Detalhe da pesquisa
1.
Quinone-mediated hydrogen anode for non-aqueous reductive electrosynthesis.
Nature
; 623(7985): 71-76, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37604186
2.
The hydrogen-bonding dynamics of water to a nitrile-functionalized electrode is modulated by voltage according to ultrafast 2D IR spectroscopy.
Proc Natl Acad Sci U S A
; 120(52): e2314998120, 2023 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38127983
3.
Cavity Quantum Electrodynamics Enables para- and ortho-Selective Electrophilic Bromination of Nitrobenzene.
J Am Chem Soc
; 146(23): 16184-16193, 2024 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38814893
4.
Computationally Guided Ligand Discovery from Compound Libraries and Discovery of a New Class of Ligands for Ni-Catalyzed Cross-Electrophile Coupling of Challenging Quinoline Halides.
J Am Chem Soc
; 146(10): 6947-6954, 2024 Mar 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38427582
5.
Computational Methods Enable the Prediction of Improved Catalysts for Nickel-Catalyzed Cross-Electrophile Coupling.
J Am Chem Soc
; 146(5): 3043-3051, 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38276910
6.
Reductive Arylation of Nitroarenes with Chloroarenes: Reducing Conditions Enable New Reactivity from Palladium Catalysts.
J Am Chem Soc
; 145(29): 16150-16159, 2023 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37437188
7.
Multimetallic-Catalyzed C-C Bond-Forming Reactions: From Serendipity to Strategy.
J Am Chem Soc
; 145(12): 6596-6614, 2023 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36913663
8.
Formation of C(sp2)-C(sp3) Bonds Instead of Amide C-N Bonds from Carboxylic Acid and Amine Substrate Pools by Decarbonylative Cross-Electrophile Coupling.
J Am Chem Soc
; 145(18): 9951-9958, 2023 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37126234
9.
Protodemetalation of (Bipyridyl)Ni(II)-Aryl Complexes Shows Evidence for Five-, Six-, and Seven-Membered Cyclic Pathways.
J Am Chem Soc
; 2023 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37026854
10.
CdS Quantum Dots as Potent Photoreductants for Organic Chemistry Enabled by Auger Processes.
J Am Chem Soc
; 144(27): 12229-12246, 2022 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35772053
11.
Control of Redox-Active Ester Reactivity Enables a General Cross-Electrophile Approach to Access Arylated Strained Rings.
Angew Chem Int Ed Engl
; 61(33): e202205673, 2022 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35688769
12.
A General, Multimetallic Cross-Ullmann Biheteroaryl Synthesis from Heteroaryl Halides and Heteroaryl Triflates.
J Am Chem Soc
; 143(51): 21484-21491, 2021 12 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34918908
13.
ChemBead Enabled High-Throughput Cross-Electrophile Coupling Reveals a New Complementary Ligand.
Chemistry
; 27(51): 12981-12986, 2021 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34233043
14.
Multimetallic catalysed cross-coupling of aryl bromides with aryl triflates.
Nature
; 524(7566): 454-7, 2015 Aug 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-26280337
15.
Sulfonate Versus Sulfonate: Nickel and Palladium Multimetallic Cross-Electrophile Coupling of Aryl Triflates with Aryl Tosylates.
J Am Chem Soc
; 142(24): 10634-10640, 2020 06 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32486635
16.
Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Chlorides with Primary Alkyl Chlorides.
J Am Chem Soc
; 142(22): 9902-9907, 2020 06 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32412241
17.
Nickel-Catalyzed Synthesis of Dialkyl Ketones from the Coupling of N-Alkyl Pyridinium Salts with Activated Carboxylic Acids.
Angew Chem Int Ed Engl
; 59(32): 13484-13489, 2020 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32374951
18.
Nickel-Catalyzed Addition of Aryl Bromides to Aldehydes To Form Hindered Secondary Alcohols.
J Am Chem Soc
; 141(5): 1823-1827, 2019 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30693771
19.
LiCl-Accelerated Multimetallic Cross-Coupling of Aryl Chlorides with Aryl Triflates.
J Am Chem Soc
; 141(28): 10978-10983, 2019 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31257881
20.
Ruthenium-Catalyzed C-H Arylation of 1-Naphthol with Aryl and Heteroaryl Halides.
J Org Chem
; 84(23): 15642-15647, 2019 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31725290