Detalhe da pesquisa
1.
Metal-free photoinduced C(sp3)-H borylation of alkanes.
Nature
; 586(7831): 714-719, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33116286
2.
Simultaneous Stereoinvertive and Stereoselective C(sp3)-C(sp3) Cross-Coupling of Boronic Esters and Allylic Carbonates.
J Am Chem Soc
; 146(20): 13719-13726, 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38721780
3.
Convergent Deboronative and Decarboxylative Phosphonylation Enabled by the Phosphite Radical Trap "BecaP".
J Am Chem Soc
; 145(33): 18649-18657, 2023 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37552886
4.
Copper-Mediated Dehydrogenative C(sp3)-H Borylation of Alkanes.
J Am Chem Soc
; 145(28): 15207-15217, 2023 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37410056
5.
Iridium-Catalyzed Asymmetric Difunctionalization of C-C σ-Bonds Enabled by Ring-Strained Boronate Complexes.
J Am Chem Soc
; 145(30): 16508-16516, 2023 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37471704
6.
De Novo Synthesis of Dihydrobenzofurans and Indolines and Its Application to a Modular, Asymmetric Synthesis of Beraprost.
J Am Chem Soc
; 145(25): 14124-14132, 2023 Jun 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37326516
7.
Synthesis and Applications of Bicyclo[1.1.0]butyl and Azabicyclo[1.1.0]butyl Organometallics.
Chemistry
; 29(29): e202300008, 2023 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36786481
8.
Synergy of synthesis, computation and NMR reveals correct baulamycin structures.
Nature
; 547(7664): 436-440, 2017 07 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28748934
9.
Strain-Release Driven Epoxidation and Aziridination of Bicyclo[1.1.0]butanes via Palladium Catalyzed σ-Bond Nucleopalladation.
Angew Chem Int Ed Engl
; 62(7): e202217064, 2023 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36507714
10.
Photoredox-Catalyzed Decarboxylative Bromination, Chlorination and Thiocyanation Using Inorganic Salts.
Angew Chem Int Ed Engl
; 62(38): e202309684, 2023 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37522816
11.
Conformationally Controlled sp3 -Hydrocarbon-Based α-Helix Mimetics.
Angew Chem Int Ed Engl
; 62(23): e202301209, 2023 06 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37017133
12.
Stereospecific Conversion of Boronic Esters into Enones using Methoxyallene: Application in the Total Synthesis of 10-Deoxymethynolide.
Angew Chem Int Ed Engl
; 62(50): e202312054, 2023 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37877778
13.
Stereocontrolled Total Synthesis of Bastimolide B Using Iterative Homologation of Boronic Esters.
J Am Chem Soc
; 144(18): 7995-8001, 2022 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35499478
14.
Four-Component Strain-Release-Driven Synthesis of Functionalized Azetidines.
Angew Chem Int Ed Engl
; 61(52): e202214049, 2022 12 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36300572
15.
Strain-Release-Driven Friedel-Crafts Spirocyclization of Azabicyclo[1.1.0]butanes.
Angew Chem Int Ed Engl
; 61(3): e202114235, 2022 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34780681
16.
Diastereodivergent Synthesis of Cyclopentyl Boronic Esters Bearing Contiguous Fully Substituted Stereocenters.
Angew Chem Int Ed Engl
; 61(35): e202205816, 2022 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35639345
17.
Facile Conversion of α-Amino Acids into α-Amino Phosphonates by Decarboxylative Phosphorylation using Visible-Light Photocatalysis.
Angew Chem Int Ed Engl
; 61(37): e202207063, 2022 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35851520
18.
Selective Coupling of 1,2-Bis-Boronic Esters at the more Substituted Site through Visible-Light Activation of Electron Donor-Acceptor Complexes.
Angew Chem Int Ed Engl
; 61(18): e202202061, 2022 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35213775
19.
Dual Nickel/Photoredox-Catalyzed Site-Selective Cross-Coupling of 1,2-Bis-Boronic Esters Enabled by 1,2-Boron Shifts.
Angew Chem Int Ed Engl
; 61(34): e202207988, 2022 08 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35779000
20.
Dual-Gradient Unified Chromatography: A New Paradigm for Versatility in Simultaneous Multicomponent Analysis.
Angew Chem Int Ed Engl
; 61(45): e202208854, 2022 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36111975