Zobrazeno 1 - 10
of 185
pro vyhledávání: '"Bof de Oliveira A"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 80, Iss 5, Pp 452-458 (2024)
The title compound (C14H23N3S, common name: cis-jasmone 4-ethylthiosemicarbazone) was synthesized by the equimolar reaction of cis-jasmone and 4-ethylthiosemicarbazide in ethanol facilitated by acid catalysis. There is one crystallographically indepe
Externí odkaz:
https://doaj.org/article/493646ccfa734634ac2dfa403ec3a999
Autor:
Ana Paula Lopes de Melo, Leandro Bresolin, Bárbara Tirloni, Renan Lira de Farias, Adriano Bof de Oliveira
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 79, Iss 12, Pp 1166-1172 (2023)
The reaction between the (R,S)-fixolide 4-methylthiosemicarbazone and PdII chloride yielded the title compound, [Pd(C20H30N3S)2]·C2H6O {common name: trans-bis[(R,S)-fixolide 4-methylthiosemicarbazonato-κ2N2S]palladium(II) ethanol monosolvate}. The
Externí odkaz:
https://doaj.org/article/b61fca9da8674879a02aee4517fbdcaa
Autor:
Ana Paula Lopes de Melo, Bianca Barreto Martins, Leandro Bresolin, Bárbara Tirloni, Adriano Bof de Oliveira
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 79, Iss 11, Pp 993-998 (2023)
The reaction of (2E)-N-phenyl-2-[(2E)-3-phenyl-2-propen-1-ylidene]hydrazinecarbothioamide (common name: cinnamaldehyde-4-phenylthiosemicarbazone) deprotonated with NaOH in ethanol with an ethanolic suspension of PdII chloride in a 2:1 molar ratio yie
Externí odkaz:
https://doaj.org/article/b2909f2aaeb34a1ba12dc2a939a67a62
Publikováno v:
IUCrData, Vol 9, Iss 1, p x240013 (2024)
The equimolar and hydrochloric acid-catalysed reaction between cis-jasmone and 4-methylthiosemicarbazide in ethanolic solution yields the title compound, C13H21N3S (common name: cis-jasmone 4-methylthiosemicarbazone). Two molecules with all atoms in
Externí odkaz:
https://doaj.org/article/2b81569ece214f91a68189ad00b63d1a
Publikováno v:
IUCrData, Vol 9, Iss 1, p x240009 (2024)
In the paper by Oliveira et al. [IUCrData (2023), 8, x230971], there was an error in the name of the first author.
Externí odkaz:
https://doaj.org/article/0207a7882af949d98333c822bf1b1cf2
Autor:
Ana Paula Lopes de Melo, Alex Fabiani Claro Flores, Leandro Bresolin, Bárbara Tirloni, Adriano Bof de Oliveira
Publikováno v:
IUCrData, Vol 8, Iss 11, p x231020 (2023)
The reaction between a racemic mixture of (R,S)-fixolide and 4-methylthiosemicarbazide in ethanol with a 1:1 stoichiometric ratio and catalysed with HCl, yielded the title compound, C20H31N3S [common name: (R,S)-fixolide 4-methylthiosemicarbazone]. T
Externí odkaz:
https://doaj.org/article/adeec56e5ee94795a5db1a25681bd1a9
Autor:
Adriano Bof de Oliveira, Leandro Bresolin, Vanessa Carratu Gervini, Johannes Beck, Jörg Daniels
Publikováno v:
IUCrData, Vol 8, Iss 11, p x231018 (2023)
A second crystalline modification of the title compound, C12H19N3S [common name: cis-jasmone thiosemicarbazone] was crystallized from tetrahydrofurane at room temperature. There is one crystallographic independent molecule in the asymmetric unit, sho
Externí odkaz:
https://doaj.org/article/caed76b8b5434ed1b252fa9f00c72e8d
Autor:
Fabrício Carvalho Pires, Leandro Bresolin, Vanessa Carratu Gervini, Bárbara Tirloni, Adriano Bof de Oliveira
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 1, Pp 115-120 (2020)
The equimolar reaction between a racemic mixture of (R)- and (S)-camphorquinone with thiosemicarbazide yielded the title compound, C11H17N3OS [common name: (R)- and (S)-camphor thiosemicarbazone], which maintains the chirality of the methylated chira
Externí odkaz:
https://doaj.org/article/809965a0a03a4fe08619f590c9cf74a3
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications; Apr2024, Vol. 80 Issue 5, p152-158, 12p
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 11, Pp 1547-1552 (2018)
The reaction between 4,5,6,7-tetrahydro-2-(4,5,6,7-tetrahydro-1,3-benzodithiol-2-ylidene)-1,3-benzodithiole (common name: 4,4′,5,5′,6,6′,7,7′-octahydrodibenzotetrathiafulvalene, OMTTF) and an excess of iodine in tetrahydrofuran (THF) yielded
Externí odkaz:
https://doaj.org/article/c6219330e1be4dfdbdd80bbba1a12ad9