ReP USP - Resultado da busca

Artigo de periodico
Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction (2022)
Darbem, Mariana P; Esteves, Henrique A; Burrow, Robert A ; Paulino, Antonio Augusto Soares ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: RSC Advances. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
DARBEM, Mariana P et al. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, v. 12, p. 2145–2149, 2022Tradução . . Disponível em: https://doi.org/10.1039/d1ra08388k. Acesso em: 27 abr. 2024.
APA
Darbem, M. P., Esteves, H. A., Burrow, R. A., Paulino, A. A. S., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, 12, 2145–2149. doi:10.1039/d1ra08388k
NLM
Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/d1ra08388k
Vancouver
Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/d1ra08388k
Artigo de periodico
α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals (2020)
Darbem, Mariana P; Esteves, Henrique A; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidades: FCF, IQ
Subjects: GLICOSÍDEOS, PALÁDIO
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ABNT
DARBEM, Mariana P et al. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 5220–5226, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000846. Acesso em: 27 abr. 2024.
APA
Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, & Stefani, H. A. (2020). α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 5220–5226. doi:10.1002/ejoc.202000846
NLM
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ejoc.202000846
Vancouver
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ejoc.202000846
Artigo de periodico
Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals (2020)
Darbem, Mariana P; Esteves, Henrique A; Oliveira, Isadora Maria de ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: ChemCatChem. Unidades: BIOTECNOLOGIA, FCF, IQ
Subjects: PALÁDIO, HIDRÓLISE
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ABNT
DARBEM, Mariana P et al. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, v. 12, n. 2, p. 576-583, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.201901403. Acesso em: 27 abr. 2024.
APA
Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, Pimenta, D. C., & Stefani, H. A. (2020). Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, 12( 2), 576-583. doi:10.1002/cctc.201901403
NLM
Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/cctc.201901403
Vancouver
Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/cctc.201901403
Artigo de periodico
Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers (2020)
Oliveira, Isadora Maria de ; Esteves, Henrique A; Darbem, Mariana P; Sartorelli, Arthur; Correra, Thiago Carita ; Oliveira, Andre F. Rodrigues ; Pimenta, Daniel C; Zukerman-Schpector, Júlio ; Stefani, Hélio Alexandre
Source: ChemCatChem. Unidades: FCF, IQ
Subjects: LIGANTES, CATALISADORES
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ABNT
OLIVEIRA, Isadora Maria de et al. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, v. 12, p. 3545–3552, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.202000395. Acesso em: 27 abr. 2024.
APA
Oliveira, I. M. de, Esteves, H. A., Darbem, M. P., Sartorelli, A., Correra, T. C., Oliveira, A. F. R., et al. (2020). Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, 12, 3545–3552. doi:10.1002/cctc.202000395
NLM
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/cctc.202000395
Vancouver
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/cctc.202000395
Artigo de periodico
Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution (2019)
Santos, Fabiano S; Zanotto, Gabriel M; Argomedo, Luiz M. Z; Darbem, Mariana P; Gonçalves, Paulo F. B; Stefani, Hélio Alexandre ; Rodembusch, Fabiano S
Source: Dyes and Pigments. Unidade: FCF
Subjects: SENSORES ÓPTICOS, SÍNTESE ORGÂNICA
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ABNT
SANTOS, Fabiano S et al. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, v. 165, p. 372-382, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.02.047. Acesso em: 27 abr. 2024.
APA
Santos, F. S., Zanotto, G. M., Argomedo, L. M. Z., Darbem, M. P., Gonçalves, P. F. B., Stefani, H. A., & Rodembusch, F. S. (2019). Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, 165, 372-382. doi:10.1016/j.dyepig.2019.02.047
NLM
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
Vancouver
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
Artigo de periodico
Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction (2019)
Darbem, Mariana P; Esteves, C. Henrique A; Oliveira, Isadora M. de; Reis, Joel S; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: RSC Advances. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DARBEM, Mariana P et al. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, v. 9, p. 9468–9474, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9ra00523d. Acesso em: 27 abr. 2024.
APA
Darbem, M. P., Esteves, C. H. A., Oliveira, I. M. de, Reis, J. S., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, 9, 9468–9474. doi:10.1039/c9ra00523d
NLM
Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/c9ra00523d
Vancouver
Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/c9ra00523d
Artigo de periodico
Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides (2019)
Esteves, Henrique A; Darbem, Mariana P; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidades: BIOTECNOLOGIA, FCF
Subjects: MONÓXIDO DE CARBONO, PALÁDIO
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ABNT
ESTEVES, Henrique A et al. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, v. 2019, p. 7384-7388, 2019Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201901081. Acesso em: 27 abr. 2024.
APA
Esteves, H. A., Darbem, M. P., Pimenta, D. C., & Stefani, H. A. (2019). Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, 2019, 7384-7388. doi:10.1002/ejoc.201901081
NLM
Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ejoc.201901081
Vancouver
Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ejoc.201901081
Artigo de periodico
Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source (2019)
Darbem, Mariana P; Kanno, Karina S; Oliveira, Isadora M. de; Esteves, C. Henrique A; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: New Journal of Chemistry. Unidade: FCF
Subjects: MONÓXIDO DE CARBONO, MOLIBDÊNIO
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ABNT
DARBEM, Mariana P et al. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, v. 43, n. 2, p. 696-699, 2019Tradução . . Disponível em: https://doi.org/10.1039/c8nj04540b. Acesso em: 27 abr. 2024.
APA
Darbem, M. P., Kanno, K. S., Oliveira, I. M. de, Esteves, C. H. A., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, 43( 2), 696-699. doi:10.1039/c8nj04540b
NLM
Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/c8nj04540b
Vancouver
Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/c8nj04540b
Artigo de periodico
Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization (2019)
Oliveira, Isadora M. de; Esteves, Carlos Henrique Alves ; Darbem, Mariana P; Pimenta, Daniel Carvalho ; Schpector, Júlio Zukerman ; Ferreira, Antônio Gilberto; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: Advanced Synthesis and Catalysis. Unidade: FCF
Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO
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ABNT
OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 27 abr. 2024.
APA
Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142
NLM
Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/adsc.201900142
Vancouver
Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/adsc.201900142
Artigo de periodico
Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted (2018)
Oliveira, Isadora M. de; Darbem, Mariana P; Esteves, Carlos Henrique Alves; Pimenta, Daniel C; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: Tetrahedron Letters. Unidade: FCF
Subjects: ITÉRBIO, SÍNTESE ORGÂNICA
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, v. 59, n. 24, p. 3907-3911, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.09.022. Acesso em: 27 abr. 2024.
APA
Oliveira, I. M. de, Darbem, M. P., Esteves, C. H. A., Pimenta, D. C., Schpector, J. Z., Stefani, H. A., & Manarin, F. (2018). Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, 59( 24), 3907-3911. doi:10.1016/j.tetlet.2018.09.022
NLM
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Vancouver
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022

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