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Artigo de periodico
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction (2013)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Vasconcelos, Stanley Nunes Siqueira; Manarin, Flávia; Souza, Frederico B
Source: Tetrahedron Letters. Unidade: FCF
Subjects: TELÚRIO, SÍNTESE ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, v. 54, n. 22, p. 2809-2812, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.03.061. Acesso em: 19 set. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Vasconcelos, S. N. S., Manarin, F., & Souza, F. B. (2013). Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, 54( 22), 2809-2812. doi:10.1016/j.tetlet.2013.03.061
NLM
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
Vancouver
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
Artigo de periodico
Efficient synthesis of chlorohydrins using ClC'H IND.2'MgCl LiCl (2013)
Nishimura, Rodolfo H.; Toledo, Fabiano T.; Lopes, Joao Luis Callegari; Clososki, Giuliano Cesar
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: CLORETO, MAGNÉSIO
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ABNT
NISHIMURA, Rodolfo H. et al. Efficient synthesis of chlorohydrins using ClC'H IND.2'MgCl LiCl. Tetrahedron Letters, v. 54, n. 4, p. 287-290, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.10.132. Acesso em: 19 set. 2024.
APA
Nishimura, R. H., Toledo, F. T., Lopes, J. L. C., & Clososki, G. C. (2013). Efficient synthesis of chlorohydrins using ClC'H IND.2'MgCl LiCl. Tetrahedron Letters, 54( 4), 287-290. doi:10.1016/j.tetlet.2012.10.132
NLM
Nishimura RH, Toledo FT, Lopes JLC, Clososki GC. Efficient synthesis of chlorohydrins using ClC'H IND.2'MgCl LiCl [Internet]. Tetrahedron Letters. 2013 ; 54( 4): 287-290.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.10.132
Vancouver
Nishimura RH, Toledo FT, Lopes JLC, Clososki GC. Efficient synthesis of chlorohydrins using ClC'H IND.2'MgCl LiCl [Internet]. Tetrahedron Letters. 2013 ; 54( 4): 287-290.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.10.132
Artigo de periodico
Biomimetic synthesis of diversifolin (2013)
Sass, Daiane Cristina; Heleno, Vladimir Constantino Gomes; Barbosa, Jader da Silva; Morais, Gustavo Oliveira; Costa, Fernando Batista da; Constantino, Maurício Gomes
Source: Tetrahedron Letters. Unidades: FCFRP, FFCLRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
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ABNT
SASS, Daiane Cristina et al. Biomimetic synthesis of diversifolin. Tetrahedron Letters, v. 54, p. 625-627, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.11.134. Acesso em: 19 set. 2024.
APA
Sass, D. C., Heleno, V. C. G., Barbosa, J. da S., Morais, G. O., Costa, F. B. da, & Constantino, M. G. (2013). Biomimetic synthesis of diversifolin. Tetrahedron Letters, 54, 625-627. doi:10.1016/j.tetlet.2012.11.134
NLM
Sass DC, Heleno VCG, Barbosa J da S, Morais GO, Costa FB da, Constantino MG. Biomimetic synthesis of diversifolin [Internet]. Tetrahedron Letters. 2013 ; 54 625-627.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.11.134
Vancouver
Sass DC, Heleno VCG, Barbosa J da S, Morais GO, Costa FB da, Constantino MG. Biomimetic synthesis of diversifolin [Internet]. Tetrahedron Letters. 2013 ; 54 625-627.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.11.134
Artigo de periodico
One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles (2013)
Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Souza, Frederico B; Manarin, Flávia; Zukerman-Schpector, Júlio
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, v. 54, n. 43, p. 5821-5825, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.064. Acesso em: 19 set. 2024.
APA
Stefani, H. A., Vasconcelos, S. N. S., Souza, F. B., Manarin, F., & Zukerman-Schpector, J. (2013). One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, 54( 43), 5821-5825. doi:10.1016/j.tetlet.2013.08.064
NLM
Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
Vancouver
Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
Artigo de periodico
Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III) (2013)
Ahmad, Anees; Scarassati, Paulo; Jalalian, Nazli; Olofsson, Berit; Silva Junior, Luiz Fernando da
Source: Tetrahedron Letters. Unidade: IQ
Subjects: OXIDAÇÃO, SÍNTESE ORGÂNICA
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ABNT
AHMAD, Anees et al. Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III). Tetrahedron Letters, v. 54, n. 43, p. 5818-5820, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.012. Acesso em: 19 set. 2024.
APA
Ahmad, A., Scarassati, P., Jalalian, N., Olofsson, B., & Silva Junior, L. F. da. (2013). Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III). Tetrahedron Letters, 54( 43), 5818-5820. doi:10.1016/j.tetlet.2013.08.012
NLM
Ahmad A, Scarassati P, Jalalian N, Olofsson B, Silva Junior LF da. Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III) [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5818-5820.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.012
Vancouver
Ahmad A, Scarassati P, Jalalian N, Olofsson B, Silva Junior LF da. Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III) [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5818-5820.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.012
Artigo de periodico
Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ (2013)
Stefani, Hélio Alexandre ; Khan, AMNA N; Manarin, Flávia; Vendramini, Pedro H; Eberlin, Marcos Nogueira
Source: Tetrahedron Letters. Unidade: FCF
Subjects: AMINOÁCIDOS, ITÉRBIO
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´. Tetrahedron Letters, v. 54, n. 46, p. 6204-6207, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.133. Acesso em: 19 set. 2024.
APA
Stefani, H. A., Khan, A. M. N. A. N., Manarin, F., Vendramini, P. H., & Eberlin, M. N. (2013). Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´. Tetrahedron Letters, 54( 46), 6204-6207. doi:10.1016/j.tetlet.2013.08.133
NLM
Stefani HA, Khan AMNAN, Manarin F, Vendramini PH, Eberlin MN. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ [Internet]. Tetrahedron Letters. 2013 ; 54( 46): 6204-6207.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.133
Vancouver
Stefani HA, Khan AMNAN, Manarin F, Vendramini PH, Eberlin MN. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ [Internet]. Tetrahedron Letters. 2013 ; 54( 46): 6204-6207.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.133
Artigo de periodico
Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction (2012)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Manarin, Flávia; Lüdtke, Diogo, Seibert; Zukerman-Schpector, Júlio; Madureira, Lucas Sousa; Tiekink, Edward R. T
Source: Tetrahedron Letters. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, v. 53, n. 14, p. 1742-1747 : + Supplementary materials ( S1-S36), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.01.102. Acesso em: 19 set. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Manarin, F., Lüdtke, D., Zukerman-Schpector, J., Madureira, L. S., & Tiekink, E. R. T. (2012). Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, 53( 14), 1742-1747 : + Supplementary materials ( S1-S36). doi:10.1016/j.tetlet.2012.01.102
NLM
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Vancouver
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Artigo de periodico
Cerium metal-mediated reformatsky-type reaction with ethyl bromosuccinate for the synthesis of novel paraconic acid analogs (2012)
Rodrigues, Shirley M. M.; Nardini, Viviani; Constantino, Maurício Gomes; Silva, Gil Valdo José da
Source: Tetrahedron Letters. Unidades: FCFRP, FFCLRP
Subjects: QUÍMICA ORGÂNICA, CÉRIO
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ABNT
RODRIGUES, Shirley M. M. et al. Cerium metal-mediated reformatsky-type reaction with ethyl bromosuccinate for the synthesis of novel paraconic acid analogs. Tetrahedron Letters, v. 53, p. 6136-6137, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.08.155. Acesso em: 19 set. 2024.
APA
Rodrigues, S. M. M., Nardini, V., Constantino, M. G., & Silva, G. V. J. da. (2012). Cerium metal-mediated reformatsky-type reaction with ethyl bromosuccinate for the synthesis of novel paraconic acid analogs. Tetrahedron Letters, 53, 6136-6137. doi:10.1016/j.tetlet.2012.08.155
NLM
Rodrigues SMM, Nardini V, Constantino MG, Silva GVJ da. Cerium metal-mediated reformatsky-type reaction with ethyl bromosuccinate for the synthesis of novel paraconic acid analogs [Internet]. Tetrahedron Letters. 2012 ; 53 6136-6137.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.08.155
Vancouver
Rodrigues SMM, Nardini V, Constantino MG, Silva GVJ da. Cerium metal-mediated reformatsky-type reaction with ethyl bromosuccinate for the synthesis of novel paraconic acid analogs [Internet]. Tetrahedron Letters. 2012 ; 53 6136-6137.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.08.155
Artigo de periodico
Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for 'Cu POT. 2+' (2012)
García-Beltrán, Olimpo; Mena, Natalia; Friedrich, Leidi Cecilia; Netto-Ferreira, José Carlos; Vargas, Victor; Quina, Frank Herbert ; Núñez, Marco T; Cassels, Bruce K
Source: Tetrahedron Letters. Unidade: IQ
Subjects: FLUORESCÊNCIA, COBRE
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ABNT
GARCÍA-BELTRÁN, Olimpo et al. Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for 'Cu POT. 2+'. Tetrahedron Letters, v. 53, n. 39, p. 5280-5283, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.07.082. Acesso em: 19 set. 2024.
APA
García-Beltrán, O., Mena, N., Friedrich, L. C., Netto-Ferreira, J. C., Vargas, V., Quina, F. H., et al. (2012). Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for 'Cu POT. 2+'. Tetrahedron Letters, 53( 39), 5280-5283. doi:10.1016/j.tetlet.2012.07.082
NLM
García-Beltrán O, Mena N, Friedrich LC, Netto-Ferreira JC, Vargas V, Quina FH, Núñez MT, Cassels BK. Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for 'Cu POT. 2+' [Internet]. Tetrahedron Letters. 2012 ; 53( 39): 5280-5283.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.07.082
Vancouver
García-Beltrán O, Mena N, Friedrich LC, Netto-Ferreira JC, Vargas V, Quina FH, Núñez MT, Cassels BK. Design and synthesis of a new coumarin-based 'turn-on' fluorescent probe selective for 'Cu POT. 2+' [Internet]. Tetrahedron Letters. 2012 ; 53( 39): 5280-5283.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.07.082
Artigo de periodico
Novel cross-coupling reactions between organotellurides and Grignard reagents employing a 'MnCl IND. 2'/CuI catalytic system (2012)
Silva, Márcio Santos da; Ferrarini, Renan dos Santos; Sousa, Bruno Artur de; Toledo, Fabiano Travanca; Comasseto, João Valdir; Gariani, Rogério Aparecido
Source: Tetrahedron Letters. Unidade: IQ
Subjects: COMPOSTOS ORGANOMETÁLICOS, MANGANÊS
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ABNT
SILVA, Márcio Santos da et al. Novel cross-coupling reactions between organotellurides and Grignard reagents employing a 'MnCl IND. 2'/CuI catalytic system. Tetrahedron Letters, v. 53, n. 28, p. 3556-3559, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.04.134. Acesso em: 19 set. 2024.
APA
Silva, M. S. da, Ferrarini, R. dos S., Sousa, B. A. de, Toledo, F. T., Comasseto, J. V., & Gariani, R. A. (2012). Novel cross-coupling reactions between organotellurides and Grignard reagents employing a 'MnCl IND. 2'/CuI catalytic system. Tetrahedron Letters, 53( 28), 3556-3559. doi:10.1016/j.tetlet.2012.04.134
NLM
Silva MS da, Ferrarini R dos S, Sousa BA de, Toledo FT, Comasseto JV, Gariani RA. Novel cross-coupling reactions between organotellurides and Grignard reagents employing a 'MnCl IND. 2'/CuI catalytic system [Internet]. Tetrahedron Letters. 2012 ; 53( 28): 3556-3559.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.04.134
Vancouver
Silva MS da, Ferrarini R dos S, Sousa BA de, Toledo FT, Comasseto JV, Gariani RA. Novel cross-coupling reactions between organotellurides and Grignard reagents employing a 'MnCl IND. 2'/CuI catalytic system [Internet]. Tetrahedron Letters. 2012 ; 53( 28): 3556-3559.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.04.134
Artigo de periodico
Novel sesquiterpene lactones from Eremanthus seidelii (2012)
Sousa, João Paulo Barreto; Tomaz, José Carlos; Silva, Cecilia C. P.; Ellena, Javier ; Lopes, Norberto Peporine; Lopes, João Luis Callegari
Source: Tetrahedron Letters. Unidades: FCFRP, IFSC
Subjects: QUÍMICA ORGÂNICA, PLANTAS, COMPOSTOS CÍCLICOS
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ABNT
SOUSA, João Paulo Barreto et al. Novel sesquiterpene lactones from Eremanthus seidelii. Tetrahedron Letters, v. No 2012, n. 47, p. 6339-6342, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.09.007. Acesso em: 19 set. 2024.
APA
Sousa, J. P. B., Tomaz, J. C., Silva, C. C. P., Ellena, J., Lopes, N. P., & Lopes, J. L. C. (2012). Novel sesquiterpene lactones from Eremanthus seidelii. Tetrahedron Letters, No 2012( 47), 6339-6342. doi:10.1016/j.tetlet.2012.09.007
NLM
Sousa JPB, Tomaz JC, Silva CCP, Ellena J, Lopes NP, Lopes JLC. Novel sesquiterpene lactones from Eremanthus seidelii [Internet]. Tetrahedron Letters. 2012 ; No 2012( 47): 6339-6342.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.09.007
Vancouver
Sousa JPB, Tomaz JC, Silva CCP, Ellena J, Lopes NP, Lopes JLC. Novel sesquiterpene lactones from Eremanthus seidelii [Internet]. Tetrahedron Letters. 2012 ; No 2012( 47): 6339-6342.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.09.007
Artigo de periodico
Practical synthesis of a functionalized 1-oxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (2012)
Quintiliano, Samir Augusto Pino; Silva Junior, Luiz Fernando da
Source: Tetrahedron Letters. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
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ABNT
QUINTILIANO, Samir Augusto Pino e SILVA JUNIOR, Luiz Fernando da. Practical synthesis of a functionalized 1-oxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid. Tetrahedron Letters, v. 53, n. 29, p. 3808-3810 : + Supplementary materials ( S1-S34), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.05.060. Acesso em: 19 set. 2024.
APA
Quintiliano, S. A. P., & Silva Junior, L. F. da. (2012). Practical synthesis of a functionalized 1-oxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid. Tetrahedron Letters, 53( 29), 3808-3810 : + Supplementary materials ( S1-S34). doi:10.1016/j.tetlet.2012.05.060
NLM
Quintiliano SAP, Silva Junior LF da. Practical synthesis of a functionalized 1-oxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid [Internet]. Tetrahedron Letters. 2012 ; 53( 29): 3808-3810 : + Supplementary materials ( S1-S34).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.05.060
Vancouver
Quintiliano SAP, Silva Junior LF da. Practical synthesis of a functionalized 1-oxo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid [Internet]. Tetrahedron Letters. 2012 ; 53( 29): 3808-3810 : + Supplementary materials ( S1-S34).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.05.060
Artigo de periodico
Total synthesis of (-)-indolizidine 167B via an unusual wolff rearrangement from a 'alfa','beta'-unsaturated diazoketone (2012)
Pinho, Vagner D; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron Letters. Unidade: IQSC
Subjects: SÍNTESE QUÍMICA, QUÍMICA ORGÂNICA
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ABNT
PINHO, Vagner D e BURTOLOSO, Antonio Carlos Bender. Total synthesis of (-)-indolizidine 167B via an unusual wolff rearrangement from a 'alfa','beta'-unsaturated diazoketone. Tetrahedron Letters, v. 53, n. 7, p. 876-878, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.12.029. Acesso em: 19 set. 2024.
APA
Pinho, V. D., & Burtoloso, A. C. B. (2012). Total synthesis of (-)-indolizidine 167B via an unusual wolff rearrangement from a 'alfa','beta'-unsaturated diazoketone. Tetrahedron Letters, 53( 7), 876-878. doi:10.1016/j.tetlet.2011.12.029
NLM
Pinho VD, Burtoloso ACB. Total synthesis of (-)-indolizidine 167B via an unusual wolff rearrangement from a 'alfa','beta'-unsaturated diazoketone [Internet]. Tetrahedron Letters. 2012 ; 53( 7): 876-878.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.12.029
Vancouver
Pinho VD, Burtoloso ACB. Total synthesis of (-)-indolizidine 167B via an unusual wolff rearrangement from a 'alfa','beta'-unsaturated diazoketone [Internet]. Tetrahedron Letters. 2012 ; 53( 7): 876-878.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.12.029
Artigo de periodico
Further monoterpene chromane esters from Peperomia obtusifolia: VCD determination of the absolute configuration of a new diastereomeric mixture (2012)
Batista Junior, João Marcos; Batista, Andrea N. L; Kato, Massuo Jorge ; Bolzani, Vanderlan da Silva; López, Silvia Noelí; Nafie, Laurence A; Furlan, Maysa
Source: Tetrahedron Letters. Unidade: IQ
Subjects: PRODUTOS NATURAIS, CROMATOGRAFIA
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ABNT
BATISTA JUNIOR, João Marcos et al. Further monoterpene chromane esters from Peperomia obtusifolia: VCD determination of the absolute configuration of a new diastereomeric mixture. Tetrahedron Letters, v. 53, n. 45, p. 6051-6054, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.08.113. Acesso em: 19 set. 2024.
APA
Batista Junior, J. M., Batista, A. N. L., Kato, M. J., Bolzani, V. da S., López, S. N., Nafie, L. A., & Furlan, M. (2012). Further monoterpene chromane esters from Peperomia obtusifolia: VCD determination of the absolute configuration of a new diastereomeric mixture. Tetrahedron Letters, 53( 45), 6051-6054. doi:10.1016/j.tetlet.2012.08.113
NLM
Batista Junior JM, Batista ANL, Kato MJ, Bolzani V da S, López SN, Nafie LA, Furlan M. Further monoterpene chromane esters from Peperomia obtusifolia: VCD determination of the absolute configuration of a new diastereomeric mixture [Internet]. Tetrahedron Letters. 2012 ; 53( 45): 6051-6054.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.08.113
Vancouver
Batista Junior JM, Batista ANL, Kato MJ, Bolzani V da S, López SN, Nafie LA, Furlan M. Further monoterpene chromane esters from Peperomia obtusifolia: VCD determination of the absolute configuration of a new diastereomeric mixture [Internet]. Tetrahedron Letters. 2012 ; 53( 45): 6051-6054.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2012.08.113
Artigo de periodico
Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles (2011)
Stefani, Hélio Alexandre ; Vieira, Adriano Siqueira; Amaral, Monica Franco Zanini Junqueira; Cooper, Leora
Source: Tetrahedron Letters. Unidade: FCF
Subjects: POTÁSSIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, v. 52, n. 33, p. 4256-4261 + Supplementary Materials ( S1-S7), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.04.072. Acesso em: 19 set. 2024.
APA
Stefani, H. A., Vieira, A. S., Amaral, M. F. Z. J., & Cooper, L. (2011). Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, 52( 33), 4256-4261 + Supplementary Materials ( S1-S7). doi:10.1016/j.tetlet.2011.04.072
NLM
Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
Vancouver
Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
Artigo de periodico
Enzymatic kinetic resolution of organochalcogenides in supercritical 'CO IND. 2' (2011)
Gariani, Rogério Aparecido; Luengo, Fernando Alves Gomes; Vale, Luiz Américo da Silva do; Bazito, Reinaldo Camino ; Comasseto, João Valdir
Source: Tetrahedron Letters. Unidade: IQ
Subjects: CALCOGÊNIOS, DIÓXIDO DE CARBONO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARIANI, Rogério Aparecido et al. Enzymatic kinetic resolution of organochalcogenides in supercritical 'CO IND. 2'. Tetrahedron Letters, v. 52, n. 26, p. 3336-3338, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.04.073. Acesso em: 19 set. 2024.
APA
Gariani, R. A., Luengo, F. A. G., Vale, L. A. da S. do, Bazito, R. C., & Comasseto, J. V. (2011). Enzymatic kinetic resolution of organochalcogenides in supercritical 'CO IND. 2'. Tetrahedron Letters, 52( 26), 3336-3338. doi:10.1016/j.tetlet.2011.04.073
NLM
Gariani RA, Luengo FAG, Vale LA da S do, Bazito RC, Comasseto JV. Enzymatic kinetic resolution of organochalcogenides in supercritical 'CO IND. 2' [Internet]. Tetrahedron Letters. 2011 ; 52( 26): 3336-3338.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.073
Vancouver
Gariani RA, Luengo FAG, Vale LA da S do, Bazito RC, Comasseto JV. Enzymatic kinetic resolution of organochalcogenides in supercritical 'CO IND. 2' [Internet]. Tetrahedron Letters. 2011 ; 52( 26): 3336-3338.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.073
Artigo de periodico
Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids (2011)
Stefani, Hélio Alexandre ; Amaral, Monica Franco Zanini Junqueira; Juaristi, Eusebio
Source: Tetrahedron Letters. Unidade: FCF
Subjects: AMINOÁCIDOS, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre e AMARAL, Monica Franco Zanini Junqueira e JUARISTI, Eusebio. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, v. 52, n. 9, p. 1014-1019, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.12.087. Acesso em: 19 set. 2024.
APA
Stefani, H. A., Amaral, M. F. Z. J., & Juaristi, E. (2011). Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, 52( 9), 1014-1019. doi:10.1016/j.tetlet.2010.12.087
NLM
Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
Vancouver
Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
Artigo de periodico
Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions (2011)
Stefani, Hélio Alexandre ; Amaral, Mônica Franco Zannini Junqueira; Manarin, Flávia; Ando, Rômulo Augusto ; Silva, Nathalia Cristina S; Juaristi, Eusebio
Source: Tetrahedron Letters. Unidades: FCF, IQ
Subjects: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, v. 52, n. 51, p. 6883-6886 : + Supplementary materials ( S1-S6), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.10.011. Acesso em: 19 set. 2024.
APA
Stefani, H. A., Amaral, M. F. Z. J., Manarin, F., Ando, R. A., Silva, N. C. S., & Juaristi, E. (2011). Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, 52( 51), 6883-6886 : + Supplementary materials ( S1-S6). doi:10.1016/j.tetlet.2011.10.011
NLM
Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
Vancouver
Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
Artigo de periodico
A novel labdane diterpene from Acritopappus longifolius (2011)
Ferreira, Fernanda Peres; Marturano, Eduardo Henck; Carollo, Carlos Alexandre; Oliveira, Dionéia Camilo Rodrigues de
Source: Tetrahedron Letters. Unidade: FCFRP
Subjects: COMPOSITAE, QUÍMICA ORGÂNICA, ESPECTROSCOPIA DE MASSA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Fernanda Peres et al. A novel labdane diterpene from Acritopappus longifolius. Tetrahedron Letters, v. 52, n. 2, p. 297-299, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.11.040. Acesso em: 19 set. 2024.
APA
Ferreira, F. P., Marturano, E. H., Carollo, C. A., & Oliveira, D. C. R. de. (2011). A novel labdane diterpene from Acritopappus longifolius. Tetrahedron Letters, 52( 2), 297-299. doi:10.1016/j.tetlet.2010.11.040
NLM
Ferreira FP, Marturano EH, Carollo CA, Oliveira DCR de. A novel labdane diterpene from Acritopappus longifolius [Internet]. Tetrahedron Letters. 2011 ; 52( 2): 297-299.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2010.11.040
Vancouver
Ferreira FP, Marturano EH, Carollo CA, Oliveira DCR de. A novel labdane diterpene from Acritopappus longifolius [Internet]. Tetrahedron Letters. 2011 ; 52( 2): 297-299.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2010.11.040
Artigo de periodico
Tandem reduction + cyclization of ortho-substituted cinnamic esters (2011)
Sass, Daiane Cristina; Lucca Júnior, Emílio Carlos de; Barbosa, Jader da Silva; Oliveira, Kleber Thiago de; Constantino, Maurício Gomes
Source: Tetrahedron Letters. Unidade: FFCLRP
Assunto: QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SASS, Daiane Cristina et al. Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, v. 52, n. 41, p. 5371-5374, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.08.039. Acesso em: 19 set. 2024.
APA
Sass, D. C., Lucca Júnior, E. C. de, Barbosa, J. da S., Oliveira, K. T. de, & Constantino, M. G. (2011). Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, 52( 41), 5371-5374. doi:10.1016/j.tetlet.2011.08.039
NLM
Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
Vancouver
Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 set. 19 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039

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