Detalhe da pesquisa
1.
Deacylative transformations of ketones via aromatization-promoted C-C bond activation.
Nature
; 567(7748): 373-378, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30758326
2.
Mechanistic Investigation into Single-Electron Oxidative Addition of Single-Atom Cu(I)-N4 Site: Revealing the Cu(I)-Cu(II)-Cu(I) Catalytic Cycle in Photochemical Hydrophosphinylation.
J Am Chem Soc
; 146(12): 8668-8676, 2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38498937
3.
Prediction of flood sensitivity based on Logistic Regression, eXtreme Gradient Boosting, and Random Forest modeling methods.
Water Sci Technol
; 89(10): 2605-2624, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38822603
4.
Diborodichloromethane as Versatile Reagent for Chemodivergent Synthesis of gem-Diborylalkanes.
Angew Chem Int Ed Engl
; 63(3): e202315227, 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38059834
5.
Unraveling the Structure and Reactivity Patterns of the Indole Radical Cation in Regioselective Electrochemical Oxidative Annulations.
J Am Chem Soc
; 145(5): 3175-3186, 2023 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36705997
6.
Triflylpyridinium Enables Rapid and Scalable Controlled Reduction of Carboxylic Acids to Aldehydes using Pinacolborane.
Angew Chem Int Ed Engl
; 62(2): e202215168, 2023 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36378536
7.
Electrooxidative Activation of B-B Bond in B2 cat2 : Access to gem-Diborylalkanes via Paired Electrolysis.
Angew Chem Int Ed Engl
; 62(14): e202218179, 2023 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-36722684
8.
Palladium/Norbornene-Catalyzed Direct Vicinal Di-Carbo-Functionalization of Indoles: Reaction Development and Mechanistic Study.
Angew Chem Int Ed Engl
; 62(43): e202310697, 2023 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37672173
9.
Electroreduction Enables Regioselective 1,2-Diarylation of Alkenes with Two Electrophiles.
Angew Chem Int Ed Engl
; 62(17): e202219166, 2023 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36826413
10.
Epoxide Electroreduction.
J Am Chem Soc
; 144(3): 1389-1395, 2022 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-34963293
11.
Iridium-Catalyzed Intramolecular ß-C-H Alkenylation of Ketones with Alkynes via a Hydride-Transfer Approach.
J Am Chem Soc
; 144(50): 23230-23238, 2022 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36508583
12.
Switchable Radical Carbonylation by Philicity Regulation.
J Am Chem Soc
; 144(32): 14923-14935, 2022 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35939790
13.
Remote Enantioselective [4 + 1] Annulation with Copper-Vinylvinylidene Intermediates.
J Am Chem Soc
; 144(46): 21347-21355, 2022 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36367320
14.
Catalytic Asymmetric Vinylogous and Bisvinylogous Propargylic Substitution.
J Am Chem Soc
; 144(34): 15779-15785, 2022 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-35976107
15.
Chemical Recycling of Polystyrene to Valuable Chemicals via Selective Acid-Catalyzed Aerobic Oxidation under Visible Light.
J Am Chem Soc
; 144(14): 6532-6542, 2022 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35353526
16.
Recent Advances in Theoretical Studies on Transition-Metal-Catalyzed Carbene Transformations.
Acc Chem Res
; 54(14): 2905-2915, 2021 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34232609
17.
ProPhenol Derived Ligands to Simultaneously Coordinate a Main-Group Metal and a Transition Metal: Application to a Zn-Cu Catalyzed Reaction.
Chemistry
; 28(9): e202104268, 2022 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34902190
18.
Diastereoselective Transfer of Tri(di)fluoroacetylsilanes-Derived Carbenes to Alkenes.
Angew Chem Int Ed Engl
; 61(25): e202202175, 2022 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35415937
19.
From Esters to Ketones via a Photoredox-Assisted Reductive Acyl Cross-Coupling Strategy.
Angew Chem Int Ed Engl
; 61(3): e202114731, 2022 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34783143
20.
Photoinduced Copper-Catalyzed Asymmetric C(sp3 )-H Alkynylation of Cyclic Amines by Intramolecular 1,5-Hydrogen Atom Transfer.
Angew Chem Int Ed Engl
; 61(34): e202208232, 2022 Aug 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35751507