Detalhe da pesquisa
1.
Fluorimetric Detection of Insulin Misfolding by Probes Derived from Functionalized Fluorene Frameworks.
Molecules
; 29(6)2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38542833
2.
Structure-Antitumor Activity Relationships of Aza- and Diaza-Anthracene-2,9,10-Triones and Their Partially Saturated Derivatives.
Molecules
; 29(2)2024 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38257402
3.
Rapid Assembly of Functionalized 2H-Chromenes and 1,2-Dihydroquinolines via Microwave-Assisted Secondary Amine-Catalyzed Cascade Annulation of 2-O/N-Propargylarylaldehydes with 2,6-Dialkylphenols.
J Org Chem
; 88(16): 11778-11792, 2023 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37556760
4.
m-Terphenylamines, Acting as Selective COX-1 Inhibitors, Block Microglia Inflammatory Response and Exert Neuroprotective Activity.
Molecules
; 28(14)2023 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37513247
5.
Enantioselective catalytic Povarov reactions.
Org Biomol Chem
; 20(8): 1550-1581, 2022 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34994760
6.
Approaches to the Potential Therapy of COVID-19: A General Overview from the Medicinal Chemistry Perspective.
Molecules
; 27(3)2022 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35163923
7.
Mechanochemical Synthesis of Primary Amides.
J Org Chem
; 86(20): 14232-14237, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34596412
8.
Progress in the Chemistry of Tetrahydroquinolines.
Chem Rev
; 119(8): 5057-5191, 2019 04 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30963764
9.
Mechanochemical Aza-Vinylogous Povarov Reactions for the Synthesis of Highly Functionalized 1,2,3,4-Tetrahydroquinolines and 1,2,3,4-Tetrahydro-1,5-Naphthyridines.
Molecules
; 26(5)2021 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33801330
10.
Synthesis of 1,4-Diazepanes and Benzo[b][1,4]diazepines by a Domino Process Involving the In Situ Generation of an Aza-Nazarov Reagent.
J Org Chem
; 85(18): 11924-11933, 2020 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32820631
11.
Sustainable Access to Acridin-9-(10H)ones with an Embedded m-Terphenyl Moiety Based on a Three-Component Reaction.
Molecules
; 25(23)2020 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33260917
12.
Heterogeneous Amberlyst-15-catalyzed synthesis of complex hybrid heterocycles containing [1,6]-naphthyridine under metal-free green conditions.
Org Biomol Chem
; 17(28): 6872-6879, 2019 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31268090
13.
Spirooxindole-pyrrolidine heterocyclic hybrids promotes apoptosis through activation of caspase-3.
Bioorg Med Chem
; 27(12): 2487-2498, 2019 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30853330
14.
Chiral separation of novel iminonaringenin derivatives.
Chirality
; 30(4): 484-490, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29334407
15.
Multicomponent Domino Synthesis, Anticancer Activity and Molecular Modeling Simulation of Complex Dispirooxindolopyrrolidines.
Molecules
; 23(5)2018 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29734741
16.
Mild and General Synthesis of Pyrrolo[2,1-a]isoquinolines and Related Polyheterocyclic Frameworks from Pyrrole Precursors Derived from a Mechanochemical Multicomponent Reaction.
J Org Chem
; 82(5): 2570-2578, 2017 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28186415
17.
One-Pot Synthesis of Functionalized Carbazoles via a CAN-Catalyzed Multicomponent Process Comprising a C-H Activation Step.
J Org Chem
; 82(14): 7492-7502, 2017 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-28636375
18.
High-speed vibration-milling-promoted synthesis of symmetrical frameworks containing two or three pyrrole units.
Beilstein J Org Chem
; 13: 1957-1962, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29062414
19.
Synthesis of 5,6-Dihydrodibenzo[b,h][1,6]naphthyridines via Copper Bromide Catalyzed Intramolecular [4 + 2] Hetero-Diels-Alder Reactions.
J Org Chem
; 81(3): 1116-24, 2016 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26694659
20.
Synthesis of 6,12-Epiminodibenzo[b,f][1,5]diazocines via an Ytterbium Triflate-Catalyzed, AB2 Three-Component Reaction.
J Org Chem
; 81(20): 9687-9694, 2016 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-27682636