Detalhe da pesquisa
1.
New Palladacycle-Derived Acylhydrazones as Pre-catalysts in Mirozoki-Heck Coupling and Oxyarylations.
An Acad Bras Cienc;
90(1 Suppl 2): 1273-1278, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29768577
2.
Laboratory-Scale Membrane Reactor for the Generation of Anhydrous Diazomethane.
J Org Chem;
81(14): 5814-23, 2016 07 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27359257
3.
Three-step synthesis of (±)-preussin from decanal.
J Org Chem;
79(14): 6748-53, 2014 Jul 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24979222
4.
Continuous flow synthesis of α-halo ketones: essential building blocks of antiretroviral agents.
J Org Chem;
79(4): 1555-62, 2014 Feb 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24471789
5.
Alkylation of 6-thiopurine derivatives by the Mitsunobu reaction.
Nucleosides Nucleotides Nucleic Acids;
42(7): 516-526, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36593726
6.
Preclinical development of kinetin as a safe error-prone SARS-CoV-2 antiviral able to attenuate virus-induced inflammation.
Nat Commun;
14(1): 199, 2023 01 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36639383
7.
α,ß-Unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids. Total synthesis of 1-deoxy-8,8a-diepicastanospermine and 1,6-dideoxyepicastanospermine and formal synthesis of pumiliotoxin 251D.
J Org Chem;
77(21): 9926-31, 2012 Nov 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23067106
8.
Preparation of α,ß-unsaturated diazoketones employing a Horner-Wadsworth-Emmons reagent.
J Org Chem;
76(1): 289-92, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21155601
9.
Preclinical development of kinetin as a safe error-prone SARS-CoV-2 antiviral able to attenuate virus-induced inflammation
Artigo
em Inglês
| Arca: Repositório institucional da Fiocruz
| ID: arc-56575
10.
SmI2-mediated couplings of α-amino acid derivatives. Formal synthesis of (-)-pumiliotoxin 251D and (±)-epiquinamide.
Org Lett;
15(10): 2434-7, 2013 May 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23639065