Detalhe da pesquisa
1.
Recent Strategies in the Nucleophilic Dearomatization of Pyridines, Quinolines, and Isoquinolines.
Chem Rev
; 124(3): 1122-1246, 2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38166390
2.
Two Decades of Progress in the Asymmetric Intramolecular aza-Michael Reaction.
Chem Rec
; 22(1): e202100161, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34415097
3.
Double asymmetric intramolecular aza-Michael reaction: a convenient strategy for the synthesis of quinolizidine alkaloids.
Org Biomol Chem
; 19(40): 8740-8745, 2021 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34581390
4.
Tandem Organocatalytic Cycloaromatization/Intramolecular Friedel-Crafts Alkylation Sequence for the Synthesis of Indolizinones and Pyrrolo-azepinone Derivatives.
J Org Chem
; 84(17): 10785-10795, 2019 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31329441
5.
Synthesis of substituted piperidines by enantioselective desymmetrizing intramolecular aza-Michael reactions.
Org Biomol Chem
; 16(25): 4650-4658, 2018 07 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29911720
6.
Intramolecular Nitrone Cycloaddition of α-(Trifluoromethyl)styrenes. Role of the CF3 Group in the Regioselectivity.
J Org Chem
; 82(5): 2505-2514, 2017 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28186780
7.
Gold-Catalyzed Povarov-Type Reaction of Fluorinated Imino Esters and Furans.
J Org Chem
; 81(15): 6515-24, 2016 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27391192
8.
Gold-catalyzed tandem hydroamination/formal aza-Diels-Alder reaction of homopropargyl amino esters: a combined computational and experimental mechanistic study.
Chemistry
; 21(14): 5459-66, 2015 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-25703591
9.
A Versatile Approach to CF3 -Containing 2-Pyrrolidones by Tandem Michael Addition-Cyclization: Exemplification in the Synthesis of Amidine Class BACE1 Inhibitors.
Chemistry
; 21(33): 11719-26, 2015 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26140617
10.
A general overview of the organocatalytic intramolecular aza-Michael reaction.
Chem Soc Rev
; 43(21): 7430-53, 2014 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25130599
11.
Tandem cross enyne metathesis (CEYM)-intramolecular Diels-Alder reaction (IMDAR). An easy entry to linear bicyclic scaffolds.
Beilstein J Org Chem
; 11: 1486-93, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26425205
12.
Microwave-assisted tandem organocatalytic peptide-coupling intramolecular aza-Michael reaction: α,ß-unsaturated N-acyl pyrazoles as Michael acceptors.
Chemistry
; 20(48): 15697-701, 2014 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-25336358
13.
Tandem gold self-relay catalysis for the synthesis of 2,3-dihydropyridin-4(1 H)-ones: combination of σ and π Lewis acid properties of gold salts.
Chemistry
; 20(43): 14126-31, 2014 Oct 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25196237
14.
Diastereoselective synthesis of 2-phenyl-3-(trifluoromethyl)piperazines as building blocks for drug discovery.
J Org Chem
; 79(12): 5887-94, 2014 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-24856203
15.
One-pot cross-enyne metathesis (CEYM)-Diels-Alder reaction of gem-difluoropropargylic alkynes.
Beilstein J Org Chem
; 9: 2688-95, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24367434
16.
Enantioselective Synthesis of Fluorinated Indolizidinone Derivatives.
Org Lett
; 25(18): 3222-3227, 2023 May 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37125898
17.
Synthesis of 3,4-Dihydropyrimidin(thio)one Containing Scaffold: Biginelli-like Reactions.
Pharmaceuticals (Basel)
; 15(8)2022 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36015096
18.
Microwave-assisted organocatalytic enantioselective intramolecular aza-Michael reaction with α,ß-unsaturated ketones.
Chemistry
; 17(50): 14267-72, 2011 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22083999
19.
Asymmetric synthesis of quaternary α-amino acid derivatives and their fluorinated analogues.
Amino Acids
; 41(3): 559-73, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21424810
20.
Fluorine in pharmaceutical industry: fluorine-containing drugs introduced to the market in the last decade (2001-2011).
Chem Rev
; 114(4): 2432-506, 2014 Feb 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24299176