartwig cross-coupling of esters and amides (transamidation) under the same reaction conditions.

M. Szostak, Shicheng Shi, 2017, Chemical communications.

Decarbonylative Cyanation of Amides by Palladium Catalysis.

M. Szostak, Shicheng Shi, 2017, Organic letters.

Structures of Highly Twisted Amides Relevant to Amide N-C Cross-Coupling: Evidence for Ground-State Amide Destabilization.

R. Szostak, R. Lalancette, Vittorio Pace, 2016, Chemistry.

Acyl and Decarbonylative Suzuki Coupling of N-Acetyl Amides: Electronic Tuning of Twisted, Acyclic Amides in Catalytic Carbon–Nitrogen Bond Cleavage

R. Szostak, R. Lalancette, M. Szostak, 2018, ACS Catalysis.

Triflamides: Highly Reactive, Electronically Activated N-Sulfonyl Amides in Catalytic N-C(O) Amide Cross-Coupling.

R. Szostak, R. Lalancette, M. Szostak, 2019, Organic letters.

Reversible Twisting of Primary Amides via Ground State N-C(O) Destabilization: Highly Twisted Rotationally Inverted Acyclic Amides.

R. Szostak, R. Lalancette, M. Szostak, 2018, Journal of the American Chemical Society.

Nickel-Catalyzed Negishi Cross-Coupling of N-Acylsuccinimides: Stable, Amide-Based, Twist-Controlled Acyl-Transfer Reagents via N–C Activation

M. Szostak, Shicheng Shi, 2017 .

Synthesis of Nitrogen Heterocycles Using Samarium(II) Iodide

M. Szostak, Shicheng Shi, 2017, Molecules.

Catalytic Cycloisomerization onto a Carbonyl Oxygen.

J. Norton, Tao Chen, Shicheng Shi, 2020, Organic letters.

Synthesis of Biaryls Through Nickel‐Catalyzed Suzuki—Miyaura Coupling of Amides by Carbon—Nitrogen Bond Cleavage.

M. Szostak, Shicheng Shi, Guangrong Meng, 2016 .

N-Halo succinimide-promoted one-pot three-component electrophilic cyclization: Facile access to dihalogenated heterocycles under mild conditions

Mingjin Fan, Desuo Yang, Shicheng Shi, 2017 .

Highly Chemoselective Synthesis of Indolizidine Lactams by SmI2 -Induced Umpolung of the Amide Bond via Aminoketyl Radicals: Efficient Entry to Alkaloid Scaffolds.

R. Szostak, R. Lalancette, M. Szostak, 2016, Chemistry.

17O NMR and 15N NMR chemical shifts of sterically-hindered amides: ground-state destabilization in amide electrophilicity.

R. Szostak, Laura Ielo, Vittorio Pace, 2019, Chemical communications.

Reversible Twisting of Primary Amides via Ground State N-C(O) Destabilization: Highly Twisted Rotationally Inverted Acyclic Amides.

R. Szostak, R. Lalancette, M. Szostak, 2018, Journal of the American Chemical Society.

Proton-coupled electron transfer in the reduction of carbonyls using SmI2-H2O: implications for the reductive coupling of acyl-type ketyl radicals with SmI2-H2O.

R. Szostak, M. Szostak, Shicheng Shi, 2016, Organic & biomolecular chemistry.