Thiago Barcellos, PH.D
Affiliations: | University of Caxias do Sul |
Area:
Organic Synthesis, BiocatalysisGoogle:
"Thiago Barcellos"Mean distance: 8.21 | S | N | B | C | P |
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Publications
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| Hellwig PS, Barcellos AM, Cargnelutti R, et al. (2022) Synthesis of Chalcogenylchromenes through Cyclization of Propargylic Aryl Ethers. The Journal of Organic Chemistry. 87: 15050-15060 |
| Perin G, Peglow TJ, Penteado F, et al. (2022) UVA Light-promoted Catalyst-free Cyclization of Vinyl Selenides: Green and Efficient Synthesis of C3-Unsubstituted 2-Selanyl Benzochalcogenophenes. Chemistry, An Asian Journal. 17: e202101394 |
| Goulart HA, Neto JSS, Barcellos AM, et al. (2021) Synthesis of 4-Selanyl- and 4-Tellanyl-1-isochromen-1-ones Promoted by Diorganyl Dichalcogenides and Oxone. The Journal of Organic Chemistry |
| Manera C, Perondi D, Barbieri RA, et al. (2020) Ultrasonication-promoted synthesis of Ni/mayenite for catalytic reforming of biomass tar. Ultrasonics Sonochemistry. 67: 105165 |
| Belladona AL, Cervo R, Alves D, et al. (2020) C H functionalization of (hetero)arenes: Direct selanylation mediated by Selectfluor Tetrahedron Letters. 61: 152035 |
| Lopes EF, Penteado F, Thurow S, et al. (2019) Synthesis of isoxazolines by the electrophilic chalcogenation of β,γ-unsaturated oximes: fishing novel anti-inflammatory agents. The Journal of Organic Chemistry |
| Peglow TJ, Costa GPD, Duarte LFB, et al. (2019) Ultrasound-Promoted One-Pot Synthesis of Mono- or Bis-Substituted Organylselanyl Pyrroles. The Journal of Organic Chemistry |
| Perin G, Nobre P, Mailahn D, et al. (2019) Synthesis of 4-Organoselanyl-1H-pyrazoles: Oxone®-Mediated Electrophilic Cyclization of α,β-Alkynyl Hydrazones by Using Diorganyl Diselenides Synthesis. 51: 2293-2304 |
| Stach G, Peglow TJ, Roehrs JA, et al. (2019) Synthesis of 2-(Arylselanyl)benzo[b]chalcogenophenes via Intramolecular Cyclization of Vinyl Selenides Synthesis. 51: 578-586 |
| Sacramento Md, Menezes L, Goldani B, et al. (2019) Synthesis of alkynyltellurides mediated by K3PO4 and DMSO New Journal of Chemistry. 43: 11091-11098 |