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  • Source: Synlett. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, PALÁDIO

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    • ABNT

      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: 19 abr. 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 abr. 19 ] 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 abr. 19 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
  • Source: Synlett. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, PALÁDIO

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    • 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: 19 abr. 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 abr. 19 ] 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 abr. 19 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-2008-1078507.pdf
  • Source: Synlett. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, PRODUTOS NATURAIS

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    • ABNT

      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: 19 abr. 2024.
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      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 abr. 19 ] 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 abr. 19 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1088219.pdf
  • Source: Synlett. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      FERRAZ, Helena Maria Carvalho e SANO, Myrian Kazumi e SCALFO, A C. Tellurium and iodine promoted cyclofunctionalization of alkenyl substituted `beta´-keto esters. Synlett, n. 5, p. 567-568, 1999Tradução . . Acesso em: 19 abr. 2024.
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      Ferraz, H. M. C., Sano, M. K., & Scalfo, A. C. (1999). Tellurium and iodine promoted cyclofunctionalization of alkenyl substituted `beta´-keto esters. Synlett, ( 5), 567-568.
    • NLM

      Ferraz HMC, Sano MK, Scalfo AC. Tellurium and iodine promoted cyclofunctionalization of alkenyl substituted `beta´-keto esters. Synlett. 1999 ;( 5): 567-568.[citado 2024 abr. 19 ]
    • Vancouver

      Ferraz HMC, Sano MK, Scalfo AC. Tellurium and iodine promoted cyclofunctionalization of alkenyl substituted `beta´-keto esters. Synlett. 1999 ;( 5): 567-568.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      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: 19 abr. 2024.
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      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 abr. 19 ]
    • 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 abr. 19 ]
  • Source: Synlett. Unidade: FCF

    Subjects: QUÍMICA ORGÂNICA, BIOQUÍMICA, SÍNTESE ORGÂNICA, PALÁDIO, CATÁLISE, TELÚRIO

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    • ABNT

      ZENI, Gilson et al. Synthesis of cross-conjugated geminal enediynes via palladium catalyzed cross-coupling reaction of ketene butyltelluroacetals. Synlett, n. 6, p. 975-977, 2002Tradução . . Acesso em: 19 abr. 2024.
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      Zeni, G., Perin, G., Cella, R., Jacob, R. G., Braga, A. L., Silveira, C. C., & Stefani, H. A. (2002). Synthesis of cross-conjugated geminal enediynes via palladium catalyzed cross-coupling reaction of ketene butyltelluroacetals. Synlett, ( 6), 975-977.
    • NLM

      Zeni G, Perin G, Cella R, Jacob RG, Braga AL, Silveira CC, Stefani HA. Synthesis of cross-conjugated geminal enediynes via palladium catalyzed cross-coupling reaction of ketene butyltelluroacetals. Synlett. 2002 ;( 6): 975-977.[citado 2024 abr. 19 ]
    • Vancouver

      Zeni G, Perin G, Cella R, Jacob RG, Braga AL, Silveira CC, Stefani HA. Synthesis of cross-conjugated geminal enediynes via palladium catalyzed cross-coupling reaction of ketene butyltelluroacetals. Synlett. 2002 ;( 6): 975-977.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidade: FFCLRP

    Assunto: QUÍMICA

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    • ABNT

      DABDOUB, Miguel Joaquim et al. Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes. Synlett, n. 6, p. 986-990, 2009Tradução . . Disponível em: https://doi.org/10.1055/s-0028-1088196. Acesso em: 19 abr. 2024.
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      Dabdoub, M. J., Dabdoub, V. B., Lenardão, É. J., Hurtado, G. R., Barbosa, S. L., Guerrero Júnior, P. G., et al. (2009). Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes. Synlett, ( 6), 986-990. doi:10.1055/s-0028-1088196
    • NLM

      Dabdoub MJ, Dabdoub VB, Lenardão ÉJ, Hurtado GR, Barbosa SL, Guerrero Júnior PG, Nazario CED, Viana LH, Santana AS, Baroni AC de M. Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes [Internet]. Synlett. 2009 ;( 6): 986-990.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1055/s-0028-1088196
    • Vancouver

      Dabdoub MJ, Dabdoub VB, Lenardão ÉJ, Hurtado GR, Barbosa SL, Guerrero Júnior PG, Nazario CED, Viana LH, Santana AS, Baroni AC de M. Synthesis of (Z)-1-organylthiobut-1-en-3-ynes: hydrothiolation of symmetrical and unsymmetrical buta-1,3-diynes [Internet]. Synlett. 2009 ;( 6): 986-990.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1055/s-0028-1088196
  • Source: Synlett. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      ARAUJO, M A e COMASSETO, João Valdir. Stereoselective and convergent route to z- enynes and z-trisubstituted enediynes. Synlett, n. 11, p. 1145, 1995Tradução . . Acesso em: 19 abr. 2024.
    • APA

      Araujo, M. A., & Comasseto, J. V. (1995). Stereoselective and convergent route to z- enynes and z-trisubstituted enediynes. Synlett, (11), 1145.
    • NLM

      Araujo MA, Comasseto JV. Stereoselective and convergent route to z- enynes and z-trisubstituted enediynes. Synlett. 1995 ;(11): 1145.[citado 2024 abr. 19 ]
    • Vancouver

      Araujo MA, Comasseto JV. Stereoselective and convergent route to z- enynes and z-trisubstituted enediynes. Synlett. 1995 ;(11): 1145.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidade: IQSC

    Assunto: FOTOQUÍMICA ORGÂNICA

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    • ABNT

      TALERO, Alexánder G. e BURTOLOSO, Antonio Carlos Bender. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones. Synlett, v. 28, n. 14, p. 1748-1752, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1590977. Acesso em: 19 abr. 2024.
    • APA

      Talero, A. G., & Burtoloso, A. C. B. (2017). Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones. Synlett, 28( 14), 1748-1752. doi:10.1055/s-0036-1590977
    • NLM

      Talero AG, Burtoloso ACB. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones [Internet]. Synlett. 2017 ; 28( 14): 1748-1752.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1055/s-0036-1590977
    • Vancouver

      Talero AG, Burtoloso ACB. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones [Internet]. Synlett. 2017 ; 28( 14): 1748-1752.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1055/s-0036-1590977
  • Source: Synlett. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      CHIEFFI, A. e COMASSETO, João Valdir e SNIECKUS, V. Selective generation of mono- and 1,1´-dilithioferrocenes by lithium-tellurium exchange. Efficient routes to mono- and symmetrical and unsymmetrical 1,1´-di-substituted ferrocenes. Synlett, n. 2, p. 269-271, 2000Tradução . . Acesso em: 19 abr. 2024.
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      Chieffi, A., Comasseto, J. V., & Snieckus, V. (2000). Selective generation of mono- and 1,1´-dilithioferrocenes by lithium-tellurium exchange. Efficient routes to mono- and symmetrical and unsymmetrical 1,1´-di-substituted ferrocenes. Synlett, ( 2), 269-271.
    • NLM

      Chieffi A, Comasseto JV, Snieckus V. Selective generation of mono- and 1,1´-dilithioferrocenes by lithium-tellurium exchange. Efficient routes to mono- and symmetrical and unsymmetrical 1,1´-di-substituted ferrocenes. Synlett. 2000 ;( 2): 269-271.[citado 2024 abr. 19 ]
    • Vancouver

      Chieffi A, Comasseto JV, Snieckus V. Selective generation of mono- and 1,1´-dilithioferrocenes by lithium-tellurium exchange. Efficient routes to mono- and symmetrical and unsymmetrical 1,1´-di-substituted ferrocenes. Synlett. 2000 ;( 2): 269-271.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      SILVEIRA, C C et al. Preparation of vinyl tellurides via a simplified ylidation reaction. Synlett, n. 1 , p. 58-60, 1995Tradução . . Acesso em: 19 abr. 2024.
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      Silveira, C. C., Perin, G., Braga, A. L., & Petragnani, N. (1995). Preparation of vinyl tellurides via a simplified ylidation reaction. Synlett, (1 ), 58-60.
    • NLM

      Silveira CC, Perin G, Braga AL, Petragnani N. Preparation of vinyl tellurides via a simplified ylidation reaction. Synlett. 1995 ;(1 ): 58-60.[citado 2024 abr. 19 ]
    • Vancouver

      Silveira CC, Perin G, Braga AL, Petragnani N. Preparation of vinyl tellurides via a simplified ylidation reaction. Synlett. 1995 ;(1 ): 58-60.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidade: FFCLRP

    Assunto: QUÍMICA INORGÂNICA

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    • ABNT

      DABDOUB, Miguel Joaquim e ROTTA, J C G. Homopropargylic alchohols from propargylic derivatives via butyltelluro allene componds. Synlett, v. 6 , p. 526-8, 1996Tradução . . Acesso em: 19 abr. 2024.
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      Dabdoub, M. J., & Rotta, J. C. G. (1996). Homopropargylic alchohols from propargylic derivatives via butyltelluro allene componds. Synlett, 6 , 526-8.
    • NLM

      Dabdoub MJ, Rotta JCG. Homopropargylic alchohols from propargylic derivatives via butyltelluro allene componds. Synlett. 1996 ;6 526-8.[citado 2024 abr. 19 ]
    • Vancouver

      Dabdoub MJ, Rotta JCG. Homopropargylic alchohols from propargylic derivatives via butyltelluro allene componds. Synlett. 1996 ;6 526-8.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      MARINO, J P e TUCCI, F C e COMASSETO, João Valdir. Efficient preparation of functionalized z-vinylcuprates from terminal acetylenes and their reactions with epoxides. Synlett, n. 10, p. 761-3, 1993Tradução . . Acesso em: 19 abr. 2024.
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      Marino, J. P., Tucci, F. C., & Comasseto, J. V. (1993). Efficient preparation of functionalized z-vinylcuprates from terminal acetylenes and their reactions with epoxides. Synlett, (10), 761-3.
    • NLM

      Marino JP, Tucci FC, Comasseto JV. Efficient preparation of functionalized z-vinylcuprates from terminal acetylenes and their reactions with epoxides. Synlett. 1993 ;(10): 761-3.[citado 2024 abr. 19 ]
    • Vancouver

      Marino JP, Tucci FC, Comasseto JV. Efficient preparation of functionalized z-vinylcuprates from terminal acetylenes and their reactions with epoxides. Synlett. 1993 ;(10): 761-3.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidades: FFCLRP, FCFRP

    Subjects: NITRILAS, BORRACHA, COMPOSTOS ORGANOMETÁLICOS, COMPOSTOS AROMÁTICOS

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      SANTOS, Fernanda M. dos et al. Directed functionalization of cyano-substituted furans and thiophenes with TMPMgCl•LiCl. Synlett, v. 26, n. 20, p. 2795-2800, 2015Tradução . . Disponível em: https://doi.org/10.1055/s-0035-1560586. Acesso em: 19 abr. 2024.
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      Santos, F. M. dos, Batista, J. H. C., Vessecchi, R., & Clososki, G. C. (2015). Directed functionalization of cyano-substituted furans and thiophenes with TMPMgCl•LiCl. Synlett, 26( 20), 2795-2800. doi:10.1055/s-0035-1560586
    • NLM

      Santos FM dos, Batista JHC, Vessecchi R, Clososki GC. Directed functionalization of cyano-substituted furans and thiophenes with TMPMgCl•LiCl [Internet]. Synlett. 2015 ; 26( 20): 2795-2800.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1055/s-0035-1560586
    • Vancouver

      Santos FM dos, Batista JHC, Vessecchi R, Clososki GC. Directed functionalization of cyano-substituted furans and thiophenes with TMPMgCl•LiCl [Internet]. Synlett. 2015 ; 26( 20): 2795-2800.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1055/s-0035-1560586
  • Source: Synlett. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      CHIEFFI, A e COMASSETO, João Valdir. Coupling reaction between vinylic tellurides and lower order cyanocuprates. Synlett, n. 6 , p. 671-4, 1995Tradução . . Acesso em: 19 abr. 2024.
    • APA

      Chieffi, A., & Comasseto, J. V. (1995). Coupling reaction between vinylic tellurides and lower order cyanocuprates. Synlett, (6 ), 671-4.
    • NLM

      Chieffi A, Comasseto JV. Coupling reaction between vinylic tellurides and lower order cyanocuprates. Synlett. 1995 ;(6 ): 671-4.[citado 2024 abr. 19 ]
    • Vancouver

      Chieffi A, Comasseto JV. Coupling reaction between vinylic tellurides and lower order cyanocuprates. Synlett. 1995 ;(6 ): 671-4.[citado 2024 abr. 19 ]
  • Source: Synlett. Unidade: IQSC

    Subjects: PRODUTOS NATURAIS, QUÍMICA

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      BURTOLOSO, Antonio Carlos Bender. Catalytic enantioselective 'beta'-arylation of carbonyl compounds. Synlett, n. 2, p. 320-327, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf. Acesso em: 19 abr. 2024.
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      Burtoloso, A. C. B. (2009). Catalytic enantioselective 'beta'-arylation of carbonyl compounds. Synlett, ( 2), 320-327. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
    • NLM

      Burtoloso ACB. Catalytic enantioselective 'beta'-arylation of carbonyl compounds [Internet]. Synlett. 2009 ;( 2): 320-327.[citado 2024 abr. 19 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
    • Vancouver

      Burtoloso ACB. Catalytic enantioselective 'beta'-arylation of carbonyl compounds [Internet]. Synlett. 2009 ;( 2): 320-327.[citado 2024 abr. 19 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
  • Source: Synlett. Unidade: IQ

    Subjects: TÁLIO, SÍNTESE ORGÂNICA

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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: 19 abr. 2024.
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      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 abr. 19 ] 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 abr. 19 ] Available from: https://doi.org/10.1055/s-0033-1340472
  • Source: Synlett. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, TÁLIO

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      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: 19 abr. 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 abr. 19 ] 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 abr. 19 ] Available from: https://doi.org/10.1055/s-0033-1340472
  • Source: Synlett. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, BIOQUÍMICA ORGÂNICA

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      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: 19 abr. 2024.
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      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 abr. 19 ]
    • 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 abr. 19 ]
  • Source: Synlett. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      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: 19 abr. 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 abr. 19 ]
    • 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 abr. 19 ]

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