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Artigo de periodico
Theoretical approach towards benzodithiophene-based chromophores with extended acceptors for prediction of efficient nonlinear optical behaviour (2024)
Khalid, Muhammad ; Maqsood, Rabia; Shafiq, Iqra ; Baby, Rabia ; Asghar, Muhammad Adnan ; Ahmed, Sarfraz ; Alshehri, Saad M ; Braga, Ataualpa Albert Carmo
Source: Arabian Journal for Science and Engineering. Unidade: IQ
Assunto: QUÍMICA QUÂNTICA
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ABNT
KHALID, Muhammad et al. Theoretical approach towards benzodithiophene-based chromophores with extended acceptors for prediction of efficient nonlinear optical behaviour. Arabian Journal for Science and Engineering, v. 49, p. 339–359, 2024Tradução . . Disponível em: https://doi.org/10.1007/s13369-023-08136-6. Acesso em: 08 jul. 2024.
APA
Khalid, M., Maqsood, R., Shafiq, I., Baby, R., Asghar, M. A., Ahmed, S., et al. (2024). Theoretical approach towards benzodithiophene-based chromophores with extended acceptors for prediction of efficient nonlinear optical behaviour. Arabian Journal for Science and Engineering, 49, 339–359. doi:10.1007/s13369-023-08136-6
NLM
Khalid M, Maqsood R, Shafiq I, Baby R, Asghar MA, Ahmed S, Alshehri SM, Braga AAC. Theoretical approach towards benzodithiophene-based chromophores with extended acceptors for prediction of efficient nonlinear optical behaviour [Internet]. Arabian Journal for Science and Engineering. 2024 ; 49 339–359.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1007/s13369-023-08136-6
Vancouver
Khalid M, Maqsood R, Shafiq I, Baby R, Asghar MA, Ahmed S, Alshehri SM, Braga AAC. Theoretical approach towards benzodithiophene-based chromophores with extended acceptors for prediction of efficient nonlinear optical behaviour [Internet]. Arabian Journal for Science and Engineering. 2024 ; 49 339–359.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1007/s13369-023-08136-6
Artigo de periodico
Influence of azacycle donor moieties on the photovoltaic properties of benzo[c][1,2,5]thiadiazole based organic systems: a DFT study (2023)
shafq, Iqra; Khalid, Muhammad; Asghar, Muhammad Adnan ; Baby, Rabia ; Braga, Ataualpa Albert Carmo ; Alshehri, Saad M; Ahmed, Sarfraz
Source: Scientifc Reports. Unidade: IQ
Subjects: MATERIAIS, ÓPTICA, FOTÔNICA
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ABNT
SHAFQ, Iqra et al. Influence of azacycle donor moieties on the photovoltaic properties of benzo[c][1,2,5]thiadiazole based organic systems: a DFT study. Scientifc Reports, v. 13, p. 1-12 art. 14630, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41598-023-41679-0. Acesso em: 08 jul. 2024.
APA
shafq, I., Khalid, M., Asghar, M. A., Baby, R., Braga, A. A. C., Alshehri, S. M., & Ahmed, S. (2023). Influence of azacycle donor moieties on the photovoltaic properties of benzo[c][1,2,5]thiadiazole based organic systems: a DFT study. Scientifc Reports, 13, 1-12 art. 14630. doi:10.1038/s41598-023-41679-0
NLM
shafq I, Khalid M, Asghar MA, Baby R, Braga AAC, Alshehri SM, Ahmed S. Influence of azacycle donor moieties on the photovoltaic properties of benzo[c][1,2,5]thiadiazole based organic systems: a DFT study [Internet]. Scientifc Reports. 2023 ; 13 1-12 art. 14630.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-023-41679-0
Vancouver
shafq I, Khalid M, Asghar MA, Baby R, Braga AAC, Alshehri SM, Ahmed S. Influence of azacycle donor moieties on the photovoltaic properties of benzo[c][1,2,5]thiadiazole based organic systems: a DFT study [Internet]. Scientifc Reports. 2023 ; 13 1-12 art. 14630.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-023-41679-0
Artigo de periodico
Experimental and quantum chemical studies of hydrazone-based organic chromophores: synthesis, spectroscopic and nonlinear optical properties (2023)
Haroon, Muhammad ; Akhtar, Tashfeen ; Khalid, Muhammad ; Mehmood, Hasnain; Braga, Ataualpa Albert Carmo ; Alhokbany, Norah ; Ahmed, Sarfraz
Source: ChemistrySelect. Unidade: IQ
Subjects: ESPECTROSCOPIA, MATERIAIS ÓPTICOS
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ABNT
HAROON, Muhammad et al. Experimental and quantum chemical studies of hydrazone-based organic chromophores: synthesis, spectroscopic and nonlinear optical properties. ChemistrySelect, v. 8, n. 28, p. 1-11, 2023Tradução . . Disponível em: https://doi.org/10.1002/slct.202301209. Acesso em: 08 jul. 2024.
APA
Haroon, M., Akhtar, T., Khalid, M., Mehmood, H., Braga, A. A. C., Alhokbany, N., & Ahmed, S. (2023). Experimental and quantum chemical studies of hydrazone-based organic chromophores: synthesis, spectroscopic and nonlinear optical properties. ChemistrySelect, 8( 28), 1-11. doi:10.1002/slct.202301209
NLM
Haroon M, Akhtar T, Khalid M, Mehmood H, Braga AAC, Alhokbany N, Ahmed S. Experimental and quantum chemical studies of hydrazone-based organic chromophores: synthesis, spectroscopic and nonlinear optical properties [Internet]. ChemistrySelect. 2023 ; 8( 28): 1-11.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.202301209
Vancouver
Haroon M, Akhtar T, Khalid M, Mehmood H, Braga AAC, Alhokbany N, Ahmed S. Experimental and quantum chemical studies of hydrazone-based organic chromophores: synthesis, spectroscopic and nonlinear optical properties [Internet]. ChemistrySelect. 2023 ; 8( 28): 1-11.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.202301209
Artigo de periodico
Promising impact of push–pull configuration into designed octacyclic naphthalene-based organic scaffolds for nonlinear optical amplitudes: a quantum chemical approach (2023)
Khalid, Muhammad; Shafiq, Iqra; Asghar, Muhammad Adnan; Braga, Ataualpa Albert Carmo ; Alshehri, Saad M; Haroon, Muhammad; Sanyang, Muhammed Lamin
Source: Scientific Reports. Unidade: IQ
Subjects: QUÍMICA QUÂNTICA, MATERIAIS ÓPTICOS
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ABNT
KHALID, Muhammad et al. Promising impact of push–pull configuration into designed octacyclic naphthalene-based organic scaffolds for nonlinear optical amplitudes: a quantum chemical approach. Scientific Reports, v. 13, p. 1-16 art. 20104, 2023Tradução . . Disponível em: https://dx.doi.org/10.1038/s41598-023-44327-9. Acesso em: 08 jul. 2024.
APA
Khalid, M., Shafiq, I., Asghar, M. A., Braga, A. A. C., Alshehri, S. M., Haroon, M., & Sanyang, M. L. (2023). Promising impact of push–pull configuration into designed octacyclic naphthalene-based organic scaffolds for nonlinear optical amplitudes: a quantum chemical approach. Scientific Reports, 13, 1-16 art. 20104. doi:10.1038/s41598-023-44327-9
NLM
Khalid M, Shafiq I, Asghar MA, Braga AAC, Alshehri SM, Haroon M, Sanyang ML. Promising impact of push–pull configuration into designed octacyclic naphthalene-based organic scaffolds for nonlinear optical amplitudes: a quantum chemical approach [Internet]. Scientific Reports. 2023 ; 13 1-16 art. 20104.[citado 2024 jul. 08 ] Available from: https://dx.doi.org/10.1038/s41598-023-44327-9
Vancouver
Khalid M, Shafiq I, Asghar MA, Braga AAC, Alshehri SM, Haroon M, Sanyang ML. Promising impact of push–pull configuration into designed octacyclic naphthalene-based organic scaffolds for nonlinear optical amplitudes: a quantum chemical approach [Internet]. Scientific Reports. 2023 ; 13 1-16 art. 20104.[citado 2024 jul. 08 ] Available from: https://dx.doi.org/10.1038/s41598-023-44327-9
Artigo de periodico
First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores (2022)
Khalid, Muhammad; Ahmed, Rameez; shafq, Iqra; Arshad, Muhammad; Asghar, Muhammad Adnan; Munawar, Khurram Shahzad ; Imran, Muhammad; Braga, Ataualpa Albert Carmo
Source: Scientifc Reports. Unidades: FM, IQ
Subjects: CÉLULAS SOLARES, DEPÓSITOS DE COMBUSTÍVEL FÓSSIL
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ABNT
KHALID, Muhammad et al. First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores. Scientifc Reports, v. 12, p. 1-15 art. 20148 , 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-24087-8. Acesso em: 08 jul. 2024.
APA
Khalid, M., Ahmed, R., shafq, I., Arshad, M., Asghar, M. A., Munawar, K. S., et al. (2022). First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores. Scientifc Reports, 12, 1-15 art. 20148 . doi:10.1038/s41598-022-24087-8
NLM
Khalid M, Ahmed R, shafq I, Arshad M, Asghar MA, Munawar KS, Imran M, Braga AAC. First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores [Internet]. Scientifc Reports. 2022 ; 12 1-15 art. 20148 .[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-022-24087-8
Vancouver
Khalid M, Ahmed R, shafq I, Arshad M, Asghar MA, Munawar KS, Imran M, Braga AAC. First theoretical framework for highly efficient photovoltaic parameters by structural modification with benzothiophene-incorporated acceptors in dithiophene based chromophores [Internet]. Scientifc Reports. 2022 ; 12 1-15 art. 20148 .[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-022-24087-8
Artigo de periodico
Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies (2022)
Basri, Rabia ; Khalid, Muhammad ; Khan, Muhammad Usman; Abdullah, Muhammad; Syed, Asad; Elgorban, Abdallah M ; Al-Rejaie, Salim S ; Braga, Ataualpa Albert Carmo ; Shafiq, Zahid
Source: Scientific Reports. Unidade: IQ
Subjects: COLORIMETRIA, FLÚOR, ÍONS
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ABNT
BASRI, Rabia et al. Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies. Scientific Reports, v. 12, p. 1-19, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-08860-3. Acesso em: 08 jul. 2024.
APA
Basri, R., Khalid, M., Khan, M. U., Abdullah, M., Syed, A., Elgorban, A. M., et al. (2022). Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies. Scientific Reports, 12, 1-19. doi:10.1038/s41598-022-08860-3
NLM
Basri R, Khalid M, Khan MU, Abdullah M, Syed A, Elgorban AM, Al-Rejaie SS, Braga AAC, Shafiq Z. Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies [Internet]. Scientific Reports. 2022 ; 12 1-19.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-022-08860-3
Vancouver
Basri R, Khalid M, Khan MU, Abdullah M, Syed A, Elgorban AM, Al-Rejaie SS, Braga AAC, Shafiq Z. Quinoline based thiosemicarbazones as colorimetric chemosensors for fluoride and cyanide ions and DFT studies [Internet]. Scientific Reports. 2022 ; 12 1-19.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-022-08860-3
Artigo de periodico
Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams (2022)
Braga, Ingredy Bastos; Angnes, Ricardo Almir ; Lucca Júnior, Emílio Carlos de; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: European Journal of Organic Chemistry. Unidade: IQ
Subjects: PRODUTOS NATURAIS, LIGANTES
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ABNT
BRAGA, Ingredy Bastos et al. Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams. European Journal of Organic Chemistry, v. 26, n. 39, p. 1-8, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200377. Acesso em: 08 jul. 2024.
APA
Braga, I. B., Angnes, R. A., Lucca Júnior, E. C. de, Braga, A. A. C., & Correia, C. R. D. (2022). Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams. European Journal of Organic Chemistry, 26( 39), 1-8. doi:10.1002/ejoc.202200377
NLM
Braga IB, Angnes RA, Lucca Júnior EC de, Braga AAC, Correia CRD. Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams [Internet]. European Journal of Organic Chemistry. 2022 ; 26( 39): 1-8.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/ejoc.202200377
Vancouver
Braga IB, Angnes RA, Lucca Júnior EC de, Braga AAC, Correia CRD. Enantioselective synthesis of alpha,beta-unsaturated aryl lactams by heck-matsuda and heck-Mizoroki Arylations of Enelactams [Internet]. European Journal of Organic Chemistry. 2022 ; 26( 39): 1-8.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/ejoc.202200377
Artigo de periodico
Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids (2022)
Ali, Akbar ; Khalid, Muhammad; Ashfaq, Muhammad; Malik, Abida Naseem; Muhammad Nawaz Tahir; Assiri, Mohammed A; Imran, Muhammad; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo
Source: ChemistrySelect. Unidade: IQ
Subjects: DOENÇAS INFECCIOSAS, MALÁRIA, SAIS, QUÍMICA ORGÂNICA, QUÍMICA SUPRAMOLECULAR
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ABNT
ALI, Akbar et al. Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids. ChemistrySelect, v. 7, p. 1-13 art. e202200349, 2022Tradução . . Disponível em: https://doi.org/10.1002/slct.202200349. Acesso em: 08 jul. 2024.
APA
Ali, A., Khalid, M., Ashfaq, M., Malik, A. N., Muhammad Nawaz Tahir,, Assiri, M. A., et al. (2022). Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids. ChemistrySelect, 7, 1-13 art. e202200349. doi:10.1002/slct.202200349
NLM
Ali A, Khalid M, Ashfaq M, Malik AN, Muhammad Nawaz Tahir, Assiri MA, Imran M, Morais SF de A, Braga AAC. Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids [Internet]. ChemistrySelect. 2022 ; 7 1-13 art. e202200349.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.202200349
Vancouver
Ali A, Khalid M, Ashfaq M, Malik AN, Muhammad Nawaz Tahir, Assiri MA, Imran M, Morais SF de A, Braga AAC. Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids [Internet]. ChemistrySelect. 2022 ; 7 1-13 art. e202200349.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.202200349
Artigo de periodico
2-Nitro- and 4-fluorocinnamaldehyde based receptors as naked-eye chemosensors to potential molecular keypad lock (2021)
Islam, Muhammad; Shafiq, Zahid ; Mabood, Fazal; Shah, Hakikulla H; Singh, Vandita; Khalid, Muhammad ; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo ; Khan, Muhammad Usman ; Hussain, Javid; Al-Harrasi, Ahmed; Marraiki, Najat; Zaghloul, Nouf S. S
Source: Scientific Reports. Unidade: IQ
Subjects: RECEPTORES, MOLÉCULA
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ABNT
ISLAM, Muhammad et al. 2-Nitro- and 4-fluorocinnamaldehyde based receptors as naked-eye chemosensors to potential molecular keypad lock. Scientific Reports, v. 11, p. 1-24 art. 20847, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-99599-w. Acesso em: 08 jul. 2024.
APA
Islam, M., Shafiq, Z., Mabood, F., Shah, H. H., Singh, V., Khalid, M., et al. (2021). 2-Nitro- and 4-fluorocinnamaldehyde based receptors as naked-eye chemosensors to potential molecular keypad lock. Scientific Reports, 11, 1-24 art. 20847. doi:10.1038/s41598-021-99599-w
NLM
Islam M, Shafiq Z, Mabood F, Shah HH, Singh V, Khalid M, Morais SF de A, Braga AAC, Khan MU, Hussain J, Al-Harrasi A, Marraiki N, Zaghloul NSS. 2-Nitro- and 4-fluorocinnamaldehyde based receptors as naked-eye chemosensors to potential molecular keypad lock [Internet]. Scientific Reports. 2021 ; 11 1-24 art. 20847.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-021-99599-w
Vancouver
Islam M, Shafiq Z, Mabood F, Shah HH, Singh V, Khalid M, Morais SF de A, Braga AAC, Khan MU, Hussain J, Al-Harrasi A, Marraiki N, Zaghloul NSS. 2-Nitro- and 4-fluorocinnamaldehyde based receptors as naked-eye chemosensors to potential molecular keypad lock [Internet]. Scientific Reports. 2021 ; 11 1-24 art. 20847.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-021-99599-w
Artigo de periodico
Molecular engineering of indenoindene-3-ethylrodanine acceptors with A2-A1-D-A1-A2 architecture for promising fullerene-free organic solar cells (2021)
Khalid, Muhammad ; Momina; Imran, Muhammad; Rehman, Muhammad Fayyaz ur ; Braga, Ataualpa Albert Carmo ; Akram, Muhammad Safwan
Source: Scientific Reports. Unidade: IQ
Subjects: CÉLULAS SOLARES, ENERGIA SOLAR
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ABNT
KHALID, Muhammad et al. Molecular engineering of indenoindene-3-ethylrodanine acceptors with A2-A1-D-A1-A2 architecture for promising fullerene-free organic solar cells. Scientific Reports, v. 11, p. 1-15 art. 20320, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-99308-7. Acesso em: 08 jul. 2024.
APA
Khalid, M., Momina,, Imran, M., Rehman, M. F. ur, Braga, A. A. C., & Akram, M. S. (2021). Molecular engineering of indenoindene-3-ethylrodanine acceptors with A2-A1-D-A1-A2 architecture for promising fullerene-free organic solar cells. Scientific Reports, 11, 1-15 art. 20320. doi:10.1038/s41598-021-99308-7
NLM
Khalid M, Momina, Imran M, Rehman MF ur, Braga AAC, Akram MS. Molecular engineering of indenoindene-3-ethylrodanine acceptors with A2-A1-D-A1-A2 architecture for promising fullerene-free organic solar cells [Internet]. Scientific Reports. 2021 ; 11 1-15 art. 20320.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-021-99308-7
Vancouver
Khalid M, Momina, Imran M, Rehman MF ur, Braga AAC, Akram MS. Molecular engineering of indenoindene-3-ethylrodanine acceptors with A2-A1-D-A1-A2 architecture for promising fullerene-free organic solar cells [Internet]. Scientific Reports. 2021 ; 11 1-15 art. 20320.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-021-99308-7
Artigo de periodico
Exploration of promising optical and electronic properties of (non-polymer) small donor molecules for organic solar cells (2021)
Khalid, Muhammad ; Khan, Muhammad Usman ; Ahmed, Saeed; Shafiq, Zahid ; Alam, Mohammed Mujahid; Imran, Muhammad; Braga, Ataualpa Albert Carmo ; Akram, Muhammad Safwan
Source: Scientific Reports. Unidade: IQ
Subjects: CÉLULAS SOLARES, COMPOSTOS ORGÂNICOS
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ABNT
KHALID, Muhammad et al. Exploration of promising optical and electronic properties of (non-polymer) small donor molecules for organic solar cells. Scientific Reports, v. 11, p. 1-15 art. 21540, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-01070-3. Acesso em: 08 jul. 2024.
APA
Khalid, M., Khan, M. U., Ahmed, S., Shafiq, Z., Alam, M. M., Imran, M., et al. (2021). Exploration of promising optical and electronic properties of (non-polymer) small donor molecules for organic solar cells. Scientific Reports, 11, 1-15 art. 21540. doi:10.1038/s41598-021-01070-3
NLM
Khalid M, Khan MU, Ahmed S, Shafiq Z, Alam MM, Imran M, Braga AAC, Akram MS. Exploration of promising optical and electronic properties of (non-polymer) small donor molecules for organic solar cells [Internet]. Scientific Reports. 2021 ; 11 1-15 art. 21540.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-021-01070-3
Vancouver
Khalid M, Khan MU, Ahmed S, Shafiq Z, Alam MM, Imran M, Braga AAC, Akram MS. Exploration of promising optical and electronic properties of (non-polymer) small donor molecules for organic solar cells [Internet]. Scientific Reports. 2021 ; 11 1-15 art. 21540.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1038/s41598-021-01070-3
Artigo de periodico
Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity (2020)
Polo, Ellen Christine; Wang, Martí Fernández; Angnes, Ricardo Almir; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: Advanced Synthesis and Catalysis. Unidade: IQ
Subjects: CATÁLISE ASSIMÉTRICA, REAÇÕES QUÍMICAS, PALÁDIO
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ABNT
POLO, Ellen Christine et al. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, v. 362, p. 884 – 892, 2020Tradução . . Disponível em: https://doi.org/10.1002/adsc.201901471. Acesso em: 08 jul. 2024.
APA
Polo, E. C., Wang, M. F., Angnes, R. A., Braga, A. A. C., & Correia, C. R. D. (2020). Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, 362, 884 – 892. doi:10.1002/adsc.201901471
NLM
Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/adsc.201901471
Vancouver
Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/adsc.201901471
Artigo de periodico
On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug (2019)
Rocha, Júlio César da ; Sihn, Luca Michael ; Uchiyama, Mayara Klimuk ; Ribeiro, Marcos A; Franco, Maurício Portiolli ; Braga, Ataualpa Albert Carmo ; Silveira Junior, Alceu Totti ; Toma, Henrique Eisi
Source: ChemistrySelect. Unidade: IQ
Subjects: MEDICAMENTO, OSTEOPOROSE
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ABNT
ROCHA, Júlio César da et al. On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug. ChemistrySelect, v. 4, p. 13926-13931, 2019Tradução . . Disponível em: https://doi.org/10.1002/slct.201904149. Acesso em: 08 jul. 2024.
APA
Rocha, J. C. da, Sihn, L. M., Uchiyama, M. K., Ribeiro, M. A., Franco, M. P., Braga, A. A. C., et al. (2019). On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug. ChemistrySelect, 4, 13926-13931. doi:10.1002/slct.201904149
NLM
Rocha JC da, Sihn LM, Uchiyama MK, Ribeiro MA, Franco MP, Braga AAC, Silveira Junior AT, Toma HE. On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug [Internet]. ChemistrySelect. 2019 ; 4 13926-13931.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.201904149
Vancouver
Rocha JC da, Sihn LM, Uchiyama MK, Ribeiro MA, Franco MP, Braga AAC, Silveira Junior AT, Toma HE. On the amazing reactivity of the ranelate lon: new applications of an old antiosporotic drug [Internet]. ChemistrySelect. 2019 ; 4 13926-13931.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.201904149
Artigo de periodico
Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins (2018)
Oliveira, Juliana Manso de; Angnes, Ricardo Almir; Khan, Ismat Ullah; Polo, Ellen Christine; Heerdt, Gabriel; Servilha, Bruno M; Silva, Vitor H. Menezes da; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte
Source: Chemistry European Journal. Unidade: IQ
Subjects: CATÁLISE, PALÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Juliana Manso de et al. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, v. 24, n. 45, p. 11738-11747, 2018Tradução . . Disponível em: https://doi.org/10.1002/chem.201801910. Acesso em: 08 jul. 2024.
APA
Oliveira, J. M. de, Angnes, R. A., Khan, I. U., Polo, E. C., Heerdt, G., Servilha, B. M., et al. (2018). Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, 24( 45), 11738-11747. doi:10.1002/chem.201801910
NLM
Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/chem.201801910
Vancouver
Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/chem.201801910
Artigo de periodico
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 08 jul. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/ajoc.201700154
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/ajoc.201700154
Artigo de periodico
Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations (2016)
Silva, Vitor Hugo Menezes da; Silva Junior, Luiz Fernando da; Braga, Ataualpa Albert Carmo
Source: ChemistrySelect. Unidade: IQ
Subjects: FÍSICO-QUÍMICA, SOLVENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Vitor Hugo Menezes da e SILVA JUNIOR, Luiz Fernando da e BRAGA, Ataualpa Albert Carmo. Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations. ChemistrySelect, v. 1, p. 2706-2711, 2016Tradução . . Disponível em: https://doi.org/10.1002/slct.201600228. Acesso em: 08 jul. 2024.
APA
Silva, V. H. M. da, Silva Junior, L. F. da, & Braga, A. A. C. (2016). Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations. ChemistrySelect, 1, 2706-2711. doi:10.1002/slct.201600228
NLM
Silva VHM da, Silva Junior LF da, Braga AAC. Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations [Internet]. ChemistrySelect. 2016 ; 1 2706-2711.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.201600228
Vancouver
Silva VHM da, Silva Junior LF da, Braga AAC. Iodine(III)-mediated ring contraction of1,2-Dihydronaphthalenes: mechanistic insight byComputational investigations [Internet]. ChemistrySelect. 2016 ; 1 2706-2711.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/slct.201600228
Parte de monografia/livro
Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*) (2016)
Santos, Marilia Silva; Correia, José Tiago Menezes; Batista, Ana Paula de Lima; Rodrigues Junior, Manoel Trindade; Braga, Ataualpa Albert Carmo ; Eberlin, Marcos Nogueira; Coelho, Fernando
Source: Lewis base catalysis in organic synthesis. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Marilia Silva et al. Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*). Lewis base catalysis in organic synthesis. Tradução . Weinheim: Wiley-VCH Verlag, 2016. . Disponível em: https://doi.org/10.1002/9783527675142.ch7. Acesso em: 08 jul. 2024.
APA
Santos, M. S., Correia, J. T. M., Batista, A. P. de L., Rodrigues Junior, M. T., Braga, A. A. C., Eberlin, M. N., & Coelho, F. (2016). Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*). In Lewis base catalysis in organic synthesis. Weinheim: Wiley-VCH Verlag. doi:10.1002/9783527675142.ch7
NLM
Santos MS, Correia JTM, Batista AP de L, Rodrigues Junior MT, Braga AAC, Eberlin MN, Coelho F. Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*) [Internet]. In: Lewis base catalysis in organic synthesis. Weinheim: Wiley-VCH Verlag; 2016. [citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/9783527675142.ch7
Vancouver
Santos MS, Correia JTM, Batista AP de L, Rodrigues Junior MT, Braga AAC, Eberlin MN, Coelho F. Mechanistic options for the Morita–Baylis–Hillman reaction (n → π*) [Internet]. In: Lewis base catalysis in organic synthesis. Weinheim: Wiley-VCH Verlag; 2016. [citado 2024 jul. 08 ] Available from: https://doi.org/10.1002/9783527675142.ch7
Artigo de periodico
DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction (2016)
Batista, Ana Paula de Lima; Coelho, Fernando; Braga, Ataualpa Albert Carmo
Source: Theoretical Chemistry Accounts. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, CATÁLISE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISTA, Ana Paula de Lima e COELHO, Fernando e BRAGA, Ataualpa Albert Carmo. DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction. Theoretical Chemistry Accounts, v. 135, p. 1-8 art. 186, 2016Tradução . . Disponível em: https://doi.org/10.1007/s00214-016-1946-1. Acesso em: 08 jul. 2024.
APA
Batista, A. P. de L., Coelho, F., & Braga, A. A. C. (2016). DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction. Theoretical Chemistry Accounts, 135, 1-8 art. 186. doi:10.1007/s00214-016-1946-1
NLM
Batista AP de L, Coelho F, Braga AAC. DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction [Internet]. Theoretical Chemistry Accounts. 2016 ; 135 1-8 art. 186.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1007/s00214-016-1946-1
Vancouver
Batista AP de L, Coelho F, Braga AAC. DFT exploration of mechanistic pathways of an aza‑Morita–Baylis–Hillman reaction [Internet]. Theoretical Chemistry Accounts. 2016 ; 135 1-8 art. 186.[citado 2024 jul. 08 ] Available from: https://doi.org/10.1007/s00214-016-1946-1

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