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ABNT
SILVA JUNIOR, Luiz Fernando da. Accdouvntentures in ring-contraction reactions. Synlett, v. 25, p. 466-476, 2014Tradução . . Disponível em: https://doi.org/10.1055/s-0033-1340472. Acesso em: 02 out. 2024.
APA
Silva Junior, L. F. da. (2014). Accdouvntentures in ring-contraction reactions. Synlett, 25, 466-476. doi:10.1055/s-0033-1340472
NLM
Silva Junior LF da. Accdouvntentures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25 466-476.[citado 2024 out. 02 ] Available from: https://doi.org/10.1055/s-0033-1340472
Vancouver
Silva Junior LF da. Accdouvntentures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25 466-476.[citado 2024 out. 02 ] Available from: https://doi.org/10.1055/s-0033-1340472
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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SILVA JUNIOR, Luiz Fernando da. Adventures in ring-contraction reactions. Synlett, v. 25, n. 4, p. 466-476, 2014Tradução . . Disponível em: https://doi.org/10.1055/s-0033-1340472. Acesso em: 02 out. 2024.
APA
Silva Junior, L. F. da. (2014). Adventures in ring-contraction reactions. Synlett, 25( 4), 466-476. doi:10.1055/s-0033-1340472
NLM
Silva Junior LF da. Adventures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25( 4): 466-476.[citado 2024 out. 02 ] Available from: https://doi.org/10.1055/s-0033-1340472
Vancouver
Silva Junior LF da. Adventures in ring-contraction reactions [Internet]. Synlett. 2014 ; 25( 4): 466-476.[citado 2024 out. 02 ] Available from: https://doi.org/10.1055/s-0033-1340472
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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MOURA, Sidnei e PINTO, Ernani. Synthesis of cyclic guanidine intermediates of anatoxin-a(s) in both racemic and enantiomerically pure forms. Synlett, n. 6, p. 967-969, 2010Tradução . . Acesso em: 02 out. 2024.
APA
Moura, S., & Pinto, E. (2010). Synthesis of cyclic guanidine intermediates of anatoxin-a(s) in both racemic and enantiomerically pure forms. Synlett, ( 6), 967-969.
NLM
Moura S, Pinto E. Synthesis of cyclic guanidine intermediates of anatoxin-a(s) in both racemic and enantiomerically pure forms. Synlett. 2010 ;( 6): 967-969.[citado 2024 out. 02 ]
Vancouver
Moura S, Pinto E. Synthesis of cyclic guanidine intermediates of anatoxin-a(s) in both racemic and enantiomerically pure forms. Synlett. 2010 ;( 6): 967-969.[citado 2024 out. 02 ]
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GUEOGJIAN, Kemilla et al. 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett, n. 3, p. 427-432, 2010Tradução . . Acesso em: 02 out. 2024.
APA
Gueogjian, K., Singh, F. V., Pena, J. M., Amaral, M. F. Z. J., & Stefani, H. A. (2010). 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett, ( 3), 427-432.
NLM
Gueogjian K, Singh FV, Pena JM, Amaral MFZJ, Stefani HA. 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett. 2010 ;( 3): 427-432.[citado 2024 out. 02 ]
Vancouver
Gueogjian K, Singh FV, Pena JM, Amaral MFZJ, Stefani HA. 'Alpha'-Arylation and alkynylation of cyclic 'alpha'-iodoenones using palladium-catalyzed cross-coupling reactions with trifluoroborate salts. Synlett. 2010 ;( 3): 427-432.[citado 2024 out. 02 ]
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WENDLER, Edison P. e SANTOS, Alcindo Aparecido dos. The use of butyl organotellurides in the synthesis of natural bioactive compounds. Synlett, n. 7, p. 1034-1040, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1088219.pdf. Acesso em: 02 out. 2024.
APA
Wendler, E. P., & Santos, A. A. dos. (2009). The use of butyl organotellurides in the synthesis of natural bioactive compounds. Synlett, ( 7), 1034-1040. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1088219.pdf
NLM
Wendler EP, Santos AA dos. The use of butyl organotellurides in the synthesis of natural bioactive compounds [Internet]. Synlett. 2009 ;( 7): 1034-1040.[citado 2024 out. 02 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1088219.pdf
Vancouver
Wendler EP, Santos AA dos. The use of butyl organotellurides in the synthesis of natural bioactive compounds [Internet]. Synlett. 2009 ;( 7): 1034-1040.[citado 2024 out. 02 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1088219.pdf
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SINGH, Fateh Veer e STEFANI, Hélio Alexandre. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides. Synlett, n. 20, p. 3221-3225, 2008Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf. Acesso em: 02 out. 2024.
APA
Singh, F. V., & Stefani, H. A. (2008). Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides. Synlett, ( 20), 3221-3225. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
NLM
Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides [Internet]. Synlett. 2008 ;( 20): 3221-3225.[citado 2024 out. 02 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
Vancouver
Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides [Internet]. Synlett. 2008 ;( 20): 3221-3225.[citado 2024 out. 02 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SINGH, Fateh Veer et al. Ultrasound-assisted synthesis of functionalized 1,3-enynes by palladium- catalyzed cross-coupling reaction of 'alfa'-styrylbutyltelluride with alkynyltrifluoroborate salts. Synlett, n. 12, p. 1889-1893, 2008Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-2008-1078507.pdf. Acesso em: 02 out. 2024.
APA
Singh, F. V., Weber, M., Guadagnin, R. C., & Stefani, H. A. (2008). Ultrasound-assisted synthesis of functionalized 1,3-enynes by palladium- catalyzed cross-coupling reaction of 'alfa'-styrylbutyltelluride with alkynyltrifluoroborate salts. Synlett, ( 12), 1889-1893. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-2008-1078507.pdf
NLM
Singh FV, Weber M, Guadagnin RC, Stefani HA. Ultrasound-assisted synthesis of functionalized 1,3-enynes by palladium- catalyzed cross-coupling reaction of 'alfa'-styrylbutyltelluride with alkynyltrifluoroborate salts [Internet]. Synlett. 2008 ;( 12): 1889-1893.[citado 2024 out. 02 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-2008-1078507.pdf
Vancouver
Singh FV, Weber M, Guadagnin RC, Stefani HA. Ultrasound-assisted synthesis of functionalized 1,3-enynes by palladium- catalyzed cross-coupling reaction of 'alfa'-styrylbutyltelluride with alkynyltrifluoroborate salts [Internet]. Synlett. 2008 ;( 12): 1889-1893.[citado 2024 out. 02 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-2008-1078507.pdf
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ABNT
NIHEI, Ken-ichi et al. 2-nitro- and 2,4-dinitrobenzenesulfonamides as protecting groups for primary amines. Synlett, n. 7, p. 1167-1169, 2001Tradução . . Acesso em: 02 out. 2024.
APA
Nihei, K. -ichi, Kato, M. J., Yamane, T., Palma, M. S., & Konno, K. (2001). 2-nitro- and 2,4-dinitrobenzenesulfonamides as protecting groups for primary amines. Synlett, ( 7), 1167-1169.
NLM
Nihei K-ichi, Kato MJ, Yamane T, Palma MS, Konno K. 2-nitro- and 2,4-dinitrobenzenesulfonamides as protecting groups for primary amines. Synlett. 2001 ;( 7): 1167-1169.[citado 2024 out. 02 ]
Vancouver
Nihei K-ichi, Kato MJ, Yamane T, Palma MS, Konno K. 2-nitro- and 2,4-dinitrobenzenesulfonamides as protecting groups for primary amines. Synlett. 2001 ;( 7): 1167-1169.[citado 2024 out. 02 ]
