Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Laura G. Sârbu"'
Autor:
Elena Matei, Lucian M. Bîrsă, Mădălina I. Duinea, Florinel Sava, Laura G. Sârbu, Paul Chiriţă, Mihaela Baibarac
Publikováno v:
Transactions of Nonferrous Metals Society of China. 30:1928-1942
The effects of 4-(2-hydroxyphenyl)-2-(morpholin-4-yl)-1,3-thiazole (Pr02), 1-(3,5-dibromo-2-hydroxyphenyl)- 1-oxoethan-2-yl-N,N-diethyldithiocarbamate (Pr04) and 1-(5-bromo-2-hydroxy-3-methylphenyl)-1-oxoethan-2-yl-O- ethyl xanthate (Pr06) on the aqu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92f65a39848a63c8f693cb4b3129eef9
https://doi.org/10.1016/s1003-6326(20)65351-1
https://doi.org/10.1016/s1003-6326(20)65351-1
Autor:
Laura G. Sârbu, Mădălina I. Duinea, Paul Chiriţă, Lucian M. Birsa, Elena Matei, Mihai Popescu, Florinel Sava, Ana M. Sandu, Mihaela Baibarac
Publikováno v:
Corrosion Science. 138:154-162
Three phenacyl derivatives have been investigated as potential inhibitors for the aqueous oxidation of sphalerite (ZnS) in air-equilibrated solutions of HCl (pH 2.5 and 25 °C) using potentyodynamic polarization, aqueous batch experiments, scanning e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95324594a314204af22763d9090454f5
https://doi.org/10.1016/j.corsci.2018.04.017
https://doi.org/10.1016/j.corsci.2018.04.017
Autor:
Mihail Lucian Birsa, Laura G. Sarbu
Publikováno v:
Molecules, Vol 27, Iss 23, p 8430 (2022)
The synthesis of new iodine containing synthetic tricyclic flavonoids is reported. Due to the sensitivity of the precursors to the heat and acidic conditions required for the ring closure of the 1,3-dithiolium core, a new cyclization method has been
Externí odkaz:
https://doaj.org/article/3a09e482d89d4da99877db41842b2c90
Publikováno v:
ARKIVOC, Vol 2019, Iss 6, Pp 174-179 (2019)
Externí odkaz:
https://doaj.org/article/c0b28e7059c8494f814e1feb3f1e9580
Autor:
Lucian G. Bahrin, Henning Hopf, Peter G. Jones, Laura G. Sarbu, Cornelia Babii, Alina C. Mihai, Marius Stefan, Lucian M. Birsa
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1065-1071 (2016)
A structure–activity relationship study concerning the antibacterial properties of several halogen-substituted tricyclic sulfur-containing flavonoids has been performed. The compounds have been synthesized by cyclocondensation of the corresponding
Externí odkaz:
https://doaj.org/article/e030234a73e14c25a76d7c1914517085
Publikováno v:
Molecules, Vol 25, Iss 22, p 5262 (2020)
The synthesis of paracyclophane-based tetrathiafulvalene precursors is described in the context of the importance of these compounds in the field of material chemistry. Pseudo-geminal bis(1,3-dithia-2-thione) was synthesized via the corresponding 1,3
Externí odkaz:
https://doaj.org/article/df7a5cf13cf1462b854f2bcc615fb6df
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1917-1921 (2015)
The synthesis of [2.2]paracyclophane derivatives containing tetrathiafulvalene units has been accomplished by the coupling reaction of 4-([2.2]paracyclophan-4-yl)-1,3-dithiol-2-thione in the presence of trimethylphosphite. The 1,3-dithiol-2-thione de
Externí odkaz:
https://doaj.org/article/d98dc107f7a545419a6d50092b3b4a44
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2550-2555 (2014)
An addition/elimination sequence of selenium halides to pseudo-geminally bis(acetylene) substituted [2.2]paracyclophanes leads to new bridges with an endo-exo-diene substructure. The reactions have been found to be sensitive to the substitution of th
Externí odkaz:
https://doaj.org/article/86cefad4859048198018070f14d69df5
Autor:
Laura G. Sarbu, Sergiu Shova, Dragos Peptanariu, Isabela A. Sandu, Lucian M. Birsa, Lucian G. Bahrin
Publikováno v:
Molecules, Vol 24, Iss 13, p 2459 (2019)
Background: Due to the emergence of multidrug resistant microorganisms, new classes of antibiotics are needed. In this paper, we present the cytotoxic effects of five tricyclic flavonoids, one of which was previously identified as a potent antimicrob
Externí odkaz:
https://doaj.org/article/81b19fedd9df4041b5fac3518fbb27f6
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 7, Pp o1169-o1169 (2013)
In the racemic title compound, C14H16BrNO3S2, synthesized from the corresponding ω-bromopropiophenone, the dihedral angle between the plane of the phenol group and that of the planar section [maximum deviation = 0.040 (2) Å] of the morpholine-4-car
Externí odkaz:
https://doaj.org/article/e2f5c12aaad4468f95f0324890f4b07e