Detalhe da pesquisa
1.
Dual-Catalytic Enantioselective Allylation of N-(Heteroaromatic-methyl)imine Derivatives.
J Org Chem
; 88(12): 7821-7829, 2023 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36562778
2.
Homologation of Electron-Rich Benzyl Bromide Derivatives via Diazo C-C Bond Insertion.
J Am Chem Soc
; 144(1): 86-92, 2022 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34898193
3.
Reagent Control Enables Selective and Regiodivergent Opening of Unsymmetrical Phenonium Ions.
J Am Chem Soc
; 142(18): 8090-8096, 2020 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32314923
4.
Enantioselective C2-Alkylation of Indoles through a Redox-Relay Heck Reaction of 2-Indole Triflates.
Chemistry
; 25(2): 512-515, 2019 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30402891
5.
Palladium-Catalyzed Enantioselective Intermolecular Coupling of Phenols and Allylic Alcohols.
J Am Chem Soc
; 138(49): 15881-15884, 2016 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-27960316
6.
Aziridine Opening via a Phenonium Ion Enables Synthesis of Complex Phenethylamine Derivatives.
Org Lett
; 24(2): 501-505, 2022 01 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34967220
7.
Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles.
Chem Sci
; 8(8): 5248-5260, 2017 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28959424
8.
Enantioselective Narasaka-Heck cyclizations: synthesis of tetrasubstituted nitrogen-bearing stereocenters.
Chem Sci
; 8(3): 1981-1985, 2017 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28451314
9.
Dichotomous mechanistic behavior in Narasaka-Heck cyclizations: electron rich Pd-catalysts generate iminyl radicals.
Chem Sci
; 7(2): 1508-1513, 2016 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29899895
10.
Palladium catalyzed cyclizations of oxime esters with 1,2-disubstituted alkenes: synthesis of dihydropyrroles.
Org Lett
; 15(17): 4616-9, 2013 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23981032
11.
Substituted pyrroles via olefin cross-metathesis.
Org Lett
; 12(18): 4094-7, 2010 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-20712303