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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: 06 nov. 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 nov. 06 ] 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 nov. 06 ] 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: 06 nov. 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 nov. 06 ] 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 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
Artigo de periodico
Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids (2010)
Stefani, Hélio Alexandre ; Amaral, Monica Franco Zanini Junqueira; Reyes-Rangel, Gloria; Vargas-Caporali, Jorge; Juaristi, Eusebio
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: AMINOÁCIDOS, PALÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids. European Journal of Organic Chemistry, v. 2010, n. 33, p. 6393-6403, 2010Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201000852. Acesso em: 06 nov. 2024.
APA
Stefani, H. A., Amaral, M. F. Z. J., Reyes-Rangel, G., Vargas-Caporali, J., & Juaristi, E. (2010). Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids. European Journal of Organic Chemistry, 2010( 33), 6393-6403. doi:10.1002/ejoc.201000852
NLM
Stefani HA, Amaral MFZJ, Reyes-Rangel G, Vargas-Caporali J, Juaristi E. Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 33): 6393-6403.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/ejoc.201000852
Vancouver
Stefani HA, Amaral MFZJ, Reyes-Rangel G, Vargas-Caporali J, Juaristi E. Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts: convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids [Internet]. European Journal of Organic Chemistry. 2010 ; 2010( 33): 6393-6403.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/ejoc.201000852

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