Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 959283

PREPARATION OF FERROCENOYL-NUCLEOBASE CONJUGATES BY ONE-STEP SYNTHETIC ROUTE


Djaković, Senka; Filipović, Alma; Toma, Mateja; Lapić, Jasmina; Šakić, Davor; Vrček, Valerije
PREPARATION OF FERROCENOYL-NUCLEOBASE CONJUGATES BY ONE-STEP SYNTHETIC ROUTE // Book of abstracts, International conference 17th Ružička Days "Today Science-Tomorrow Industry" / Tomas, Srećko ; Ačkar, Đurđica (ur.).
Osijek: Prehrambeno tehnološki fakultet Sveučilišta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2018. str. 30-30 (predavanje, domaća recenzija, sažetak, znanstveni)


CROSBI ID: 959283 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
PREPARATION OF FERROCENOYL-NUCLEOBASE CONJUGATES BY ONE-STEP SYNTHETIC ROUTE

Autori
Djaković, Senka ; Filipović, Alma ; Toma, Mateja ; Lapić, Jasmina ; Šakić, Davor ; Vrček, Valerije

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Book of abstracts, International conference 17th Ružička Days "Today Science-Tomorrow Industry" / Tomas, Srećko ; Ačkar, Đurđica - Osijek : Prehrambeno tehnološki fakultet Sveučilišta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2018, 30-30

ISBN
978-953-7005-57-3

Skup
17. Ružičkini dani "Danas znanost - sutra industrija"

Mjesto i datum
Vukovar, Hrvatska, 19.09.2018. - 21.09.2018

Vrsta sudjelovanja
Predavanje

Vrsta recenzije
Domaća recenzija

Ključne riječi
ferrocenoyl-nucleobase conjugate, regioselectivity, biological activity

Sažetak
Nucleosides are a large family of natural compounds and their chemically modified analogs, which are characterized by great structural diversity. The sugar unit in these molecules is frequently modified (e.g. in AZT or gemcitabine) or completely replaced (e.g. in abacovir and acyclovir) [1]. Due to its stability, ease of functionalisation and potential for novel modes of action through its redox properties, ferrocene has been in the centre of bioorganometallic medicinal chemistry field [2]. Preparation of ferrocene nucleobase derivatives is based on synthetic copulation of the organometallic moiety and the heterocyclic base using the carbonyl group as the bridge [3]. Our focus in this research is on preparation of a series of novel ferrocene-modified nucleobases from nucleobases and ferrocenoyl chloride by one-step method. The ferrocenoyl units have been successfully introduced into different N- positions of the purine (type I and II) and pyrimidine (type III) ring systems (Figure 1). The position of substitution in products and the reaction regioselectivity will be explored by spectroscopy methods (1D and 2D-NMR, FTIR) and quantum chemical calculations (DFT level of theory).

Izvorni jezik
Engleski

Znanstvena područja
Kemija, Farmacija



POVEZANOST RADA


Projekti:
HRZZ-IP-2016-06-1137 - Kvantno-kemijski dizajn, priprava i biološka svojstva organometalnih derivata nukleobaza (OrDeN) (Vrček, Valerije, HRZZ - 2016-06) ( CroRIS)

Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Prehrambeno-biotehnološki fakultet, Zagreb


Citiraj ovu publikaciju:

Djaković, Senka; Filipović, Alma; Toma, Mateja; Lapić, Jasmina; Šakić, Davor; Vrček, Valerije
PREPARATION OF FERROCENOYL-NUCLEOBASE CONJUGATES BY ONE-STEP SYNTHETIC ROUTE // Book of abstracts, International conference 17th Ružička Days "Today Science-Tomorrow Industry" / Tomas, Srećko ; Ačkar, Đurđica (ur.).
Osijek: Prehrambeno tehnološki fakultet Sveučilišta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2018. str. 30-30 (predavanje, domaća recenzija, sažetak, znanstveni)
Djaković, S., Filipović, A., Toma, M., Lapić, J., Šakić, D. & Vrček, V. (2018) PREPARATION OF FERROCENOYL-NUCLEOBASE CONJUGATES BY ONE-STEP SYNTHETIC ROUTE. U: Tomas, S. & Ačkar, Đ. (ur.)Book of abstracts, International conference 17th Ružička Days "Today Science-Tomorrow Industry".
@article{article, author = {Djakovi\'{c}, Senka and Filipovi\'{c}, Alma and Toma, Mateja and Lapi\'{c}, Jasmina and \v{S}aki\'{c}, Davor and Vr\v{c}ek, Valerije}, year = {2018}, pages = {30-30}, keywords = {ferrocenoyl-nucleobase conjugate, regioselectivity, biological activity}, isbn = {978-953-7005-57-3}, title = {PREPARATION OF FERROCENOYL-NUCLEOBASE CONJUGATES BY ONE-STEP SYNTHETIC ROUTE}, keyword = {ferrocenoyl-nucleobase conjugate, regioselectivity, biological activity}, publisher = {Prehrambeno tehnolo\v{s}ki fakultet Sveu\v{c}ili\v{s}ta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko dru\v{s}tvo kemijskih in\v{z}enjera i tehnologa (HDKI)}, publisherplace = {Vukovar, Hrvatska} }
@article{article, author = {Djakovi\'{c}, Senka and Filipovi\'{c}, Alma and Toma, Mateja and Lapi\'{c}, Jasmina and \v{S}aki\'{c}, Davor and Vr\v{c}ek, Valerije}, year = {2018}, pages = {30-30}, keywords = {ferrocenoyl-nucleobase conjugate, regioselectivity, biological activity}, isbn = {978-953-7005-57-3}, title = {PREPARATION OF FERROCENOYL-NUCLEOBASE CONJUGATES BY ONE-STEP SYNTHETIC ROUTE}, keyword = {ferrocenoyl-nucleobase conjugate, regioselectivity, biological activity}, publisher = {Prehrambeno tehnolo\v{s}ki fakultet Sveu\v{c}ili\v{s}ta Josipa Jurja Strossmayera u Osijeku ; Hrvatsko dru\v{s}tvo kemijskih in\v{z}enjera i tehnologa (HDKI)}, publisherplace = {Vukovar, Hrvatska} }




Contrast
Increase Font
Decrease Font
Dyslexic Font