Lipophilicity assessment and chromatographic characterization of new spirohydantoin derivatives potential anticonvulsant agents
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In this poster presentation the retention data of new cycloalkane-5-spirohydantoins bearing a substituted benzyl group in position 3 of the heterocyclic ring have been examined (Figure 1). Previously the intermolecular interactions of the crystal structures of
cycloalkane-S-spirohydantoins with halo-
In
geno substituted benzyl group (R = Cl and
Br) in position 3 had been studied [1].
Besides, the eflect of R substituent on the absorption UV-Vis spectra of cyclopen-tanespiro-S-hydantoins (2] had been studied,
100.
Source:
Book of Abstracts / Conferentia Chemometrica 2017, Gyöngyös-Farkasmály, Hungary, September 03-06, 2017, 2017, P09-Publisher:
- Budapest : Research Centre for Natural Sciences, Institute of Excellence, Hungarian Academy of Sciences
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Inovacioni centarTY - CONF AU - Đaković-Sekulić, Tatjana AU - Smolinski, Adam AU - Tot, Kristina AU - Lazić, Anita PY - 2017 UR - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7464 AB - In this poster presentation the retention data of new cycloalkane-5-spirohydantoins bearing a substituted benzyl group in position 3 of the heterocyclic ring have been examined (Figure 1). Previously the intermolecular interactions of the crystal structures of cycloalkane-S-spirohydantoins with halo- In geno substituted benzyl group (R = Cl and Br) in position 3 had been studied [1]. Besides, the eflect of R substituent on the absorption UV-Vis spectra of cyclopen-tanespiro-S-hydantoins (2] had been studied, 100. PB - Budapest : Research Centre for Natural Sciences, Institute of Excellence, Hungarian Academy of Sciences C3 - Book of Abstracts / Conferentia Chemometrica 2017, Gyöngyös-Farkasmály, Hungary, September 03-06, 2017 T1 - Lipophilicity assessment and chromatographic characterization of new spirohydantoin derivatives potential anticonvulsant agents SP - P09 UR - https://hdl.handle.net/21.15107/rcub_technorep_7464 ER -
@conference{ author = "Đaković-Sekulić, Tatjana and Smolinski, Adam and Tot, Kristina and Lazić, Anita", year = "2017", abstract = "In this poster presentation the retention data of new cycloalkane-5-spirohydantoins bearing a substituted benzyl group in position 3 of the heterocyclic ring have been examined (Figure 1). Previously the intermolecular interactions of the crystal structures of cycloalkane-S-spirohydantoins with halo- In geno substituted benzyl group (R = Cl and Br) in position 3 had been studied [1]. Besides, the eflect of R substituent on the absorption UV-Vis spectra of cyclopen-tanespiro-S-hydantoins (2] had been studied, 100.", publisher = "Budapest : Research Centre for Natural Sciences, Institute of Excellence, Hungarian Academy of Sciences", journal = "Book of Abstracts / Conferentia Chemometrica 2017, Gyöngyös-Farkasmály, Hungary, September 03-06, 2017", title = "Lipophilicity assessment and chromatographic characterization of new spirohydantoin derivatives potential anticonvulsant agents", pages = "P09", url = "https://hdl.handle.net/21.15107/rcub_technorep_7464" }
Đaković-Sekulić, T., Smolinski, A., Tot, K.,& Lazić, A.. (2017). Lipophilicity assessment and chromatographic characterization of new spirohydantoin derivatives potential anticonvulsant agents. in Book of Abstracts / Conferentia Chemometrica 2017, Gyöngyös-Farkasmály, Hungary, September 03-06, 2017 Budapest : Research Centre for Natural Sciences, Institute of Excellence, Hungarian Academy of Sciences., P09. https://hdl.handle.net/21.15107/rcub_technorep_7464
Đaković-Sekulić T, Smolinski A, Tot K, Lazić A. Lipophilicity assessment and chromatographic characterization of new spirohydantoin derivatives potential anticonvulsant agents. in Book of Abstracts / Conferentia Chemometrica 2017, Gyöngyös-Farkasmály, Hungary, September 03-06, 2017. 2017;:P09. https://hdl.handle.net/21.15107/rcub_technorep_7464 .
Đaković-Sekulić, Tatjana, Smolinski, Adam, Tot, Kristina, Lazić, Anita, "Lipophilicity assessment and chromatographic characterization of new spirohydantoin derivatives potential anticonvulsant agents" in Book of Abstracts / Conferentia Chemometrica 2017, Gyöngyös-Farkasmály, Hungary, September 03-06, 2017 (2017):P09, https://hdl.handle.net/21.15107/rcub_technorep_7464 .