Detalhe da pesquisa
1.
Deubiquitinase-targeting chimeras for targeted protein stabilization.
Nat Chem Biol
; 18(4): 412-421, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35210618
2.
Discovery of Potent Pyrazoline-Based Covalent SARS-CoV-2 Main Protease Inhibitors.
Chembiochem
; 24(11): e202300116, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37069799
3.
Enantioselective Rhodium(III)-Catalyzed Markovnikov Hydroboration of Unactivated Terminal Alkenes.
J Am Chem Soc
; 139(27): 9148-9151, 2017 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28665124
4.
Highly selective allylborations of aldehydes using α,α-disubstituted allylic pinacol boronic esters.
Angew Chem Int Ed Engl
; 53(24): 6145-9, 2014 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24799283
5.
Highly diastereo- and enantioselective allylboration of aldehydes using α-substituted allyl/crotyl pinacol boronic esters via in situ generated borinic esters.
J Am Chem Soc
; 135(14): 5316-9, 2013 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23520993
6.
Targeted Protein Degradation through E2 Recruitment.
ACS Chem Biol
; 18(4): 897-904, 2023 04 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36940189
7.
Correction to "Rational Chemical Design of Molecular Glue Degraders".
ACS Cent Sci
; 9(8): 1702, 2023 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37637749
8.
Rational Chemical Design of Molecular Glue Degraders.
ACS Cent Sci
; 9(5): 915-926, 2023 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37252349
9.
Diastereodivergent synthesis of trisubstituted alkenes through protodeboronation of allylic boronic esters: application to the synthesis of the Californian red scale beetle pheromone.
Angew Chem Int Ed Engl
; 51(50): 12444-8, 2012 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23129403
10.
A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core.
Chem Sci
; 11(43): 11897-11901, 2020 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34094417
11.
Application of the lithiation-borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes.
Chem Commun (Camb)
; 48(74): 9230-2, 2012 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-22609828