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  • Source: Synthetic Communications. Unidade: IQ

    Subjects: ULTRASSOM, SÍNTESE QUÍMICA

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      FRANCO, Maria Silvana Freire et al. Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones. Synthetic Communications, v. 45, n. 6, p. 692-701, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2014.978504. Acesso em: 24 abr. 2024.
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      Franco, M. S. F., Casagrande, G. A., Raminelli, C., Moura, S., Rossatto, M., Quina, F. H., et al. (2015). Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones. Synthetic Communications, 45( 6), 692-701. doi:10.1080/00397911.2014.978504
    • NLM

      Franco MSF, Casagrande GA, Raminelli C, Moura S, Rossatto M, Quina FH, Pereira CMP de, Flores AFC, Pizzuti L. Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones [Internet]. Synthetic Communications. 2015 ; 45( 6): 692-701.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2014.978504
    • Vancouver

      Franco MSF, Casagrande GA, Raminelli C, Moura S, Rossatto M, Quina FH, Pereira CMP de, Flores AFC, Pizzuti L. Ultrasound-promoted environmentally friendly synthesis of 5-(3,3,3-trifluoro-2-oxopropylidene)pyrrolidin-2-ones [Internet]. Synthetic Communications. 2015 ; 45( 6): 692-701.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2014.978504
  • Source: Synthetic Communications. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      COMASSETO, João Valdir e BERRIEL, J. Transmetallation between vinylic tellurides and higher order cyanoenprotes: in situ formation of vinyl cuprates. Synthetic Communications, v. 20, p. 1681-5, 1990Tradução . . Acesso em: 24 abr. 2024.
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      Comasseto, J. V., & Berriel, J. (1990). Transmetallation between vinylic tellurides and higher order cyanoenprotes: in situ formation of vinyl cuprates. Synthetic Communications, 20, 1681-5.
    • NLM

      Comasseto JV, Berriel J. Transmetallation between vinylic tellurides and higher order cyanoenprotes: in situ formation of vinyl cuprates. Synthetic Communications. 1990 ;20 1681-5.[citado 2024 abr. 24 ]
    • Vancouver

      Comasseto JV, Berriel J. Transmetallation between vinylic tellurides and higher order cyanoenprotes: in situ formation of vinyl cuprates. Synthetic Communications. 1990 ;20 1681-5.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAGENTES ORGÂNICOS

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      FERRAZ, H M C e RIBEIRO, C M R. Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications, v. 22, n. 3 , p. 399-404, 1992Tradução . . Acesso em: 24 abr. 2024.
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      Ferraz, H. M. C., & Ribeiro, C. M. R. (1992). Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications, 22( 3 ), 399-404.
    • NLM

      Ferraz HMC, Ribeiro CMR. Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications. 1992 ;22( 3 ): 399-404.[citado 2024 abr. 24 ]
    • Vancouver

      Ferraz HMC, Ribeiro CMR. Thallium (iii) salts -induced lactonizations of unsaturated carboxilic acids. Synthetic Communications. 1992 ;22( 3 ): 399-404.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidades: FFCLRP, IQ

    Assunto: QUÍMICA ORGÂNICA

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      CONSTANTINO, Maurício Gomes et al. Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone. Synthetic Communications, v. 31, n. 21, p. 3329-3336, 2001Tradução . . Disponível em: http://www.dekker.com/catalog/results.jsp?action=getSearchForm. Acesso em: 24 abr. 2024.
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      Constantino, M. G., Beatriz, A., Silva, G. V. J. da, & Zukerman-Schpector, J. (2001). Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone. Synthetic Communications, 31( 21), 3329-3336. Recuperado de http://www.dekker.com/catalog/results.jsp?action=getSearchForm
    • NLM

      Constantino MG, Beatriz A, Silva GVJ da, Zukerman-Schpector J. Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone [Internet]. Synthetic Communications. 2001 ; 31( 21): 3329-3336.[citado 2024 abr. 24 ] Available from: http://www.dekker.com/catalog/results.jsp?action=getSearchForm
    • Vancouver

      Constantino MG, Beatriz A, Silva GVJ da, Zukerman-Schpector J. Synthetic studies on the diels-alder adduct from 3,4-dimethoxyfuran and benzoquinone [Internet]. Synthetic Communications. 2001 ; 31( 21): 3329-3336.[citado 2024 abr. 24 ] Available from: http://www.dekker.com/catalog/results.jsp?action=getSearchForm
  • Source: Synthetic Communications. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      DONATE, Paulo Marcos et al. Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications, v. 29, n. 17, p. 2923-2936, 1999Tradução . . Acesso em: 24 abr. 2024.
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      Donate, P. M., Constantino, M. G., Silva, R. da, & Pedersoli, S. (1999). Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications, 29( 17), 2923-2936.
    • NLM

      Donate PM, Constantino MG, Silva R da, Pedersoli S. Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications. 1999 ; 29( 17): 2923-2936.[citado 2024 abr. 24 ]
    • Vancouver

      Donate PM, Constantino MG, Silva R da, Pedersoli S. Synthesis of substituted 'GAMA'- butyrolactones: 'BETA'-hydroxymethyl-, 'BETA'-methylene and cyclopropane derivatives. Synthetic Communications. 1999 ; 29( 17): 2923-2936.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidades: FCFRP, FFCLRP

    Subjects: PEPTÍDEOS, SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      SILVA, Eduardo H. B et al. Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, v. 45, n. 15, p. 1761-1767, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1042591. Acesso em: 24 abr. 2024.
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      Silva, E. H. B., Emery, F. da S., Del Ponte, G., & Donate, P. M. (2015). Synthesis of some functionalized peptomers via UGI four-component reaction. Synthetic Communications, 45( 15), 1761-1767. doi:10.1080/00397911.2015.1042591
    • NLM

      Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
    • Vancouver

      Silva EHB, Emery F da S, Del Ponte G, Donate PM. Synthesis of some functionalized peptomers via UGI four-component reaction [Internet]. Synthetic Communications. 2015 ; 45( 15): 1761-1767.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2015.1042591
  • Source: Synthetic Communications. Unidade: IQSC

    Subjects: QUÍMICA MÉDICA, SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA, REAÇÕES QUÍMICAS

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      BRITTO, Marcelo Moreira et al. Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides. Synthetic Communications, v. 36, n. 22, p. 3359-3369, 2006Tradução . . Disponível em: http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398. Acesso em: 24 abr. 2024.
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      Britto, M. M., Almeida, T. M. G., Leitão, A., Donnici, C. L., Lopes, M. T. P., & Montanari, C. A. (2006). Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides. Synthetic Communications, 36( 22), 3359-3369. Recuperado de http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398
    • NLM

      Britto MM, Almeida TMG, Leitão A, Donnici CL, Lopes MTP, Montanari CA. Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides [Internet]. Synthetic Communications. 2006 ; 36( 22): 3359-3369.[citado 2024 abr. 24 ] Available from: http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398
    • Vancouver

      Britto MM, Almeida TMG, Leitão A, Donnici CL, Lopes MTP, Montanari CA. Synthesis of mesoionic 4-(para-substituted phenyl-5-2,4-dichlorophenyl)-1,3-4-thiadiazolium-2-aminides by direct cyclization via acylation of thiosemicarbazides [Internet]. Synthetic Communications. 2006 ; 36( 22): 3359-3369.[citado 2024 abr. 24 ] Available from: http://www.journalsonline.tandf.co.uk/openurl.asp?genre=article&id=doi:10.1080/00397910600941398
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA (QUÍMICA)

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      FRAGA, R L et al. Synthesis of dibenzocycloactadienes by anodic oxidation. Synthetic Communications, v. 21, p. 1331-6, 1992Tradução . . Acesso em: 24 abr. 2024.
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      Fraga, R. L., Capelato, M. D., Vieira, P. C., Yoshida, M., & Kato, M. J. (1992). Synthesis of dibenzocycloactadienes by anodic oxidation. Synthetic Communications, 21, 1331-6.
    • NLM

      Fraga RL, Capelato MD, Vieira PC, Yoshida M, Kato MJ. Synthesis of dibenzocycloactadienes by anodic oxidation. Synthetic Communications. 1992 ;21 1331-6.[citado 2024 abr. 24 ]
    • Vancouver

      Fraga RL, Capelato MD, Vieira PC, Yoshida M, Kato MJ. Synthesis of dibenzocycloactadienes by anodic oxidation. Synthetic Communications. 1992 ;21 1331-6.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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      FERREIRA, J T B e SIMONELLI, F e COMASSETO, João Valdir. Synthesis of diarylselenides and diarylsulfides under phase transfer conditions. Synthetic Communications, v. 16, n. 11, p. 1335-41, 1986Tradução . . Acesso em: 24 abr. 2024.
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      Ferreira, J. T. B., Simonelli, F., & Comasseto, J. V. (1986). Synthesis of diarylselenides and diarylsulfides under phase transfer conditions. Synthetic Communications, 16( 11), 1335-41.
    • NLM

      Ferreira JTB, Simonelli F, Comasseto JV. Synthesis of diarylselenides and diarylsulfides under phase transfer conditions. Synthetic Communications. 1986 ;16( 11): 1335-41.[citado 2024 abr. 24 ]
    • Vancouver

      Ferreira JTB, Simonelli F, Comasseto JV. Synthesis of diarylselenides and diarylsulfides under phase transfer conditions. Synthetic Communications. 1986 ;16( 11): 1335-41.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: FFCLRP

    Assunto: QUÍMICA

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      DONATE, Paulo Marcos et al. Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications, v. 31, n. 1, p. 141-150, 2001Tradução . . Acesso em: 24 abr. 2024.
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      Donate, P. M., Silva, R. da, Silva, G. V. J. da, & Alemán, C. (2001). Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications, 31( 1), 141-150.
    • NLM

      Donate PM, Silva R da, Silva GVJ da, Alemán C. Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications. 2001 ; 31( 1): 141-150.[citado 2024 abr. 24 ]
    • Vancouver

      Donate PM, Silva R da, Silva GVJ da, Alemán C. Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications. 2001 ; 31( 1): 141-150.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: FFCLRP

    Assunto: QUÍMICA

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      CONSTANTINO, Maurício Gomes et al. Synthesis of an allylic spiro-lactone. Synthetic Communications, v. 22, n. 19, p. 2859-64, 1992Tradução . . Acesso em: 24 abr. 2024.
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      Constantino, M. G., Beltrame Junior, M., Medeiros, E. F., & Silva, G. V. J. (1992). Synthesis of an allylic spiro-lactone. Synthetic Communications, 22( 19), 2859-64.
    • NLM

      Constantino MG, Beltrame Junior M, Medeiros EF, Silva GVJ. Synthesis of an allylic spiro-lactone. Synthetic Communications. 1992 ;22( 19): 2859-64.[citado 2024 abr. 24 ]
    • Vancouver

      Constantino MG, Beltrame Junior M, Medeiros EF, Silva GVJ. Synthesis of an allylic spiro-lactone. Synthetic Communications. 1992 ;22( 19): 2859-64.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: FFCLRP

    Assunto: QUÍMICA

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      NAVARRO, M e DE GIOVANI, Wagner Ferraresi e ROMERO, José Ricardo. Synthesis of aldehydes, ketones and carboryeic acids by selective oxidations of alcohols using a polypyridyl complex of ruthenium (iv). Synthetic Communications, v. 20, n. 3 , p. 399-406, 1990Tradução . . Acesso em: 24 abr. 2024.
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      Navarro, M., De Giovani, W. F., & Romero, J. R. (1990). Synthesis of aldehydes, ketones and carboryeic acids by selective oxidations of alcohols using a polypyridyl complex of ruthenium (iv). Synthetic Communications, 20( 3 ), 399-406.
    • NLM

      Navarro M, De Giovani WF, Romero JR. Synthesis of aldehydes, ketones and carboryeic acids by selective oxidations of alcohols using a polypyridyl complex of ruthenium (iv). Synthetic Communications. 1990 ;20( 3 ): 399-406.[citado 2024 abr. 24 ]
    • Vancouver

      Navarro M, De Giovani WF, Romero JR. Synthesis of aldehydes, ketones and carboryeic acids by selective oxidations of alcohols using a polypyridyl complex of ruthenium (iv). Synthetic Communications. 1990 ;20( 3 ): 399-406.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: FCF

    Subjects: FARMACOLOGIA, COMPOSTOS HETEROCÍCLICOS

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      STEFANI, Hélio Alexandre e AVILA, Elisabete de. Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications, v. 32, n. 13, p. 2041-2047, 2002Tradução . . Acesso em: 24 abr. 2024.
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      Stefani, H. A., & Avila, E. de. (2002). Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications, 32( 13), 2041-2047.
    • NLM

      Stefani HA, Avila E de. Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications. 2002 ; 32( 13): 2041-2047.[citado 2024 abr. 24 ]
    • Vancouver

      Stefani HA, Avila E de. Synthesis of 4,5-dihydropyrroles by cyclofunctionalization from 'beta'-enamino esters. Synthetic Communications. 2002 ; 32( 13): 2041-2047.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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      STEFANI, Hélio Alexandre e COMASSETO, João Valdir e PETRAGNANI, N. Synthesis of 'ALFA' - telluroketones. Synthetic Communications, v. 17, n. 4 , p. 443-50, 1987Tradução . . Acesso em: 24 abr. 2024.
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      Stefani, H. A., Comasseto, J. V., & Petragnani, N. (1987). Synthesis of 'ALFA' - telluroketones. Synthetic Communications, 17( 4 ), 443-50.
    • NLM

      Stefani HA, Comasseto JV, Petragnani N. Synthesis of 'ALFA' - telluroketones. Synthetic Communications. 1987 ;17( 4 ): 443-50.[citado 2024 abr. 24 ]
    • Vancouver

      Stefani HA, Comasseto JV, Petragnani N. Synthesis of 'ALFA' - telluroketones. Synthetic Communications. 1987 ;17( 4 ): 443-50.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: IQSC

    Assunto: FÍSICO-QUÍMICA

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      VASCONCELLOS, Mario L A A et al. Synthesis ans structural determination of new potential chiral tridentate ligands derivated from 1-(R)-(+)-camphor. Synthetic Communications, v. 28, n. 21, p. 4077-4085, 1998Tradução . . Acesso em: 24 abr. 2024.
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      Vasconcellos, M. L. A. A., Mellão, M. L., Barreiros, U. G., Branco, M. C., Gambardella, M. T. do P., Ramos, O. F., & Ribeiro, M. (1998). Synthesis ans structural determination of new potential chiral tridentate ligands derivated from 1-(R)-(+)-camphor. Synthetic Communications, 28( 21), 4077-4085.
    • NLM

      Vasconcellos MLAA, Mellão ML, Barreiros UG, Branco MC, Gambardella MT do P, Ramos OF, Ribeiro M. Synthesis ans structural determination of new potential chiral tridentate ligands derivated from 1-(R)-(+)-camphor. Synthetic Communications. 1998 ;28( 21): 4077-4085.[citado 2024 abr. 24 ]
    • Vancouver

      Vasconcellos MLAA, Mellão ML, Barreiros UG, Branco MC, Gambardella MT do P, Ramos OF, Ribeiro M. Synthesis ans structural determination of new potential chiral tridentate ligands derivated from 1-(R)-(+)-camphor. Synthetic Communications. 1998 ;28( 21): 4077-4085.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidades: FCF, IQ

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA FARMACÊUTICA, FARMACOLOGIA

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      STEFANI, Hélio Alexandre et al. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications, v. 33, n. 12, p. 2161-2166, 2003Tradução . . Acesso em: 24 abr. 2024.
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      Stefani, H. A., Petragnani, N., Ascenso, M. F. C., & Zeni, G. (2003). Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications, 33( 12), 2161-2166.
    • NLM

      Stefani HA, Petragnani N, Ascenso MFC, Zeni G. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications. 2003 ; 33( 12): 2161-2166.[citado 2024 abr. 24 ]
    • Vancouver

      Stefani HA, Petragnani N, Ascenso MFC, Zeni G. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications. 2003 ; 33( 12): 2161-2166.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: REAÇÕES ORGÂNICAS, QUÍMICA ORGÂNICA

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      CAMILO, Fernanda Ferraz e GRUBER, Jonas. Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene. Synthetic Communications, v. 42, n. 3, p. 394-401, 2012Tradução . . Disponível em: https://doi.org/10.1080/00397911.2010.524962. Acesso em: 24 abr. 2024.
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      Camilo, F. F., & Gruber, J. (2012). Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene. Synthetic Communications, 42( 3), 394-401. doi:10.1080/00397911.2010.524962
    • NLM

      Camilo FF, Gruber J. Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene [Internet]. Synthetic Communications. 2012 ; 42( 3): 394-401.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2010.524962
    • Vancouver

      Camilo FF, Gruber J. Stereoselective synthesis of novel Diels-Alder adducts of 'rô'-substituted cyclopentadiene [Internet]. Synthetic Communications. 2012 ; 42( 3): 394-401.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2010.524962
  • Source: Synthetic Communications. Unidades: FFCLRP, IQSC

    Assunto: FÍSICO-QUÍMICA ORGÂNICA

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      CONSTANTINO, Maurício Gomes et al. Stereoselective synthesis of 'BETA'-hydroxy- and 'BETA'-ethoxy-'delta'-lactones: model structures for compounds isolated from Otoba parvifolia. Synthetic Communications, v. 27, n. 24, p. 4285-4295, 1997Tradução . . Acesso em: 24 abr. 2024.
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      Constantino, M. G., Matias, L. G. de O., Silva, G. V. J. da, Heleno, V. C. G., & Gambardella, M. T. do P. (1997). Stereoselective synthesis of 'BETA'-hydroxy- and 'BETA'-ethoxy-'delta'-lactones: model structures for compounds isolated from Otoba parvifolia. Synthetic Communications, 27( 24), 4285-4295.
    • NLM

      Constantino MG, Matias LG de O, Silva GVJ da, Heleno VCG, Gambardella MT do P. Stereoselective synthesis of 'BETA'-hydroxy- and 'BETA'-ethoxy-'delta'-lactones: model structures for compounds isolated from Otoba parvifolia. Synthetic Communications. 1997 ; 27( 24): 4285-4295.[citado 2024 abr. 24 ]
    • Vancouver

      Constantino MG, Matias LG de O, Silva GVJ da, Heleno VCG, Gambardella MT do P. Stereoselective synthesis of 'BETA'-hydroxy- and 'BETA'-ethoxy-'delta'-lactones: model structures for compounds isolated from Otoba parvifolia. Synthetic Communications. 1997 ; 27( 24): 4285-4295.[citado 2024 abr. 24 ]
  • Source: Synthetic Communications. Unidade: FCF

    Subjects: PALÁDIO, COMPOSTOS HETEROCÍCLICOS

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      REIS, Joel Savi dos et al. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, v. 49, n. 10, p. 1252-1261, 2019Tradução . . Disponível em: https://doi.org/10.1080/00397911.2019.1595657. Acesso em: 24 abr. 2024.
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      Reis, J. S. dos, Caracelli, I., Schpector, J. Z., & Stefani, H. A. (2019). Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, 49( 10), 1252-1261. doi:10.1080/00397911.2019.1595657
    • NLM

      Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2019.1595657
    • Vancouver

      Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1080/00397911.2019.1595657
  • Source: Synthetic Communications. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      DONNICI, Claudio Luis et al. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications, v. 40, n. 3, p. 342-350, 2010Tradução . . Acesso em: 24 abr. 2024.
    • APA

      Donnici, C. L., Pereira, E. H. T., Lopes, J. C. D., Marzorati, L., & Wladislaw, B. (2010). Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications, 40( 3), 342-350.
    • NLM

      Donnici CL, Pereira EHT, Lopes JCD, Marzorati L, Wladislaw B. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications. 2010 ; 40( 3): 342-350.[citado 2024 abr. 24 ]
    • Vancouver

      Donnici CL, Pereira EHT, Lopes JCD, Marzorati L, Wladislaw B. Selective sulfenylative desulfonylation or decarbalkoxylation of 'alfa'-sulfonyl malonates with dabco or 'BU IND. 3' N: reactivity and conformational analysis. Synthetic Communications. 2010 ; 40( 3): 342-350.[citado 2024 abr. 24 ]

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